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(+-)-11-hydroxy-DELTA9-tetrahydrocannabinol + UDP-glucuronate
? + UDP
-
Substrates: substrate for isoforms UGT1A9 and UGT1A10
Products: -
?
(-)-11-nor-9-carboxy-DELTA9-tetrahydrocannabinol + UDP-glucuronate
? + UDP
-
Substrates: substrate for isoforms UGT1A1 and UGT1A3, no substrate for UGT1A9 and UGT1A10
Products: -
?
(R)-6-hydroxywarfarin + UDP-alpha-D-glucuronate
(R)-6-hydroxywarfarin 6-O-beta-D-glucuronide + UDP
-
Substrates: -
Products: -
?
(R)-7-hydroxywarfarin + UDP-alpha-D-glucuronate
(R)-7-hydroxywarfarin 7-O-beta-D-glucuronide + UDP
-
Substrates: -
Products: -
?
(R)-8-hydroxywarfarin + UDP-alpha-D-glucuronate
(R)-8-hydroxywarfarin 8-O-beta-D-glucuronide + UDP
-
Substrates: -
Products: -
?
(R)-propanolol + UDP-glucuronate
UDP + (R)-propanolol O-glucuronide
-
Substrates: -
Products: -
?
(S)-6-hydroxywarfarin + UDP-alpha-D-glucuronate
(S)-6-hydroxywarfarin 6-O-beta-D-glucuronide + UDP
-
Substrates: -
Products: -
?
(S)-7-hydroxywarfarin + UDP-alpha-D-glucuronate
(S)-7-hydroxywarfarin 7-O-beta-D-glucuronide + UDP
-
Substrates: -
Products: -
?
(S)-8-hydroxywarfarin + UDP-alpha-D-glucuronate
(S)-8-hydroxywarfarin 8-O-beta-D-glucuronide + UDP
-
Substrates: -
Products: -
?
(S)-naproxen + UDP-alpha-D-glucuronate
beta-D-glucuronosyl (S)-naproxen + UDP
-
Substrates: -
Products: -
?
(S)-naproxen + UDP-alpha-D-glucuronate
UDP + beta-D-glucuronosyl (S)-naproxen
-
Substrates: -
Products: -
?
(S)-oxazepam + UDP-glucuronate
UDP + (S)-oxazepam beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, P35503, P54855, O75795, P06133, P36537, P35504 Substrates: -
Products: -
?
(S)-propanolol + UDP-glucuronate
UDP + (S)-propanolol O-glucuronide
-
Substrates: -
Products: -
?
1-hydroxy-benzo(a)pyrene + UDP-glucuronate
1-hydroxy-benzo(a)pyrene 1-O-glucuronate + UDP
-
Substrates: -
Products: -
?
1-hydroxy-benzo[a]pyrene + UDP-D-glucose
benzo[a]pyrenil-1-O-D-glucoside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
1-hydroxy-pyrene + UDP-D-xylose
pyrene 1-O-D-xyloside + UDP
Substrates: -
Products: -
?
1-hydroxybenzo(a)pyrene + UDP-glucuronate
?
1-hydroxypyrene + UDP-D-glucose
pyrene 1-O-D-glucoside + UDP
Substrates: -
Products: -
?
1-hydroxypyrene + UDP-glucuronate
1-hydroxypyrene 1-O-glucuronate + UDP
-
Substrates: -
Products: -
?
1-hydroxypyrene + UDP-glucuronate
?
Substrates: -
Products: -
?
1-hydroxypyrene + UDP-glucuronate
pyrene 1-O-glucuronide + UDP
Substrates: -
Products: -
?
1-hydroxypyrene + UDP-N-acetylglucosamine
pyrenil-1-O-(N-acetylglucosaminide) + UDP
Substrates: activity of only UGT3A1-overexpressing microsomes, not wild-type cell microsomes
Products: -
?
1-hydroxy[a]pyrene + UDP-glucuronate
UDP + benzo[a]pyren-1-yl-alpha-D-glucuronide
Substrates: -
Products: -
?
1-naphthol + UDP-alpha-D-glucuronate
1-naphthyl-O-glucuronide + UDP
-
Substrates: -
Products: -
?
1-naphthol + UDP-D-glucose
naphthyl-1-O-D-glucoside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
1-naphthol + UDP-glucuronate
1-naphthyl 1-O-glucuronate + UDP
-
Substrates: -
Products: -
?
1-naphthol + UDP-glucuronate
1-naphthyl-O-glucuronide + UDP
Substrates: -
Products: -
?
1-naphthol + UDP-glucuronate
?
Substrates: -
Products: -
?
1-naphthol + UDP-glucuronate
naphth-1-yl-beta-D-glucuronide + UDP
-
Substrates: -
Products: -
?
1-naphthol + UDP-glucuronate
UDP + naphth-1-yl-beta-D-glucuronide
11alpha-hydroxyprogesterone + UDP-glucuronate
UDP + 11alpha-hydroxyprogesterone-11-O-D-glucuronate
Substrates: -
Products: -
?
12-hydroxybenzo[a]pyrene + UDP-glucuronate
UDP + benzo[a]pyren-12-yl-beta-D-glucuronide
-
Substrates: glucuronidated by UGT1A3, inactive towards benz[a]pyrene trans 4,5 and 7,8 dihydrodiols
Products: -
?
12-hydroxyeicosatetraenoic acid + UDP-glucuronate
?
Substrates: -
Products: -
?
13-hydroxyoctadecadienoic acid + UDP-glucuronate
?
Substrates: -
Products: -
?
16alpha-hydroxyprogesterone + UDP-glucuronate
?
16alpha-hydroxyprogesterone + UDP-glucuronate
UDP + 16alpha-hydroxyprgesterone-16-O-D-glucuronate
17-epiestriol + UDP-glucuronate
?
Substrates: -
Products: -
?
17-epiestriol + UDP-glucuronate
UDP + ?
-
Substrates: -
Products: -
?
17alpha-estradiol + UDP-alpha-D-glucuronate
? + UDP
-
Substrates: -
Products: -
?
17beta-estradiol + UDP-alpha-D-glucuronate
? + UDP
-
Substrates: -
Products: -
?
17beta-estradiol + UDP-glucuronate
?
Substrates: metabilized by mutant enzyme S432G-UGT1A7, but not by wild-type enzyme UGT1A7
Products: -
?
2 UDP-D-glucuronate + 2 dexmedetomidine
2 UDP + dexmedetomidine N1-beta-D-glucuronoside + dexmedetomidine N3-beta-D-glucuronoside
2 UDP-D-glucuronate + 2 levomedetomidine
2 UDP + levomedetomidine N1-beta-D-glucuronoside + dexmedetomidine N3-beta-D-glucuronoside
2',4,4'-trihydroxychalcone + UDP-glucuronate
UDP + 2',4,4'-trihydroxychalcone 4'-O-glucoside + 2',4,4'-trihydroxychalcone 2'-O-glucoside
-
Substrates: i.e. isoliquiritigenin
Products: -
?
2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid + UDP-glucuronate
?
2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid + UDPglucuronate
?
Substrates: glucuronidation of 2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid is mainly catalyzed by UGT1A1, UGT1A9, and UGT2B7 in the liver, and by UGT1A1, UGT1A3, and UGT2B7 in the intestine in humans
Products: -
?
2-aminobiphenyl + UDP-glucuronate
?
Substrates: -
Products: -
?
2-hydroxyestradiol + UDP-glucuronate
?
Substrates: -
Products: -
?
2-hydroxyestradiol + UDPglucuronate
UDP + 2-hydroxyestradiol O-glucuronide
2-hydroxyestrone + UDP-glucuronate
?
Substrates: -
Products: -
?
2-hydroxyestrone + UDPglucuronate
2-hydroxyestrone 2-O-glucuronide + UDP
21-hydroxyprogesterone + UDP-glucuronate
UDP + 21-hydroxyprogesterone-21-O-D-glucuronate
Substrates: -
Products: -
?
3 quercetin + 3 UDP-glucuronate
3 UDP + quercetin 7-glucuronide + quercetin 3-glucuronide + quercetin 3'-glucuronide
Substrates: isoform UGT1A9 mainly converts quercetin into three monoglucuronides, including 7-glucuronide, 3-glucuronide, and 3'-glucuronide
Products: -
?
3'-azido-3'-deoxythymidine + UDP-alpha-D-glucuronate
3'-azido-3'-deoxythymidine 5'-O-glucuronide + UDP
-
Substrates: substrate of isoform UGT2B7
Products: -
?
3'-azido-3'-deoxythymidine + UDPglucuronate
3'-azido-3'-deoxythymidine 5'-O-glucuronide + UDP
-
Substrates: -
Products: -
?
3-azido-4-chlorobenzoic acid + UDP-glucuronate
?
Substrates: -
Products: -
?
3-azidobenzoic acid + UDP-glucuronate
?
Substrates: -
Products: -
?
3-hydroxy-benzo(a)pyrene + UDP-glucuronate
3-hydroxy-benzo(a)pyrene 3-O-glucuronate + UDP
-
Substrates: -
Products: -
?
3-hydroxy-benzo[a]pyrene + UDP-D-glucose
benzo[a]pyrenil-3-O-D-glucoside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
3-hydroxybenzo(a)pyrene + UDP-glucuronate
?
3-hydroxybenzo[a]pyrene + UDPglucuronate
UDP + 3-hydroxybenzo[a]pyrene-O-glucuronide
-
Substrates: -
Products: -
?
3-hydroxydesloratadine + UDP-glucuronate
UDP + 3-hydroxydesloratadinyl-O-glucuronide
4-aminobiphenyl + UDP-glucuronate
UDP + 4-aminobiphenyl N-glucuronide
-
Substrates: -
Products: -
?
4-aminobiphenyl + UDPglucuronate
UDP + ?
-
Substrates: catalyzed by isozyme 1 but not by isozyme 2
Products: -
?
4-azido-2-hydroxybenzoic acid + UDPglucuronate
?
Substrates: -
Products: -
?
4-azidobenzoic acid + UDP-glucuronate
?
Substrates: -
Products: -
?
4-hydroxybiphenyl + UDP-glucuronate
UDP + 4-hydroxybiphenyl 4-O-beta-D-glucuronide
4-hydroxyestradiol + UDP-glucuronate
?
Substrates: -
Products: -
?
4-hydroxyestradiol + UDPglucuronate
UDP + 4-hydroxyestradiol O-glucuronide
4-hydroxyestrone + UDP-glucuronate
?
4-hydroxyestrone + UDP-glucuronate
UDP + 4-hydroxyestrone 4-O-glucuronide
4-hydroxyestrone + UDP-glucuronate
UDP + 4-hydroxyestrone-4-O-beta-D-glucuronide
-
Substrates: -
Products: -
?
4-methylumbeliferone + UDP-alpha-D-glucuronate
4-methylumbelliferyl-7-O-alpha-D-glucuronide
4-methylumbeliferone + UDP-glucuronate
4-methylumbelliferyl-7-O-beta-D-glucuronide
-
Substrates: -
Products: -
?
4-methylumbelliferone + UDP-glucuronate
UDP + 4-methylumbelliferyl beta-D-glucuronide
4-methylumbelliferone + UDP-glucuronate
UDP + 4-methylumbelliferyl-7-O-beta-D-glucuronide
4-methylumbelliferone + UDP-glucuronate
UDP + 4-methylumbelliferyl-beta-D-glucuronide
-
Substrates: -
Products: -
?
4-nitrophenol + UDP-glucuronate
4-nitrophenyl beta-D-glucuronide + UDP
5-diethylaminoethylamino-8-hydroxyimidazoacridinone + UDP-alpha-D-glucuronate
5-{[2-(diethylamino)ethyl]amino}-6-oxo-6H-imidazo[4,5,1-de]acridin-8-yl beta-D-glucuronide + UDP
-
Substrates: i.e. antitumor agent C-1311, NSC-645809
Products: -
?
5-dimethylaminopropylamino-8-hydroxytriazoloacridinone + UDP-alpha-D-glucuronate
5-dimethylaminopropylamino-8-hydroxytriazoloacridinone-8-D-glucuronide + UDP
-
Substrates: i.e. antitumor agent C-1305
Products: -
?
5-hydroxybenzo[a]pyrene + UDPglucuronate
UDP + 5-hydroxybenzo[a]pyrene O-glucuronide
-
Substrates: glucuronidated by UGT1A3
Products: -
?
5-hydroxyrofecoxib + UDP-glucuronate
UDP + 5-hydroxyrofecoxib beta-D-glucuronide
Substrates: -
Products: -
?
5-methylchrysene-1,2-diol + UDP-D-glucose
1-hydroxy-5-methylchrysene-2-O-D-glucoside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
5-methylchrysene-1,2-diol + UDP-D-glucose
2-hydroxy-5-methylchrysene-1-O-D-glucoside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
5-methylchrysene-1,2-diol + UDP-D-xylose
1-hydroxy-5-methylchrysene-2-O-D-xyloside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
5-methylchrysene-1,2-diol + UDP-D-xylose
2-hydroxy-5-methylchrysene-1-O-D-xyloside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
5-methylchrysene-1,2-diol + UDP-glucuronate
? + UDP
-
Substrates: -
Products: -
?
5alpha-androstane-3alpha,17beta-diol + UDP-glucuronate
?
Substrates: -
Products: -
?
5alpha-androstane-3alpha,17beta-diol + UDP-glucuronate
UDP + 5alpha-androstane-3alpha,17beta-diol O-glucuronide
6-hydroxywarfarin + UDP-glucuronate
? + UDP
-
Substrates: -
Products: -
?
6alpha-hydroxyprogesterone + UDP-glucuronate
UDP + 6alpha-hydroxyprogesteron-6-O-alpha-D-glucuronate
Substrates: -
Products: -
?
7-ethyl-10-hydroxy-camptothecin + UDP-glucuronate
UDP + 7-ethyl-10-hydroxy-camptothecin beta-D-glucuronide
Substrates: i.e SN-38, substrate for isoform UGT1A1
Products: -
?
7-ethyl-10-hydroxy-camptothecin carboxylate + UDP-glucuronate
UDP + 7-ethyl-camptothecin carboxylate-10-yl-beta-D-glucuronate
Substrates: -
Products: -
?
7-ethyl-10-hydroxy-camptothecin lactone + UDP-glucuronate
UDP + 7-ethyl-camptothecin lactone-10-yl-beta-D-glucuronate
Substrates: -
Products: -
?
7-ethyl-10-hydroxycamptothecin + UDP-alpha-D-glucuronate
7-ethyl-10-hydroxycamptothecin 10-O-glucuronate + UDP
Substrates: -
Products: -
?
7-hydroxy benzo(a)pyrene + UDP-glucuronate
?
7-hydroxy-4-trifluoromethylcoumarin + UDP-alpha-D-glucuronate
7-hydroxy-4-trifluoromethylcoumarin 7-O-glucuronate + UDP
Substrates: -
Products: -
?
7-hydroxy-4-trifluoromethylcoumarin + UDP-glucuronate
UDP + 7-hydroxy-4-trifluoromethylcoumarin beta-D-glucuronide
7-hydroxy-benzo(a)pyrene + UDP-glucuronate
7-hydroxy-benzo(a)pyrene 7-O-glucuronate + UDP
-
Substrates: -
Products: -
?
7-hydroxy-benzo[a]pyrene + UDP-D-glucose
benzo[a]pyrenil-7-O-D-glucoside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
7-hydroxywarfarin + UDP-glucuronate
? + UDP
-
Substrates: -
Products: -
?
8-hydroxy-benzo(a)pyrene + UDP-glucuronate
8-hydroxy-benzo(a)pyrene 8-O-glucuronate + UDP
-
Substrates: -
Products: -
?
8-hydroxy-benzo[a]pyrene + UDP-glucuronate
benzo[a]pyrenil-8-O-glucuronide + UDP
Substrates: activity of only UGT3A1-overexpressing microsomes, not wild-type cell microsomes
Products: -
?
8-hydroxywarfarin + UDP-glucuronate
? + UDP
-
Substrates: -
Products: -
?
9-hydroxy-benzo[a]pyrene + UDP-D-glucose
benzo[a]pyrenil-9-O-D-glucoside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
9-hydroxybenzo(a)pyrene + UDP-glucuronate
?
acetaminophen + UDP-glucuronate
?
acetaminophen + UDP-glucuronate
UDP + ?
P16662, P19224, O60656, P22309, P22310, P35503, P54855, O75795, P06133, P36537, P35504 Substrates: -
Products: -
?
acetaminophen + UDP-glucuronate
UDP + acetaminophen beta-D-glucuronate
-
Substrates: -
Products: -
?
alpha-naphthylamine + UDPglucuronate
UDP + ?
-
Substrates: -
Products: -
?
alprazolam + UDP-alpha-D-glucuronate
alprazolam D-glucuronate + UDP
-
Substrates: -
Products: -
?
amitriptyline + UDP-glucuronate
?
Substrates: -
Products: -
?
anastrozole + UDP-glucuronate
UDP + ?
P16662, P19224, O60656, P22309, P22310, P35503, P54855, O75795, P06133, P36537, P35504 Substrates: -
Products: -
?
androsterone + UDPglucuronate
UDP + androsterone O-glucuronide
anthraflavic acid + UDPglucuronate
UDP + ?
apigenin + UDPglucuronate
UDP + apigenin O-glucuronide
-
Substrates: -
Products: -
?
bakuchiol + UDP-glucuronate
UDP + bakuchiol beta-D-glucuronide
benzo(a)pyrene-7,8-diol + UDP-glucuronate
? + UDP
-
Substrates: -
Products: -
?
benzo[a]pyrene-7,8-diol + UDP-D-glucose
7-hydroxy-benzo[a]pyrene-8-O-D-glucoside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
benzo[a]pyrene-7,8-diol + UDP-D-glucose
8-hydroxy-benzo[a]pyrene-7-O-D-glucoside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
benzo[a]pyrene-7,8-diol + UDP-D-xylose
7-hydroxy-benzo[a]pyrene-8-O-D-xyloside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
benzo[a]pyrene-7,8-diol + UDP-D-xylose
8-hydroxy-benzo[a]pyrene-7-O-D-xyloside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
benzo[a]pyrene-9,10-diol + UDP-D-glucose
10-hydroxy-benzo[a]pyrene-9-O-D-glucoside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
benzo[a]pyrene-9,10-diol + UDP-D-glucose
9-hydroxy-benzo[a]pyrene-10-O-D-glucoside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
benzo[a]pyrene-9,10-diol + UDP-D-xylose
10-hydroxy-benzo[a]pyrene-9-O-D-xyloside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
benzo[a]pyrene-9,10-diol + UDP-D-xylose
9-hydroxy-benzo[a]pyrene-10-O-D-xyloside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
benzo[a]pyrene-9,10-diol + UDP-glucuronate
10-hydroxy-benzo[a]pyrene-9-O-glucuronide + UDP
Substrates: activity of only UGT3A1-overexpressing microsomes, not wild-type cell microsomes
Products: -
?
benzo[a]pyrene-9,10-diol + UDP-glucuronate
9-hydroxy-benzo[a]pyrene-10-O-glucuronide + UDP
Substrates: activity of only UGT3A1-overexpressing microsomes, not wild-type cell microsomes
Products: -
?
benzo[a]pyrene-9,10-diol + UDP-N-acetylglucosamine
10-hydroxybenzo[a]pyrene 9-O-(N-acetylglucosaminide) + UDP
Substrates: activity of only UGT3A1-overexpressing microsomes, not wild-type cell microsomes
Products: -
?
benzo[a]pyrene-9,10-diol + UDP-N-acetylglucosamine
9-hydroxybenzo[a]pyrene 10-O-(N-acetylglucosaminide) + UDP
Substrates: activity of only UGT3A1-overexpressing microsomes, not wild-type cell microsomes
Products: -
?
beta-estradiol + UDP-alpha-D-glucuronate
beta-estradiol-3-glucuronide + UDP
-
Substrates: -
Products: -
?
beta-estradiol + UDP-glucuronate
UDP + beta-estradiol 3-O-beta-D-glucuronoside
Substrates: -
Products: -
?
beta-estradiol + UDP-glucuronate
UDP + beta-estradiol 3-O-glucuronide
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P06133, A0A0G2JMZ5, D6RH08 Substrates: -
Products: -
?
beta-estradiol + UDP-glucuronate
UDP + beta-estradiol-3-glucuronide
beta-estradiol + UDPglucuronate
beta-estradiol-3-glucuronide + UDP
-
Substrates: inactive
Products: -
?
bifonazole + UDP-alpha-D-glucuronate
bifonazole D-glucuronate + UDP
-
Substrates: -
Products: -
?
bilirubin + UDP-glucuronate
?
Substrates: -
Products: -
?
bilirubin + UDP-glucuronate
bilirubin D-glucuronate + UDP
-
Substrates: -
Products: -
?
bilirubin + UDP-glucuronate
bilirubin glucuronoside + UDP
Substrates: UGT1A1 exhibits the highest tranilast glucuronosyltransferase activity (13.5 pmol/min/mg protein)
Products: -
?
bilirubin + UDP-glucuronate
UDP + bilirubin-glucuronoside
P16662, P19224, O60656, P22309, P22310, P35503, P54855, O75795, P06133, P36537, P35504 Substrates: -
Products: -
?
bilirubin + UDPglucuronate
bilirubin monoglucuronoside + bilirubin diglucuronoside + UDP
bilirubin + UDPglucuronate
UDP + bilirubin O-glucuronide
-
Substrates: -
Products: -
?
borneol + UDPglucuronate
UDP + borneol O-glucuronide
buprenorphine + UDPglucuronate
UDP + buprenorphine O-glucuronide
-
Substrates: -
Products: -
?
C-1748 + UDP-glucuronate
UDP + C-1748 O-glucuronide
cannabinol + UDP-glucuronate
? + UDP
-
Substrates: substrate for hepatic isoform UGT1A9 and extrahepatic UGT1A7, UGT1A8, and UGT1A10
Products: -
?
carvacrol + UDP-glucuronate
caervcrol O-glucuronate + UDP
-
Substrates: isoform UGT1A9 is the major isozyme responsible for glucuronidation in liver microsomes, and isoform UGT1A7 plays a major role for glucuronidation in intestinal microsomes
Products: -
?
chenodeoxycholic acid + UDP-glucuronate
UDP + ?
chenodeoxycholic acid + UDP-glucuronate
UDP + chenodeoxycholic acid 24-acyl-beta-D-glucuronide
Substrates: -
Products: -
?
chenodeoxycholic acid + UDP-glucuronate
UDP + chenodeoxycholic acid 24-beta-D-glucuronoside
Substrates: -
Products: -
?
cholic acid + UDPglucuronate
cholic acid O-glucuronide
-
Substrates: -
Products: -
?
clofibrate + UDPglucuronate
UDP + ?
-
Substrates: glucuronidated by UGT2B7
Products: -
?
codeine + UDPglucuronate
codeine-6-glucuronide + UDP
-
Substrates: glucuronidated by HGT2B7H and HGT2B7Y
Products: -
?
deferiprone + UDP-glucuronate
deferiprone 3-O-glucuronide + UDP
-
Substrates: -
Products: -
?
deoxycholic acid + UDPglucuronate
UDP + deoxycholic acid O-glucuronide
-
Substrates: -
Products: -
?
dibenzo(a,l)pyrene-11,12-diol + UDP-glucuronate
? + UDP
-
Substrates: -
Products: -
?
dibenzo[a,1]pyrene-11,12-diol + UDP-D-glucose
11-hydroxy-benzo[a]pyrene-12-O-D-glucoside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
dibenzo[a,1]pyrene-11,12-diol + UDP-D-glucose
12-hydroxy-benzo[a]pyrene-11-O-D-glucoside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
dibenzo[a,1]pyrene-11,12-diol + UDP-D-xylose
11-hydroxy-benzo[a]pyrene-12-O-D-xyloside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
dibenzo[a,1]pyrene-11,12-diol + UDP-D-xylose
12-hydroxy-benzo[a]pyrene-11-O-D-glucoside + UDP
Substrates: UGT3A2-overexpressing microsomes
Products: -
?
diclofenac + UDP-alpha-D-glucuronate
diclofenac D-glucuronide + UDP
-
Substrates: -
Products: -
?
diclofenac + UDPalpha-D-glucuronate
UDP + ?
-
Substrates: UGT2B7 active at high rate, recombinant UGT1A9 active at moderate rate, UGT1A6 and UGT2B15 active at low rates
Products: -
?
dihydrotestosterone + UDP-alpha-D-glucuronate
dihydrotestosterone D-glucuronate + UDP
-
Substrates: -
Products: -
?
econazole + UDP-alpha-D-glucuronate
econazole D-glucuronate + UDP
-
Substrates: -
Products: -
?
edaravone + UDP-alpha-D-glucuronate
edaravone beta-D-glucuronate + UDP
-
Substrates: i.e. 3-methyl-1-phenyl-2-pyrazolin-5-one. Edaravone glucuronidation in liver microsomes and kidney microsomes exhibits biphasic kinetics. UDP glucuronosyltransferases UGT1A1, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10, UGT2B7, and UGT2B17 produce a significant amount of glucuronide metabolite. Among them, UGT1A9 exhibits the highest activity, followed by UGT2B17 and UGT1A7
Products: -
?
entacapone + UDP-glucuronate
UDP + entacapone-3-O-glucuronide
-
Substrates: -
Products: -
?
epirubicin + UDP-glucuronate
UDP + epirubicin beta-D-glucuronoside
epitestosterone + UDP-glucuronate
UDP + epitestosterone 17-O-glucuronide
epitestosterone + UDP-glucuronate
UDP + epitestosterone O-glucuronide
-
Substrates: glucuronidated by HGT2B7H and HGT2B7Y
Products: -
?
estradiol + UDP-alpha-D-glucuronate
UDP + estradiol 3-O-glucuronide
-
Substrates: substrate of isoform UGT1A1
Products: -
?
estradiol + UDP-glucuronate
?
Substrates: -
Products: -
?
estradiol + UDP-glucuronate
estradiol 3-O-glucuronate + UDP
Substrates: sigmoidal kinetics with n of 1.7
Products: -
?
estriol + UDP-glucuronate
?
estriol + UDPglucuronate
UDP + estriol-16 alpha-glucuronide
estrogen + UDP-glucuronate
?
estrone + UDP-glucuronate
UDP + estrone 3-O-glucuronide
Substrates: -
Products: -
?
estrone + UDPglucuronate
UDP + estrone 3-O-glucuronide
etoposide + UDP-glucuronate
?
Substrates: -
Products: -
?
etoposide + UDP-glucuronate
UDP + etoposide glucuronide
eugenol + UDP-glucuronate
?
Substrates: -
Products: -
?
eugenol + UDP-glucuronate
UDP + eugenol-O-alpha-D-glucuronide
Substrates: -
Products: -
?
flavopiridol + UDP-glucuronate
UDP + flavopiridol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, P35503, P54855, O75795, P06133, P36537, P35504 Substrates: -
Products: -
?
fluconazole + UDP-alpha-D-glucuronate
fluconazole D-glucuronate + UDP
-
Substrates: -
Products: -
?
flurbiprofen + UDP-glucuronate
?
Substrates: metabilized by mutant enzyme S432G-UGT1A7, but not by wild-type enzyme UGT1A7
Products: -
?
frusemide + UDP-alpha-D-glucuronate
frusemide D-glucuronide
-
Substrates: -
Products: -
?
glycolithocholic acid + UDPglucuronate
UDP + glycolithocholic acid O-glucuronide
-
Substrates: lowest activity among five bile acids studied
Products: -
?
glycyrrhetinic acid + UDP-glucuronate
UDP + glycyrrhetinic acid-3-O-glucuronide
-
Substrates: -
Products: -
?
hyodeoxycholic acid + UDP-glucuronate
?
hyodeoxycholic acid + UDPglucuronate
UDP + hyodeoxycholic acid O-glucuronide
-
Substrates: -
Products: -
?
ibuprofen + UDPglucuronate
UDP + ?
-
Substrates: -
Products: -
?
imipramine + UDP-glucuronate
UDP + ?
P16662, P19224, O60656, P22309, P22310, P35503, P54855, O75795, P06133, P36537, P35504 Substrates: -
Products: -
?
imipramine + UDPglucuronate
UDP + ?
-
Substrates: only UGP1AY shows activity
Products: -
?
itraconazole + UDP-alpha-D-glucuronate
?
-
Substrates: -
Products: -
?
ketoconazole + UDP-alpha-D-glucuronate
?
-
Substrates: -
Products: -
?
lamotrigine + UDP-alpha-D-glucuronate
lamotrigine D-glucuronate + UDP
-
Substrates: -
Products: -
?
lamotrigine + UDP-glucuronate
UDP + ?
-
Substrates: -
Products: -
?
lithocholic acid + UDPglucuronate
UDP + ?
lorazepam + UDP-glucuronate
?
Substrates: -
Products: -
?
miconazole + UDP-alpha-D-glucuronate
miconazole D-glucuronate + UDP
-
Substrates: -
Products: -
?
midazolam + UDP-alpha-D-glucuronate
midazolam D-glucuronide + UDP
-
Substrates: -
Products: -
?
milnacipran + UDP-glucuronate
?
Substrates: -
Products: -
?
morphine + UDP-glucuronate
UDP + morphine 3,6-diglucuronide
morphine + UDP-glucuronate
UDP + morphine 3-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, P35503, P54855, O75795, P06133, P36537, P35504 Substrates: -
Products: -
?
morphine + UDP-glucuronate
UDP + morphine 3-glucuronide + morphine 6-glucuronide
Substrates: -
Products: -
?
morphine + UDP-glucuronate
UDP + morphine-3-glucuronide
-
Substrates: -
Products: -
?
mycophenolate + UDP-glucuronate
?
Substrates: -
Products: -
?
mycophenolic acid + UDP-alpha-D-glucuronate
mycophenolic acid D-glucuronide
-
Substrates: -
Products: -
?
mycophenolic acid + UDP-glucuronate
UDP + mycophenolic acid beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, P35503, P54855, O75795, P06133, P36537, P35504 Substrates: -
Products: -
?
N-hydroxy-2-acetylaminofluorene + UDPglucuronate
UDP + N-hydroxy-2-acetylaminofluorene O-glucuronide
-
Substrates: glucuronidated by UGT1A3 in preference to the ring-hydroxylated derivatives
Products: -
?
N-hydroxy-2-naphthylamine + UDPglucuronate
UDP + N-hydroxy-2-naphthylamine-O-glucuronide
-
Substrates: -
Products: -
?
naproxen + UDP-glucuronate
naproxen glucuronide + UDP
-
Substrates: -
Products: -
?
octylgallate + UDPglucuronate
?
Substrates: -
Products: -
?
olanzapine + UDP-glucuronate
?
Substrates: -
Products: -
?
opiates + UDPglucuronate
opiates 6-O-glucuronides + UDP
-
Substrates: substrate for UGT2B7
Products: -
?
oxazepam + UDP-glucuronate
?
Substrates: -
Products: -
?
oxazepam + UDP-glucuronate
UDP + oxazepam beta-D-glucuronoside
-
Substrates: -
Products: -
?
p-cresol + UDP-glucuronate
UDP + p-cresyl beta-D-glucuronide
Substrates: among isoforms UGT1A1, 1A3, 1A4, 1A6, 1A7, 1A8, 1A9, 1A10, 2B4, 2B7, 2B10, 2B15, and 2B17 tesed, only UGT1A6 and UGT1A9 show activity with p-cresol
Products: -
?
p-ethoxyphenylurea + UDP-glucuronate
?
Substrates: -
Products: -
?
posaconazole + UDP-glucuronate
UDP + posaconazole beta-D-glucuronoside
-
Substrates: -
Products: -
?
profen + UDPglucuronate
UDP + ?
-
Substrates: glucuronidated by UGT2B7
Products: -
?
propofol + UDP-alpha-D-glucuronate
UDP + propofol D-glucuronide
propofol + UDP-glucuronate
UDP + propofol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P06133, A0A0G2JMZ5, D6RH08 Substrates: -
Products: -
?
propofol + UDP-glucuronate
UDP + propofol O-glucuronide
Substrates: -
Products: -
?
quercetin + UDP-glucuronate
UDP + quercetin 7-glucuronide + quercetin 4'-glucuronide + quercetin 3'-glucuronide
Substrates: isoform UGT1A1 mainly converts quercetin into three monoglucuronides, including 7-glucuronide, 4'-glucuronide, and 3'-glucuronide
Products: -
?
quercetin + UDPglucuronate
UDP + quercetin O-glucuronide
-
Substrates: -
Products: -
?
retigabine + UDP-alpha-D-glucuronate
retigabine D-glucuronide
-
Substrates: -
Products: -
?
retigabine + UDP-glucuronate
UDP + retigabine N-glucuronide
-
Substrates: -
Products: -
?
scopoletin + UDP-glucuronate
?
Substrates: -
Products: -
?
scopoletin + UDP-glucuronate
UDP + scopoletin O-glucuronide
scopoletin + UDPglucuronate
UDP + scopoletin O-glucuronide
senecionine + UDP-alpha-D-glucuronate
senecionine N-glucuronide + UDP
-
Substrates: senecionine is a representative of the hepatotoxic pyrrolizidine alkaloids. Glucuronidation is mediated by isofrom UGT1A4 and follows typical Michaelis-Menten kinetics
Products: -
?
serotonin + UDP-glucuronate
UDP + 3-(2-aminoethyl)-1H-indol-5-yl beta-D-glucuronide
serotonin + UDP-glucuronate
UDP + serotonin beta-D-glucuronide
serotonin + UDP-glucuronate
UDP + serotonin O-glucuronide
Substrates: -
Products: -
?
silybin A + UDP-glucuronate
UDP + ?
Substrates: -
Products: -
?
silybin B + UDP-glucuronate
UDP + ?
Substrates: -
Products: -
?
silydianin + UDP-glucuronate
UDP + silydianin beta-D-glucuronide
Substrates: -
Products: -
?
SN-38 + UDP-glucuronate
UDP + 7-ethyl-10-hydroxycamptothecin 10-O-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, P35503, P54855, O75795, P06133, P36537, P35504 Substrates: -
Products: -
?
sulconazole + UDP-alpha-D-glucuronate
sulconazole D-glucuronate + UDP
-
Substrates: -
Products: -
?
sulfinpyrazone + UDP-alpha-D-glucuronate
sulfinpyrazone D-glucuronide
-
Substrates: -
Products: -
?
tamoxifen + UDP-alpha-D-glucuronate
tamoxifen-N-glucuronate + UDP
-
Substrates: -
Products: -
?
tamoxifen + UDP-glucuronate
UDP + ?
-
Substrates: -
Products: -
?
testosterone + UDP-glucuronate
UDP + testosterone 17-O-glucuronide
-
Substrates: isoform UGT2B17 is the most active enzyme in testosterone glucuronidation. Isoform UGT2A1, an extrahepatic enzyme that is expressed mainly in the nasal epithelium, catalyzes the glucuronidation of both steroids at considerable rates and similar kinetics
Products: -
?
testosterone + UDP-glucuronate
UDP + testosterone beta-D-glucuronoside
testosterone + UDPglucuronate
UDP + testosterone O-glucuronide
-
Substrates: no activity
Products: -
?
thyroxine + UDP-glucuronate
UDP + thyroxine beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, P35503, P54855, O75795, P06133, P36537, P35504 Substrates: -
Products: -
?
tioconazole + UDP-alpha-D-glucuronate
tioconazole D-glucuronate + UDP
-
Substrates: -
Products: -
?
tranilast + UDP-glucuronate
tranilast glucuronoside + UDP
Substrates: -
Products: -
?
trans-4-hydroxytamoxifen + UDP-glucuronate
UDP + ?
-
Substrates: -
Products: -
?
trans-androsterone + UDP-alpha-D-glucuronate
trans-androsterone D-glucuronate + UDP
-
Substrates: -
Products: -
?
trans-endoxifen + UDP-glucuronate
UDP + ?
-
Substrates: -
Products: -
?
trifluoperazine + UDP-glucuronate
UDP + ?
-
Substrates: substrate for isoform UGT1A4 and isoform UGT1A1 mutant H39P
Products: -
?
trifluoperazine + UDP-glucuronate
UDP + trifluoperazine beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P06133, A0A0G2JMZ5, D6RH08 Substrates: -
Products: -
?
trifluoperazine + UDP-glucuronate
UDP + trifluoperazine N-glucuronide
Substrates: -
Products: -
?
trifluoperazine dihydrochloride + UDP-glucuronate
UDP + ?
Substrates: substrate for isoform UGT1A4
Products: -
?
troglitazone + UDPglucuronate
UDP + troglitazone 6-O-glucuronide
-
Substrates: -
Products: -
?
UDP-alpha-D-glucuronate + (R)-propranolol
UDP + (R)-propranolol beta-D-glucuronoside
UDP-alpha-D-glucuronate + (S)-naproxen
UDP + beta-D-glucuronosyl (S)-naproxen
-
Substrates: -
Products: -
?
UDP-alpha-D-glucuronate + (S)-propranolol
UDP + (S)-propranolol beta-D-glucuronoside
UDP-alpha-D-glucuronate + 3-hydroxyflavone
UDP + 3-[(beta-D-glucopyranurnosyl)oxy]-flavone
Substrates: isozyme UGT1A1
Products: -
?
UDP-alpha-D-glucuronate + 7-ethyl-10-hydroxycamptothecin
UDP + 7-ethyl-10-hydroxycampothecin 1-O-beta-D-glucuronide
Substrates: -
Products: -
?
UDP-alpha-D-glucuronate + chloramphenicol
UDP + chloramphenicol beta-D-glucuronide
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
?
UDP-alpha-D-glucuronate + diclofenac
UDP + diclofenac O-beta-D-glucuronide
Substrates: -
Products: -
?
UDP-alpha-D-glucuronate + dopamine
UDP + dopamine 3-O-beta-D-glucopyranosiduronic acid
-
Substrates: substrate for isoform UGT1A10, no substrate for all other UGT enzymes tested
Products: -
?
UDP-alpha-D-glucuronate + dopamine
UDP + dopamine 4-O-beta-D-glucopyranosiduronic acid
-
Substrates: -
Products: substrate for isoform UGT1A10, no substrate for all other UGT enzymes tested
?
UDP-alpha-D-glucuronate + sorafenib
UDP + ?
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
?
UDP-alpha-glucuronate + diclofenac
UDP + beta-D-glucuronosyl-diclofenac
-
Substrates: -
Products: -
?
UDP-D-glucuronate + 1-naphthol
UDP + 1-naphthyl beta-D-glucuronoside
UDP-D-glucuronate + 11alpha-hydroxyprogesterone
UDP + 11alpha-hydroxyprogesterone 11-O-beta-D-glucuronoside
Substrates: an UGT2B7 substrate
Products: -
?
UDP-D-glucuronate + 17beta-estradiol
UDP + 17beta-estradiol 3-O-beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + 17beta-estradiol
UDP + 17beta-estradiol-3-O-beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + 1alpha,25-dihydroxyvitamin D3
UDP + 1alpha,25-dihydroxyvitamin D3 25-O-beta-D-glucuronoside
Substrates: among 12 different UGT isozymes tested, only UGT1A4, and also UGT2B4 and UGT2B7 support the reaction, the main product by UGT1A4 supersomes and human liver microsomes is the 25-O-glucuronide, product identification and determination by mass spectral and NMR analyses, overview
Products: -
?
UDP-D-glucuronate + 2-hydroxyestradiol
UDP + 2-hydroxyestradiol beta-D-glucuronoside
Substrates: isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + 2-hydroxyestrone
UDP + 2-hydroxyestrone beta-D-glucuronoside
Substrates: isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + 2-naphthol
UDP + 2-naphthyl beta-D-glucuronoside
UDP-D-glucuronate + 3'-azido-3'-deoxythymidine
UDP + 3'-azido-3'-deoxythymidine 5'-O-beta-D-glucuronoside
Substrates: model substrate for determination of glucuronidation with respect to specificity, linearity, detection limit, recovery, stability, precision and accuracy, method development and validation for assay and chromatographic determination of reaction products, overview
Products: -
?
UDP-D-glucuronate + 3-hydroxydesloratadine
UDP + 3-hydroxydesloratadine beta-O-D-glucuronoside
Substrates: specific substrate of isozyme UGT1A8
Products: -
?
UDP-D-glucuronate + 4'-hydroxy-warfarin
UDP + 4'-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A10
Products: -
?
UDP-D-glucuronate + 4-(trifluoromethyl)-umbelliferone
UDP + 4-(trifluoromethyl)-umbelliferone beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + 4-hydroxy-estrone
UDP + ?
Substrates: -
Products: -
?
UDP-D-glucuronate + 4-hydroxy-N-desmethyl-tamoxifen
UDP + 4-hydroxy-N-desmethyl-tamoxifen beta-D-glucuronoside
UDP-D-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferone beta-D-glucuronoside
UDP-D-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferonyl beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferyl beta-D-glucuronoside
UDP-D-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferyl beta-O-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + 4-nitrophenol
UDP + 4-nitrophenyl beta-D-glucuronoside
UDP-D-glucuronate + 4-nitrophenol
UDP + 4-nitrophenyl beta-O-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + 5alpha-androstane-3alpha,17beta-diol
UDP + ?
-
Substrates: -
Products: -
?
UDP-D-glucuronate + 6-hydroxy-warfarin
UDP + 6-hydroxy-warfarin beta-D-glucuronoside
UDP-D-glucuronate + 7-hydroxy-warfarin
UDP + 7-hydroxy-warfarin beta-D-glucuronoside
UDP-D-glucuronate + 8-hydroxy-warfarin
UDP + 8-hydroxy-warfarin beta-D-glucuronoside
UDP-D-glucuronate + acacetin
UDP + acacetin 7-O-beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
UDP-D-glucuronate + androstane-3alpha,17beta-diol
UDP + ?
UDP-D-glucuronate + androsterone
UDP + androsterone 3-O-beta-D-glucuronoside
UDP-D-glucuronate + anthraflavic acid
UDP + ?
-
Substrates: -
Products: -
?
UDP-D-glucuronate + apigenin
UDP + apigenin 7-O-beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + beta-D-estradiol
UDP + beta-estradiol 3-O-beta-D-glucuronoside
Substrates: isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + beta-estradiol
UDP + beta-estradiol 3-O-beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + bilirubin
UDP + ?
-
Substrates: -
Products: -
?
UDP-D-glucuronate + bilirubin
UDP + bilirubin beta-D-glucuronoside
Substrates: isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + bisdemethoxy-curcumin
UDP + bisdemethoxy-curcumin phenolic beta-D-monoglucuronide
-
Substrates: -
Products: -
?
UDP-D-glucuronate + candesartan
UDP + candesartan beta-D-glucuronoside
-
Substrates: isozyme UGT1A3 exhibites a strong regioselectivity towards the N2 position of the tetrazole ring, also isozyme UGT2B7 glucuronidates candesartan at the tetrazole-N2 position, whereas isozymes UGT1A7, UGT1A8, UGT1A9, and UGT1A10 mainly yield candesartan O-glucuronide
Products: -
?
UDP-D-glucuronate + capsaicin
UDP + capsaicin beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + chenodeoxycholic acid
UDP + hyodeoxycholic acid 6-O-glucuronoside
Substrates: isozyme UGT2A3
Products: -
?
UDP-D-glucuronate + cis-4-hydroxytamoxifen
UDP + 4-hydroxytamoxifen beta-D-glucuronoside
UDP-D-glucuronate + cotinine
UDP + ?
UDP-D-glucuronate + curcumin
UDP + curcumin beta-D-glucuronoside
UDP-D-glucuronate + curcumin
UDP + curcumin phenolic beta-D-monoglucuronide
UDP-D-glucuronate + dehydrotestosterone
UDP + dehydrotestosterone 17-O-beta-D-glucuronoside
UDP-D-glucuronate + demethoxy-curcumin
UDP + demethoxy-curcumin phenolic beta-D-monoglucuronide
-
Substrates: -
Products: -
?
UDP-D-glucuronate + deoxycholic acid
UDP + hyodeoxycholic acid 6-O-glucuronoside
Substrates: isozyme UGT2A3
Products: -
?
UDP-D-glucuronate + dihydrotestosterone
UDP + dihydrotestosterone 17-O-beta-D-glucuronoside
UDP-D-glucuronate + eriodictyol
UDP + eriodictyol 7-O-beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + estradiol
UDP + estradiol 3-O-beta-D-glucuronoside
UDP-D-glucuronate + estradiol
UDP + estradiol-3-beta-D-glucuronoside
UDP-D-glucuronate + estriol
UDP + ?
-
Substrates: -
Products: -
?
UDP-D-glucuronate + estriol
UDP + estriol 3-O-beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + estriol
UDP + estriol glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + eugenol
UDP + eugenol beta-D-glucuronoside
UDP-D-glucuronate + flurbiprofen
UDP + flurbiprofen beta-D-glucuronoside
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Substrates: isozyme UGT2B7
Products: -
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UDP-D-glucuronate + frusemide
UDP + frusemide beta-D-glucuronoside
UDP-D-glucuronate + gemfibrozil
UDP + gemfibrozil beta-D-glucuronoside
UDP-D-glucuronate + hesperetin
UDP + hesperetin 7-O-beta-D-glucuronoside
-
Substrates: -
Products: -
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UDP-D-glucuronate + homoeriodictyol
UDP + homoeriodictyol 7-O-beta-D-glucuronoside
-
Substrates: -
Products: -
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UDP-D-glucuronate + hyodeoxycholic acid
UDP + hyodeoxycholic acid 24-carboxy-glucuronoside
Substrates: recombinant enzyme, expressed in insect cells via baculovirus system, selective glucuronidation
Products: product formation depends on the isozyme, overview
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UDP-D-glucuronate + hyodeoxycholic acid
UDP + hyodeoxycholic acid 3-O-glucuronoside
Substrates: recombinant enzyme, expressed in insect cells via baculovirus system, selective glucuronidation
Products: product formation depends on the isozyme, overview
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UDP-D-glucuronate + hyodeoxycholic acid
UDP + hyodeoxycholic acid 6-O-glucuronoside
UDP-D-glucuronate + imipramine
UDP + imipramine N-beta-D-glucuronoside
Substrates: reaction of isozyme UGT1A4
Products: -
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UDP-D-glucuronate + isolongifolol
UDP + isolongifolol beta-D-glucuronoside
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Substrates: the compound is substrate and competitive inhibitor
Products: -
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UDP-D-glucuronate + kaempferol
UDP + kaempferol 7-O-beta-D-glucuronoside
-
Substrates: -
Products: -
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UDP-D-glucuronate + labetalol
UDP + ?
UDP-D-glucuronate + longifolol
UDP + longifolol beta-D-glucuronoside
-
Substrates: the compound is substrate and competitive inhibitor
Products: -
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UDP-D-glucuronate + losartan
UDP + losartan beta-D-glucuronoside
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Substrates: no O-glucuronide is generated by any isozyme, while isozymes UGT1A1, UGT1A3, 1A10, UGT2B7, and UGT2B17 glucuronidate losartan at the tetrazole-N2, isozyme UGT1A10 also yields the respective N1-glucuronide, isozyme UGT1A3 exhibites a strong regioselectivity towards the N2 position of the tetrazole ring
Products: -
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UDP-D-glucuronate + luteolin
UDP + luteolin 7-O-beta-D-glucuronoside
-
Substrates: -
Products: -
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UDP-D-glucuronate + menadiol
UDP + mendadiol 1-O-beta-D-glucuronoside
UDP-D-glucuronate + menadiol
UDP + mendadiol 4-O-beta-D-glucuronoside
UDP-D-glucuronate + morphine
UDP + morphine 3-beta-D-glucuronoside
Substrates: activity of isozyme UGT1A8
Products: -
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UDP-D-glucuronate + morphine
UDP + morphine 3-O-beta-D-glucuronoside
UDP-D-glucuronate + morphine
UDP + morphine 6-beta-D-glucuronoside
UDP-D-glucuronate + mycophenolic acid
UDP + mycophenolic acid beta-D-glucuronoside
Substrates: K314 and K404m are determined binding sites required for UDP-glcA binding to isozyme UGT1A10, overview
Products: -
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UDP-D-glucuronate + myricetin
UDP + myricetin 7-O-beta-D-glucuronoside
-
Substrates: -
Products: -
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UDP-D-glucuronate + naringenin
UDP + naringenin 7-O-beta-D-glucuronoside
-
Substrates: -
Products: -
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UDP-D-glucuronate + nicotine
UDP + ?
UDP-D-glucuronate + octylgallate
UDP + octylgallate beta-D-glucuronoside
UDP-D-glucuronate + phenolphthalein
UDP + phenolphthalein beta-D-glucuronoside
Substrates: an UGT2B15 substrate
Products: -
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UDP-D-glucuronate + phenolphthalein
UDP + phenolphthalein beta-D-monoglucuronoside
-
Substrates: -
Products: -
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UDP-D-glucuronate + phloretin
UDP + ?
-
Substrates: -
Products: -
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UDP-D-glucuronate + propofol
UDP + propofol beta-D-glucuronoside
UDP-D-glucuronate + protocatechuic aldehyde
UDP + ?
UDP-D-glucuronate + quercetin
UDP + quercetin 7-O-beta-D-glucuronoside
-
Substrates: -
Products: -
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UDP-D-glucuronate + rasloxifene
UDP + raloxifene-6-beta-glucuronide
Substrates: -
Products: -
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UDP-D-glucuronate + scopoletin
UDP + scopoletin beta-D-glucuronoside
UDP-D-glucuronate + serotonin
UDP + serotonin beta-D-glucuronoside
Substrates: isozyme UGT1A6
Products: -
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UDP-D-glucuronate + serotonin
UDP + serotonin O-beta-D-glucuronoside
Substrates: reaction of isozyme UGT1A6
Products: -
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UDP-D-glucuronate + tamoxifen + H+
UDP + tamoxifen beta-D-glucuronoside
UDP-D-glucuronate + testosterone
UDP + testosterone 17-O-beta-D-glucuronoside
Substrates: an UGT2B15 substrate
Products: -
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UDP-D-glucuronate + tetrahydrocurcumin
UDP + tetrahydrocurcumin beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + thyroxine
UDP + thyroxine beta-D-glucuronoside
UDP-D-glucuronate + tizoxanide
UDP + tizoxanide beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + trans-4-hydroxytamoxifen
UDP + 4-hydroxytamoxifen beta-D-glucuronoside
UDP-D-glucuronate + trifluoperazine
UDP + trifluoperazine beta-D-glucuronoside
-
Substrates: -
Products: -
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UDP-D-glucuronate + umbelliferone
UDP + umbelliferyl beta-D-glucuronoside
-
Substrates: -
Products: -
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UDP-D-glucuronate + ursodeoxycholic acid
UDP + hyodeoxycholic acid 6-O-glucuronoside
Substrates: isozyme UGT2A3
Products: -
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UDP-D-glucuronate + zidovudine
UDP + zidovudine beta-D-glucuronoside
UDP-D-glucuronate + zolarsartan
UDP + zolarsartan beta-D-glucuronoside
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Substrates: isozyme UGT1A3 exhibites a strong regioselectivity towards the N2 position of the tetrazole ring, the tetrazole-N1 of this aglycone is accessible to other enzymes, including isozyme UGT1A5, zolarsartan O-glucuronide is mainly produced by isozyme UGT1A10 and isozyme UGT2B7
Products: -
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UDP-glucuronate + (E)-2,4-dimethoxy-6-(4-methoxystyryl)benzaldehyde oxime
UDP + 1-O-[(E)-2,4-dimethoxy-6-(4-methoxystyryl)benzaldehyde oxime]-beta-D-glucuronate
UDP-glucuronate + (E)-3-(3-hydroxy-4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)acrylic acid
UDP + ?
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Substrates: i.e. NI-12a, low activity, NI-12a is glucuronidated at both the -COOH and -OH functions. NI-12a is primarily metabolized by the hepatic and renal enzyme UGT1A9
Products: -
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UDP-glucuronate + (S)-oxazepam
UDP + (S)-oxazepam beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + 1,25-dihydroxyergocalciferol
UDP + 1,25-dihydroxyergocalciferol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + 1-hydroxypyrene
UDP + 1-hydroxypyrene beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + 1-naphthol
UDP + 1-naphthol beta-D-glucuronide
UDP-glucuronate + 1-naphthol
UDP + beta-D-glucuronosyl-(1-naphthol)
-
Substrates: -
Products: -
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UDP-glucuronate + 10-gingerol
UDP + 10-gingerol 4'-O-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
Products: -
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UDP-glucuronate + 10-gingerol
UDP + 10-gingerol 5-O-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
Products: -
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UDP-glucuronate + 12-hydroxyeicosatetraenoic acid
UDP + 12-hydroxyeicosatetraenoyl beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + 12-hydroxyeicosatetraenoic acid
UDP + 12-hydroxyeicosatetraenoyl-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + 15-hydroxyeicosatetraenoic acid
UDP + 15-hydroxyeicosatetraenoyl beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + 15-hydroxyeicosatetraenoic acid
UDP + 15-hydroxyeicosatetraenoyl-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + 17-alpha-estradiol
UDP + 17-alpha-estradiol 3-O-beta-D-glucuronoside
UDP-glucuronate + 17-beta-estradiol
UDP + 17-beta-estradiol 3-beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + 17-beta-estradiol
UDP + 17-beta-estradiol 3-O-beta-D-glucuronoside
UDP-glucuronate + 17beta-estradiol
UDP + 17beta-estradiol 3-O-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + 17beta-estriol
UDP + estriol 17-beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + 2',4'-dihydroxychalcone
UDP + 2'-hydroxychalcone 4'-O-beta-D-glucuronoside
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Substrates: glucuronidation at the OH-4' position by UGT1A1 and UGT1A10 isoforms, both UGT1A6 and 1A9 produced two chalcone monoglucuronides, the 4'-Oglucuronide and the 2'-O-glucuronide
Products: -
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UDP-glucuronate + 2',4'-dihydroxychalcone
UDP + 4'-hydroxychalcone 2'-O-beta-D-glucuronoside
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Substrates: glucuronidation at the OH-2' position with low activity by UGT1A7, UGT1A6, and UGT1A10 isoforms, and with high activity by isozyme UGT1A9. Both UGT1A6 and 1A9 produced two chalcone monoglucuronides, the 4'-Oglucuronide and the 2'-O-glucuronide
Products: -
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UDP-glucuronate + 2',4,4',6'-tetrahydroxychalcone
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UDP-glucuronate + 2'-hydroxychalcone
UDP + chalcone 2'-O-beta-D-glucuronoside
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Substrates: glucuronidation at the OH-2' position by UGT1A9 isoform
Products: -
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UDP-glucuronate + 2-hydroxyestrone
UDP + 2-hydroxyestrone beta-D-glucuronide
-
Substrates: -
Products: -
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UDP-glucuronate + 2-methoxyestrone
UDP + 2-methoxyestrone beta-D-glucuronide
-
Substrates: -
Products: -
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UDP-glucuronate + 20-hydroxyeicosatetraenoic acid
UDP + 20-hydroxyeicosatetraenoyl beta-D-glucuronoside
UDP-glucuronate + 25-hydroxyergocalciferol
UDP + 25-hydroxyergocalciferol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + 3'-azido-3'-deoxythymidine
UDP + 3'-azido-3'-deoxythymidine beta-D-glucuronide
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Substrates: isozymes UGT2B4, UGT2B7, and UGT2B17
Products: -
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UDP-glucuronate + 3'-azido-3'-deoxythymidine
UDP + 3'-azido-3'-deoxythymidine beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + 3,17-estradiol
UDP + 17-estradiol 3-O-glucuronide
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Substrates: isozyme UGT1A1
Products: -
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UDP-glucuronate + 3,17-estradiol
UDP + 3-estradiol 17-O-glucuronide
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Substrates: isozyme UGT1A1
Products: -
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UDP-glucuronate + 3,2'-dihydroxychalcone
UDP + 3-hydroxychalcone 2'-O-beta-D-glucuronoside
UDP-glucuronate + 3-epideacetycinobufagin
UDP + 3-epideacetycinobufagin 3-beta-D-glucuronoside
UDP-glucuronate + 3alpha,5beta-tetrahydroaldosterone
UDP + 3alpha,5beta-tetrahydroaldosterone beta-D-glucuronide
Substrates: high activity
Products: -
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UDP-glucuronate + 4,2'-dihydroxychalcone
UDP + 4-hydroxychalcone 2'-O-beta-D-glucuronoside
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Substrates: glucuronidation at the OH-2' position by UGT1A8, UGT1A1, and UGT1A3 isoforms. The A-ring OH-4 group promotes glucuronidation at the 2' position for the reaction of the exclusive substrate 4,2'-dihydroxychalcone of UGT1A1 and 1A3
Products: -
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UDP-glucuronate + 4-aminobiphenyl
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Substrates: -
Products: -
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UDP-glucuronate + 4-ethylphenol
UDP + beta-D-glucuronosyl-(4-ethylphenol)
-
Substrates: -
Products: -
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UDP-glucuronate + 4-hydroxy-estrone
UDP + ?
Substrates: glucuronidation of 4-hydroxylated estrone is significantly reduced in breast carcinomas compared to healthy
Products: -
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UDP-glucuronate + 4-hydroxyestradiol
UDP + 4-hydroxyestradiol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
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UDP-glucuronate + 4-hydroxyretinoic acid
UDP + 4-hydroxyretinoic acid beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: mainly conjugated by UGT2B7
Products: -
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UDP-glucuronate + 4-methoxyestrone
UDP + 4-methoxyestrone beta-D-glucuronide
-
Substrates: -
Products: -
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UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferone beta-D-glucuronide
UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferyl beta-D-glucuronoside
UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferyl-beta-D-glucuronide
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Substrates: all isozymes, nonselective substrate
Products: -
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UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferyl-beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + 4-methylumbelliferone
UDP + beta-D-glucuronosyl-(4-methylumbelliferone)
-
Substrates: -
Products: -
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UDP-glucuronate + 4-nitrophenol
UDP + 4-nitrophenol beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + 4-nitrophenol
UDP + 4-nitrophenyl beta-D-glucuronide
Substrates: recombinant isozyme UGT1A6 from lymphoblasts or insect cells
Products: -
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UDP-glucuronate + 4-nitrophenol
UDP + beta-D-glucuronosyl-(4-nitrophenol)
-
Substrates: -
Products: -
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UDP-glucuronate + 5-hydroxytryptophol
UDP + 5-hydroxy-tryptophol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
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UDP-glucuronate + 5-hydroxytryptophol
UDP + 5-hydroxytryptophol beta-D-glucuronide
Substrates: isozymes UGT1A6 and UGT1A9, the latter shows over 20fold lower activity
Products: -
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UDP-glucuronate + 5-hydroxytryptophol
UDP + 5-hydroxytryptophol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: mucosal serotonin and its metabolite 5-hydroxytryptophol are solely conjugated by UGT1A6
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UDP-glucuronate + 5alpha-dihydroaldosterone
UDP + 5alpha-dihydroaldosterone beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + 5alpha-tetrahydrocortisone
UDP + 5alpha-tetrahydrocortisone beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + 5beta-tetrahydrocortisone
UDP + 5beta-tetrahydrocortisone beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + 6-gingerol
UDP + 6-gingerol 4'-O-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
Products: -
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UDP-glucuronate + 6-gingerol
UDP + 6-gingerol 5-O-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
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UDP-glucuronate + 6-hydroxymelatonin
UDP + 6-hydroxymelatonin beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + 7-ethyl-10-hydroxy-camptothecin
UDP + 7-ethyl-10-hydroxy-camptothecin beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: i.e. SN-38, an active metabolite of irinotecan
Products: -
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UDP-glucuronate + 7-ethyl-10-hydroxycampothecin
UDP + 7-ethyl-10-hydroxycampothecin 1-O-beta-D-glucuronide
Substrates: i.e. SN-38, isozymes UGT1A1, UGT1A7, and UGT1A9
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UDP-glucuronate + 7-ethyl-10-hydroxycamptothecin
UDP + 7-ethyl-10-hydroxycamptothecin 10-O-beta-D-glucuronoside
Substrates: i.e. SN-38, an active metabolite of irinotecan
Products: -
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UDP-glucuronate + 7-hydroxy-4-trifluoromethylcoumarin
UDP + 4-trifluoromethylcoumarin 7-O-beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + 7-hydroxy-4-trifluoromethylcoumarin
UDP + 7-hydroxy-4-trifluoromethylcoumarin beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + 7-hydroxyflavanone
UDP + flavanone 7-O-beta-D-glucuronoside
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Substrates: -
Products: -
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UDP-glucuronate + 8-gingerol
UDP + 8-gingerol 4'-O-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
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UDP-glucuronate + 8-gingerol
UDP + 8-gingerol 5-O-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
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UDP-glucuronate + 8-hydroxyquinoline
UDP + 8-hydroxyquinoline beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
UDP-glucuronate + acceptor
UDP + acceptor beta-glucuronoside
UDP-glucuronate + aldosterone
UDP + aldosterone beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + all-trans-retinoic acid
UDP + all-trans-retinoic acid beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: mainly conjugated by UGT2B7
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UDP-glucuronate + Aloe-emodin
UDP + Aloe-emodin beta-D-glucuronide
Substrates: isozyme UGT1A7
Products: -
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UDP-glucuronate + alpinetin
UDP + alpinetin beta-D-glucuronoside
-
Substrates: -
Products: -
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UDP-glucuronate + amitriptyline
UDP + amitriptyline beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + amitryptiline
UDP + amitryptiline beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
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UDP-glucuronate + androstane-3,17-diol
UDP + androstane-3,17-diol 17-O-beta-D-glucuronide
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Substrates: isozyme UGT2B15
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UDP-glucuronate + androstane-3,17-diol
UDP + beta-D-glucuronosyl-androstane-3,17-diol
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Substrates: -
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UDP-glucuronate + androstanediol
UDP + androstanediol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + anthraflavic acid
UDP + anthraflavic acid 2-glucuronide
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Substrates: isozyme UGT1A1
Products: -
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UDP-glucuronate + anthraflavic acid
UDP + anthraflavic acid 2-O-beta-D-glucuronide
UDP-glucuronate + apigenin
UDP + apigenin beta-D-glucuronide
UDP-glucuronate + asialo-orosomucoid
UDP + asialo-orosomucoid beta-D-glucuronide
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Substrates: acceptor is a glycoprotein, preferred substrate
Products: -
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UDP-glucuronate + beta-estradiol
UDP + estradiol 3-beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + bilirubin
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Substrates: -
Products: -
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UDP-glucuronate + bilirubin
UDP + bilirubin beta-D-glucuronoside
UDP-glucuronate + biochanin A
UDP + biochanin A beta-D-glucuronide
UDP-glucuronate + buprenorphine
UDP + buprenorphine glucuronide
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Substrates: isozyme UGT1A1
Products: -
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UDP-glucuronate + capsaicin
UDP + capsaicin beta-D-glucuronide
UDP-glucuronate + cardamonin
UDP + cardamonin beta-D-glucuronoside
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Substrates: UGT1A9 is the only isoform to glucuronidate cardamonin at the OH-2' position, lower activity with isozyme UGT1A7
Products: -
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UDP-glucuronate + carvedilol
UDP + carvedilol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + chenodeoxycholic acid
UDP + chenodeoxycholic acid 24-beta-D-glucuronoside
UDP-glucuronate + cholic acid
UDP + cholic acid 24-beta-D-glucuronoside
UDP-glucuronate + chrysin
UDP + chrysin beta-D-glucuronide
UDP-glucuronate + citronellol
UDP + citronellol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + clozapine
UDP + clozapine beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + codeine
UDP + beta-D-glucuronosyl-codeine
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Substrates: low activity
Products: -
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UDP-glucuronate + codeine
UDP + codeine beta-D-glucuronide
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Substrates: isozymes UGT2B4 and UGT2B7
Products: -
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UDP-glucuronate + cotinine
UDP + cotinine N-beta-D-glucuronoside
Substrates: cotinine is a highly selective substrate of human liver microsomal UGT2B10
Products: -
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UDP-glucuronate + curcumin
UDP + curcumin beta-D-glucuronide
UDP-glucuronate + cyproheptadine
UDP + cyproheptadine beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + deferiprone
UDP + deferiprone beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + denopamine
UDP + denopamine beta-D-glucuronide
Substrates: -
Products: formation of 1 product metabolite termed G2
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UDP-glucuronate + deoxycholic acid
UDP + deoxycholic acid 24-beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + desmethylnaproxen
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UDP-glucuronate + diclofenac
UDP + diclofenac beta-D-glucuronoside
UDP-glucuronate + dihydrotestosterone
UDP + dihydrotestosterone beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + diphenhydramine
UDP + diphenhydramine beta-D-glucuronoside
UDP-glucuronate + dopamine
UDP + dopamine beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + entacapone
UDP + entacapone beta-D-glucuronide
UDP-glucuronate + entacapone
UDP + entacapone beta-D-glucuronoside
UDP-glucuronate + epirubicin
UDP + epirubicin beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + epitestosterone
UDP + epitestosterone beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + estradiol
UDP + estradiol beta-D-glucuronide
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Substrates: -
Products: -
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UDP-glucuronate + estradiol
UDP + estradiol beta-D-glucuronoside
UDP-glucuronate + estriol
UDP + estriol beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + estrone
UDP + estrone beta-D-glucuronide
-
Substrates: -
Products: -
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UDP-glucuronate + estrone
UDP + estrone beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + ethanol
UDP + ethyl beta-D-glucuronoside
UDP-glucuronate + ethinylestradiol
UDP + ethinylestradiol beta-D-glucuronoside
UDP-glucuronate + ethinylestradiol
UDP + ethinylestradiol glucuronide
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Substrates: isozyme UGT1A1
Products: -
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UDP-glucuronate + etoposide
UDP + etoposide beta-D-glucuronide
Substrates: isozyme UGT1A1 is specific for etoposide
Products: -
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UDP-glucuronate + etoposide
UDP + etoposide beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + eugenol
UDP + beta-D-glucuronosyl-eugenol
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Substrates: high activity
Products: -
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UDP-glucuronate + eugenol
UDP + eugenol beta-D-glucuronide
UDP-glucuronate + flavopiridol
UDP + flavopiridol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + flufenamic acid
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Substrates: -
Products: -
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UDP-glucuronate + gemfibrozil
UDP + beta-D-glucuronosyl-gemfibrozil
-
Substrates: -
Products: -
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UDP-glucuronate + genistein
UDP + genistein beta-D-glucuronide
UDP-glucuronate + genistein
UDP + genistein beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + gingerol
UDP + gingerol 4'-O-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
Products: -
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UDP-glucuronate + grepafloxacin
UDP + grepafloxacin beta-D-glucuronide
UDP-glucuronate + hydromorphone
UDP + beta-D-glucuronosyl-hydromorphone
-
Substrates: -
Products: -
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UDP-glucuronate + hyocholic acid
UDP + hyocholic acid 24-beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + hyodeoxycholic acid
UDP + beta-D-glucuronosyl-hyodeoxycholic acid
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Substrates: high activity
Products: -
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UDP-glucuronate + hyodeoxycholic acid
UDP + hyodeoxycholic acid 24G-beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + hyodeoxycholic acid
UDP + hyodeoxycholoyl beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + ibuprofen
UDP + beta-D-glucuronosyl-ibuprofen
-
Substrates: -
Products: -
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UDP-glucuronate + imipramine
UDP + imipramine beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + imipramine
UDP + imipramine beta-D-glucuronoside
UDP-glucuronate + imipramine
UDP + imipramine N-beta-D-glucuronoside
Substrates: specific substrate of UGT1A4
Products: -
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UDP-glucuronate + indomethacin
UDP + indomethacin beta-D-glucuronoside
UDP-glucuronate + ketoconazole
UDP + ketoconazole beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + ketoprofen
UDP + beta-D-glucuronosyl-ketoprofen
-
Substrates: -
Products: -
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UDP-glucuronate + ketotifen
UDP + ketotifen beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + ketotifen
UDP + ketotifenbeta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + L-thyroxine
UDP + L-thyroxyl beta-D-glucuronoside
UDP-glucuronate + lamotrigine
UDP + lamotrigine beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + leukotriene B4
UDP + leukotriene B4 beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + levofloxacin
UDP + levofloxacin beta-D-glucuronide
UDP-glucuronate + levomedetomidine
UDP + levomedetomidine beta-D-glucuronoside
UDP-glucuronate + lithocholic acid
UDP + lithocholic acid 3-beta-D-glucuronoside + lithocholic acid 24-beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + lorazepam
UDP + beta-D-glucuronosyl-lorazepam
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Substrates: -
Products: -
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UDP-glucuronate + lorazepam
UDP + lorazepam beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + mefenamic acid
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Substrates: -
Products: -
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UDP-glucuronate + midazolam
UDP + midazolam beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + morphine
UDP + morphine 3-beta-D-glucuronoside
UDP-glucuronate + morphine
UDP + morphine-3-beta-D-glucuronide
UDP-glucuronate + morphine
UDP + morphine-6-beta-D-glucuronide
UDP-glucuronate + morphine 3-glucuronide
UDP + ?
Substrates: -
Products: -
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UDP-glucuronate + morphine 3-glucuronide
UDP + morphine 3,6-diglucuronide
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Substrates: -
Products: -
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UDP-glucuronate + moxifloxacin
UDP + moxifloxacin beta-D-glucuronide
UDP-glucuronate + mycophenolic acid
UDP + mycophenolic acid beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + mycophenolic acid
UDP + mycophenolic acid-acyl-glucuronide
UDP-glucuronate + mycophenolic acid
UDP + mycophenolic acid-phenyl-glucuronide
UDP-glucuronate + mycophenolic acid
UDP + mycophenoloyl beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + N-acetylserotonin
UDP + N-acetylserotonin beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + naphthol
UDP + naphthol glucuronide
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Substrates: isozyme UGT1A6
Products: -
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UDP-glucuronate + naproxen
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UDP-glucuronate + naproxen
UDP + naproxen beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + naringenin
UDP + naringenin beta-D-glucuronide
UDP-glucuronate + niflumic acid
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Substrates: -
Products: -
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UDP-glucuronate + olanzapine
UDP + olanzapine beta-D-glucuronoside
UDP-glucuronate + paracetamol
UDP + paracetamol beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + paracetamol
UDP + paracetamol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + paragloboside
UDP + paragloboside beta-D-glucuronide
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Substrates: acceptor is a glycolipid, activity requires phosphatidylinositol
Products: -
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UDP-glucuronate + phenylbutazone
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Substrates: among 16 UDP-glucuronosyltransferase isoforms investigated, only UGT1A9 catalyzes PB C-glucuronidation
Products: -
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UDP-glucuronate + phloretin
UDP + phloretin beta-D-glucuronide
UDP-glucuronate + pizotifen
UDP + pizotifen beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + pregnan-3,17-diol
UDP + pregnan-3,17-diol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + propofol
UDP + propofol beta-D-glucuronide
UDP-glucuronate + propofol
UDP + propofol beta-D-glucuronoside
UDP-glucuronate + quercetin
UDP + quercetin beta-D-glucuronide
UDP-glucuronate + quercetin
UDP + quercetin beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + quinazarin
UDP + quinazarin beta-D-glucuronide
UDP-glucuronate + quinizarin
UDP + quinizarin beta-D-glucuronide
Substrates: isozyme UGT1A7
Products: -
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UDP-glucuronate + scopoletin
UDP + scopoletin beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + serotonin
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Substrates: -
Products: -
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UDP-glucuronate + serotonin
UDP + serotonin beta-D-glucuronide
UDP-glucuronate + serotonin
UDP + serotonin beta-D-glucuronoside
UDP-glucuronate + serotonin
UDP + serotonin beta-glucuronoside
Substrates: isozyme UGT2B7
Products: -
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UDP-glucuronate + sitafloxacin
UDP + sitafloxacin beta-D-glucuronide
UDP-glucuronate + tacrolimus
UDP + tacrolimus beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + tamoxifen
UDP + tamoxifen beta-D-glucuronoside
UDP-glucuronate + tamoxifen
UDP + tamoxifen N-beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + Telmisartan
UDP + Telmisartan beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + testosterone
UDP + testosterone beta-D-glucuronoside
UDP-glucuronate + thymol
UDP + thymol beta-D-glucuronide
UDP-glucuronate + thymol
UDP + thymol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + tigogenin
UDP + tigogenin beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + tolcapone
UDP + tolcapone beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + trans-androsterone
UDP + trans-androsterone beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + trans-resveratrol
UDP + trans-resveratrol beta-D-glucuronoside
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Substrates: -
Products: -
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UDP-glucuronate + trifluoperazine
UDP + trifluoperazine beta-D-glucuronide
Substrates: isozyme UGT1A4
Products: -
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UDP-glucuronate + trifluoroperazine
UDP + trifluoroperazine beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + trifluperazine
UDP + trifluperazine
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + umbelliferone
UDP + umbelliferone beta-D-glucuronide
UDP-glucuronate + valproic acid
UDP + beta-D-glucuronosyl-valproic acid
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Substrates: -
Products: -
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UDP-glucuronate + vorinostat
UDP + vorinostat beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + zidovudine
UDP + zidovudine beta-D-glucuronoside
UDP-glucuronate + zidovudine
UDP + zidovudine O-beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronic acid + 7-hydroxy-4-(trifluoromethyl)-coumarin
UDP + 7-hydroxy-4-(trifluoromethyl)-coumarin O-glucuronide
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Substrates: UGT1A6, UGT1A9, and UGT2B7
Products: -
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UDP-glucuronic acid + beta-estradiol
UDP + beta-estradiol 3-O-beta-D-glucuronide
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Substrates: UGT1A3
Products: -
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UDP-glucuronic acid + bilirubin
UDP + bilirubin-glucuronoside
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Substrates: UGT1A1
Products: -
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UDP-glucuronic acid + diclofenac
UDP + diclofenac O-glucuronide
Substrates: -
Products: -
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UDP-glucuronic acid + imipramine
UDP + imipramine N-glucuronide
Substrates: -
Products: -
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UDP-glucuronic acid + serotonin
UDP + serotonin O-glucuronide
Substrates: -
Products: -
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UDP-glucuronic acid + trifluoperazine
UDP + ?
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Substrates: UGT1A4
Products: -
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UDP-glucuronic acid + trifluoperazine
UDP + trifluoperazine N-glucuronide
Substrates: -
Products: -
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UDP-glucuronose + 2,3,4,5-tetrachlorophenol
UDP + ?
Substrates: -
Products: -
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UDP-glucuronose + 2,3,4-trichlorophenol
UDP + ?
Substrates: -
Products: -
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UDP-glucuronose + 2,4,5-trichlorophenol
UDP + ?
Substrates: -
Products: -
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UDP-glucuronose + 2,4,6-trichlorophenol
UDP + ?
Substrates: -
Products: -
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UDP-glucuronose + 2,4-dichlorophenol
UDP + ?
Substrates: -
Products: -
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UDP-glucuronose + 2-chlorophenol
UDP + 2-chlorophenyl beta-D-O-glucuronide
Substrates: -
Products: -
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UDP-glucuronose + 3,4,5-trichlorophenol
UDP + ?
Substrates: -
Products: -
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UDP-glucuronose + 3-chlorophenol
UDP + 3-chlorophenyl beta-D-O-glucuronide
Substrates: -
Products: -
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UDP-glucuronose + 4-chlorophenol
UDP + 4-chlorophenyl beta-D-O-glucuronide
Substrates: -
Products: -
?
UDP-glucuronose + chlorophenol
UDP + chlorophenyl beta-D-glucuronide
Substrates: -
Products: -
?
UDP-glucuronose + chlorophenol
UDP + chlorophenyl beta-D-glucuronoide
Substrates: -
Products: -
?
UDP-glucuronose + chlorophenol
UDP + chlorophenyl beta-D-O-glucuronide
Substrates: -
Products: -
?
UDP-glucuronose + pentachlorophenol
UDP + ?
Substrates: -
Products: -
?
UDP-glucuronose + pentachlorophenol
UDP + pentachlorophenyl beta-D-O-glucuronide
Substrates: -
Products: -
?
UDPglucuronate + naproxen
?
Substrates: UGT2B7 is responsible for human hepatic naproxen acyl glucuronidation, which is the primary elimination pathway for this drug
Products: -
?
ursodeoxycholic acid + UDPglucuronate
UDP + ursodeoxycholic acid O-glucuronide
valproic acid + UDPglucuronate
UDP + ?
vanillin + UDP-glucuronate
UDP + vanillin O-glucuronide
-
Substrates: other 7 phenolic compounds show substrate activity on hUGT2A1
Products: -
?
voriconazole + UDP-alpha-D-glucuronate
voriconazole D-glucuronate + UDP
-
Substrates: -
Products: -
?
vorinostat + UDP-glucuronate
UDP + vorinostat beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, P35503, P54855, O75795, P06133, P36537, P35504 Substrates: -
Products: -
?
xanthotoxol + UDP-glucuronate
UDP + xanthotoxol 8-O-glucuronide
zidovudine + UDP-glucuronate
UDP + zidovudine beta-D-glucuronide
Substrates: substrate for isoform UGT2B7
Products: -
?
zidovudine + UDP-glucuronate
UDP + zidovudine O-glucuronide
Substrates: -
Products: -
?
zidovudine + UDP-glucuronate
UDP + zidovudine-5'-glucuronide
Substrates: -
Products: -
?
additional information
?
-
1-hydroxybenzo(a)pyrene + UDP-glucuronate

?
Substrates: UGT1A10 exhibited considerably more glucuronidation activity than any other glucuronosyltransferase UGT1A family member
Products: -
?
1-hydroxybenzo(a)pyrene + UDP-glucuronate
?
Substrates: -
Products: -
?
1-naphthol + UDP-glucuronate

UDP + naphth-1-yl-beta-D-glucuronide
Substrates: -
Products: -
?
1-naphthol + UDP-glucuronate
UDP + naphth-1-yl-beta-D-glucuronide
Substrates: -
Products: -
?
1-naphthol + UDP-glucuronate
UDP + naphth-1-yl-beta-D-glucuronide
-
Substrates: -
Products: -
?
16alpha-hydroxyprogesterone + UDP-glucuronate

?
Substrates: UGT2B15 and UGT2B17 are the major enzyme forms involved in the high-affinity component of 16alpha-hydroxyprogesterone glucuronidation
Products: -
?
16alpha-hydroxyprogesterone + UDP-glucuronate
?
Substrates: -
Products: -
?
16alpha-hydroxyprogesterone + UDP-glucuronate

UDP + 16alpha-hydroxyprgesterone-16-O-D-glucuronate
Substrates: UGT2B15 and UGT2B17 are the major enzyme forms involved in the high-affinity component of 16alpha-hydroxyprogesterone glucuronidation
Products: -
?
16alpha-hydroxyprogesterone + UDP-glucuronate
UDP + 16alpha-hydroxyprgesterone-16-O-D-glucuronate
Substrates: -
Products: -
?
2 UDP-D-glucuronate + 2 dexmedetomidine

2 UDP + dexmedetomidine N1-beta-D-glucuronoside + dexmedetomidine N3-beta-D-glucuronoside
Substrates: the major metabolic pathway of dexmedetomidine, i.e. (4S)-[1-(2,3-dimethylphenyl)ethyl]-1H-imidazole, in humans is N-glucuronidation at the imidazolate nitrogens to N3- and N1-glucuronides
Products: -
?
2 UDP-D-glucuronate + 2 dexmedetomidine
2 UDP + dexmedetomidine N1-beta-D-glucuronoside + dexmedetomidine N3-beta-D-glucuronoside
Substrates: i.e. (+)-4-(S)-[1-(2,3-dimethylphenyl)ethyl]-1H-imidazole, NMR product structure analysis, product ratios of isozyme UGT1A4, overview
Products: -
?
2 UDP-D-glucuronate + 2 dexmedetomidine
2 UDP + dexmedetomidine N1-beta-D-glucuronoside + dexmedetomidine N3-beta-D-glucuronoside
Substrates: i.e. (+)-4-(S)-[1-(2,3-dimethylphenyl)ethyl]-1H-imidazole, NMR product structure analysis, product ratios of isozyme UGT2B10, overview
Products: -
?
2 UDP-D-glucuronate + 2 dexmedetomidine
2 UDP + dexmedetomidine N1-beta-D-glucuronoside + dexmedetomidine N3-beta-D-glucuronoside
Substrates: veryl low activity
Products: -
?
2 UDP-D-glucuronate + 2 dexmedetomidine
2 UDP + dexmedetomidine N1-beta-D-glucuronoside + dexmedetomidine N3-beta-D-glucuronoside
Substrates: low activity
Products: -
?
2 UDP-D-glucuronate + 2 levomedetomidine

2 UDP + levomedetomidine N1-beta-D-glucuronoside + dexmedetomidine N3-beta-D-glucuronoside
Substrates: the major metabolic pathway of levomedetomidine, i.e. (4R)-[1-(2,3-dimethylphenyl)ethyl]-1H-imidazole, in humans is N-glucuronidation at the imidazolate nitrogens to N3-glucuronide
Products: -
?
2 UDP-D-glucuronate + 2 levomedetomidine
2 UDP + levomedetomidine N1-beta-D-glucuronoside + dexmedetomidine N3-beta-D-glucuronoside
Substrates: i.e. (4R)-[1-(2,3-dimethylphenyl)ethyl]-1H-imidazole, NMR product structure analysis, product ratios of isozyme UGT1A4, isozyme UGT1A4 shows low activity producing N1- and N3-glucuronides, overview
Products: -
?
2 UDP-D-glucuronate + 2 levomedetomidine
2 UDP + levomedetomidine N1-beta-D-glucuronoside + dexmedetomidine N3-beta-D-glucuronoside
Substrates: i.e. (4R)-[1-(2,3-dimethylphenyl)ethyl]-1H-imidazole, NMR product structure analysis, product ratios of isozyme UGT2B10, isozyme UGT2B10 exclusively produces N3-glucuronides, overview
Products: -
?
2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid + UDP-glucuronate

?
Substrates: glucuronidation of 2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid is mainly catalyzed by UGT1A1, UGT1A9, and UGT2B7 in the liver, and by UGT1A1, UGT1A3, and UGT2B7 in the intestine i humans
Products: -
?
2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid + UDP-glucuronate
?
Substrates: glucuronidation of 2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid is mainly catalyzed by UGT1A1, UGT1A9, and UGT2B7 in the liver, and by UGT1A1, UGT1A3, and UGT2B7 in the intestine
Products: -
?
2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid + UDP-glucuronate
?
Substrates: -
Products: -
?
2-hydroxyestradiol + UDPglucuronate

UDP + 2-hydroxyestradiol O-glucuronide
-
Substrates: -
Products: -
?
2-hydroxyestradiol + UDPglucuronate
UDP + 2-hydroxyestradiol O-glucuronide
Substrates: -
Products: -
?
2-hydroxyestrone + UDPglucuronate

2-hydroxyestrone 2-O-glucuronide + UDP
-
Substrates: -
Products: -
?
2-hydroxyestrone + UDPglucuronate
2-hydroxyestrone 2-O-glucuronide + UDP
Substrates: -
Products: -
?
2-hydroxyestrone + UDPglucuronate
2-hydroxyestrone 2-O-glucuronide + UDP
-
Substrates: -
Products: -
?
2-hydroxyestrone + UDPglucuronate
2-hydroxyestrone 2-O-glucuronide + UDP
-
Substrates: glucuronidated by UGT1A3 and HGT1A9
Products: -
?
3-hydroxybenzo(a)pyrene + UDP-glucuronate

?
Substrates: UGT1A10 exhibited considerably more glucuronidation activity than any other glucuronosyltransferase UGT1A family member
Products: -
?
3-hydroxybenzo(a)pyrene + UDP-glucuronate
?
Substrates: -
Products: -
?
3-hydroxydesloratadine + UDP-glucuronate

UDP + 3-hydroxydesloratadinyl-O-glucuronide
Substrates: specific substrate of isoform UGT1A8, substrate of isoform UGT1A9 mutant N152A
Products: -
?
3-hydroxydesloratadine + UDP-glucuronate
UDP + 3-hydroxydesloratadinyl-O-glucuronide
Substrates: specific substrate of isoform UGT1A8
Products: -
?
4-hydroxybiphenyl + UDP-glucuronate

UDP + 4-hydroxybiphenyl 4-O-beta-D-glucuronide
-
Substrates: -
Products: -
?
4-hydroxybiphenyl + UDP-glucuronate
UDP + 4-hydroxybiphenyl 4-O-beta-D-glucuronide
-
Substrates: UGT2B7H and UGT2B7Y inactive
Products: -
?
4-hydroxyestradiol + UDPglucuronate

UDP + 4-hydroxyestradiol O-glucuronide
-
Substrates: -
Products: -
?
4-hydroxyestradiol + UDPglucuronate
UDP + 4-hydroxyestradiol O-glucuronide
Substrates: -
Products: -
?
4-hydroxyestrone + UDP-glucuronate

?
Substrates: -
Products: -
?
4-hydroxyestrone + UDP-glucuronate
?
Substrates: -
Products: -
?
4-hydroxyestrone + UDP-glucuronate

UDP + 4-hydroxyestrone 4-O-glucuronide
-
Substrates: -
Products: -
?
4-hydroxyestrone + UDP-glucuronate
UDP + 4-hydroxyestrone 4-O-glucuronide
Substrates: -
Products: -
?
4-hydroxyestrone + UDP-glucuronate
UDP + 4-hydroxyestrone 4-O-glucuronide
-
Substrates: -
Products: -
?
4-methylumbeliferone + UDP-alpha-D-glucuronate

4-methylumbelliferyl-7-O-alpha-D-glucuronide
-
Substrates: -
Products: -
?
4-methylumbeliferone + UDP-alpha-D-glucuronate
4-methylumbelliferyl-7-O-alpha-D-glucuronide
Substrates: -
Products: -
?
4-methylumbeliferone + UDP-alpha-D-glucuronate
4-methylumbelliferyl-7-O-alpha-D-glucuronide
Substrates: -
Products: -
?
4-methylumbeliferone + UDP-alpha-D-glucuronate
4-methylumbelliferyl-7-O-alpha-D-glucuronide
Substrates: -
Products: -
?
4-methylumbeliferone + UDP-alpha-D-glucuronate
4-methylumbelliferyl-7-O-alpha-D-glucuronide
Substrates: -
Products: -
?
4-methylumbelliferone + UDP-glucuronate

UDP + 4-methylumbelliferyl beta-D-glucuronide
-
Substrates: -
Products: -
?
4-methylumbelliferone + UDP-glucuronate
UDP + 4-methylumbelliferyl beta-D-glucuronide
Substrates: -
Products: -
?
4-methylumbelliferone + UDP-glucuronate
UDP + 4-methylumbelliferyl beta-D-glucuronide
Substrates: -
Products: -
?
4-methylumbelliferone + UDP-glucuronate
UDP + 4-methylumbelliferyl beta-D-glucuronide
Substrates: -
Products: -
?
4-methylumbelliferone + UDP-glucuronate

UDP + 4-methylumbelliferyl-7-O-beta-D-glucuronide
-
Substrates: -
Products: -
?
4-methylumbelliferone + UDP-glucuronate
UDP + 4-methylumbelliferyl-7-O-beta-D-glucuronide
Substrates: Phe90 and Phe93 are directly involved in the catalytic activity of UGT1A10 towards 4-methylumbelliferone
Products: -
?
4-methylumbelliferone + UDP-glucuronate
UDP + 4-methylumbelliferyl-7-O-beta-D-glucuronide
Substrates: -
Products: -
?
4-methylumbelliferone + UDP-glucuronate
UDP + 4-methylumbelliferyl-7-O-beta-D-glucuronide
Substrates: -
Products: -
?
4-methylumbelliferone + UDP-glucuronate
UDP + 4-methylumbelliferyl-7-O-beta-D-glucuronide
Substrates: -
Products: -
?
4-methylumbelliferone + UDP-glucuronate
UDP + 4-methylumbelliferyl-7-O-beta-D-glucuronide
Substrates: -
Products: -
?
4-methylumbelliferone + UDP-glucuronate
UDP + 4-methylumbelliferyl-7-O-beta-D-glucuronide
Substrates: -
Products: -
?
4-methylumbelliferone + UDP-glucuronate
UDP + 4-methylumbelliferyl-7-O-beta-D-glucuronide
Substrates: very low rate of glucuronidation
Products: -
?
4-methylumbelliferone + UDP-glucuronate
UDP + 4-methylumbelliferyl-7-O-beta-D-glucuronide
Substrates: -
Products: -
?
4-methylumbelliferone + UDP-glucuronate
UDP + 4-methylumbelliferyl-7-O-beta-D-glucuronide
-
Substrates: -
Products: -
?
4-nitrophenol + UDP-glucuronate

4-nitrophenyl beta-D-glucuronide + UDP
-
Substrates: -
Products: -
?
4-nitrophenol + UDP-glucuronate
4-nitrophenyl beta-D-glucuronide + UDP
Substrates: Phe90 and Phe93 are directly involved in the catalytic activity of UGT1A10 towards 4-nitrophenol
Products: -
?
4-nitrophenol + UDP-glucuronate
4-nitrophenyl beta-D-glucuronide + UDP
Substrates: -
Products: -
?
4-nitrophenol + UDP-glucuronate
4-nitrophenyl beta-D-glucuronide + UDP
Substrates: -
Products: -
?
4-nitrophenol + UDP-glucuronate
4-nitrophenyl beta-D-glucuronide + UDP
Substrates: -
Products: -
?
4-nitrophenol + UDP-glucuronate
4-nitrophenyl beta-D-glucuronide + UDP
Substrates: -
Products: -
?
4-nitrophenol + UDP-glucuronate
4-nitrophenyl beta-D-glucuronide + UDP
-
Substrates: -
Products: -
?
5alpha-androstane-3alpha,17beta-diol + UDP-glucuronate

UDP + 5alpha-androstane-3alpha,17beta-diol O-glucuronide
-
Substrates: -
Products: -
?
5alpha-androstane-3alpha,17beta-diol + UDP-glucuronate
UDP + 5alpha-androstane-3alpha,17beta-diol O-glucuronide
Substrates: -
Products: -
?
7-hydroxy benzo(a)pyrene + UDP-glucuronate

?
Substrates: UGT1A10 exhibited considerably more glucuronidation activity than any other glucuronosyltransferase UGT1A family member
Products: -
?
7-hydroxy benzo(a)pyrene + UDP-glucuronate
?
Substrates: -
Products: -
?
7-hydroxy-4-trifluoromethylcoumarin + UDP-glucuronate

UDP + 7-hydroxy-4-trifluoromethylcoumarin beta-D-glucuronide
Substrates: -
Products: -
?
7-hydroxy-4-trifluoromethylcoumarin + UDP-glucuronate
UDP + 7-hydroxy-4-trifluoromethylcoumarin beta-D-glucuronide
Substrates: -
Products: -
?
9-hydroxybenzo(a)pyrene + UDP-glucuronate

?
Substrates: UGT1A10 exhibited considerably more glucuronidation activity than any other glucuronosyltransferase UGT1A family member
Products: -
?
9-hydroxybenzo(a)pyrene + UDP-glucuronate
?
Substrates: -
Products: -
?
acetaminophen + UDP-glucuronate

?
Substrates: -
Products: -
?
acetaminophen + UDP-glucuronate
?
Substrates: with human UGT1A6, only monoglucuronides are formed, which, however, can be converted to diglucuronides by UGT1A9
Products: -
?
androsterone + UDPglucuronate

UDP + androsterone O-glucuronide
-
Substrates: -
Products: -
?
androsterone + UDPglucuronate
UDP + androsterone O-glucuronide
Substrates: -
Products: -
?
androsterone + UDPglucuronate
UDP + androsterone O-glucuronide
-
Substrates: glucuronidated by HGT2B7H and HGT2B7Y
Products: -
?
anthraflavic acid + UDPglucuronate

UDP + ?
-
Substrates: -
Products: -
?
anthraflavic acid + UDPglucuronate
UDP + ?
-
Substrates: 3 and 7-hydroxyflavone also tested
Products: -
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bakuchiol + UDP-glucuronate

UDP + bakuchiol beta-D-glucuronide
Substrates: bakuchiol is 1-(4-hydroxyphenyl)-3,7-dimethyl-3-vinyl-1,6-octadiene. Isoform UGT2B15 is a main contributor to glucuronidation of bakuchiol
Products: -
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bakuchiol + UDP-glucuronate
UDP + bakuchiol beta-D-glucuronide
Substrates: bakuchiol is 1-(4-hydroxyphenyl)-3,7-dimethyl-3-vinyl-1,6-octadiene. Isoform UGT1A1 is a main contributor to glucuronidation of bakuchiol
Products: -
?
bakuchiol + UDP-glucuronate
UDP + bakuchiol beta-D-glucuronide
Substrates: bakuchiol is 1-(4-hydroxyphenyl)-3,7-dimethyl-3-vinyl-1,6-octadiene. Isoform UGT1A3 is a main contributor to glucuronidation of bakuchiol
Products: -
?
beta-estradiol + UDP-glucuronate

UDP + beta-estradiol-3-glucuronide
Substrates: substrate for isoform UGT1A1
Products: -
?
beta-estradiol + UDP-glucuronate
UDP + beta-estradiol-3-glucuronide
Substrates: -
Products: -
?
bilirubin + UDPglucuronate

bilirubin monoglucuronoside + bilirubin diglucuronoside + UDP
-
Substrates: -
Products: -
?
bilirubin + UDPglucuronate
bilirubin monoglucuronoside + bilirubin diglucuronoside + UDP
Substrates: -
Products: -
?
borneol + UDPglucuronate

UDP + borneol O-glucuronide
-
Substrates: -
Products: -
?
borneol + UDPglucuronate
UDP + borneol O-glucuronide
-
Substrates: other 4 monoterpenoid tested on hUGT2A1
Products: -
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C-1748 + UDP-glucuronate

UDP + C-1748 O-glucuronide
Substrates: C-1748 is 9-(2'-hydroxyethylamino)-4-methyl-1-nitroacridine. The reaction is selectively catalyzed by isoform UGT2B17
Products: -
?
C-1748 + UDP-glucuronate
UDP + C-1748 O-glucuronide
Substrates: C-1748 is 9-(2'-hydroxyethylamino)-4-methyl-1-nitroacridine. The reaction is selectively catalyzed by isoform UGT2B7
Products: -
?
chenodeoxycholic acid + UDP-glucuronate

UDP + ?
-
Substrates: -
Products: -
?
chenodeoxycholic acid + UDP-glucuronate
UDP + ?
-
Substrates: low activity in patients with liver cirrhosis and granulomatous hepatitis
Products: -
?
chenodeoxycholic acid + UDP-glucuronate
UDP + ?
Substrates: substrate for isoform UGT1A3
Products: -
?
epirubicin + UDP-glucuronate

UDP + epirubicin beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, P35503, P54855, O75795, P06133, P36537, P35504 Substrates: -
Products: -
?
epirubicin + UDP-glucuronate
UDP + epirubicin beta-D-glucuronoside
Substrates: substrate for isoform UGT2B7
Products: -
?
epitestosterone + UDP-glucuronate

UDP + epitestosterone 17-O-glucuronide
Substrates: -
Products: -
?
epitestosterone + UDP-glucuronate
UDP + epitestosterone 17-O-glucuronide
-
Substrates: epitestosterone glucuronidation is catalyzed mainly by UGT2B7. No substrate for isoform UGT2B17, but it binds epitestosterone with affinity similar to that of testosterone. Isoform UGT2A1 catalyzes the glucuronidation of both steroids at considerable rates and similar kinetics
Products: -
?
estriol + UDP-glucuronate

?
Substrates: -
Products: -
?
estriol + UDP-glucuronate
?
Substrates: metabilized by mutant enzyme S432G-UGT1A7, but not by wild-type enzyme UGT1A7
Products: -
?
estriol + UDPglucuronate

UDP + estriol-16 alpha-glucuronide
-
Substrates: -
Products: -
?
estriol + UDPglucuronate
UDP + estriol-16 alpha-glucuronide
-
Substrates: catalyzed by isozyme 1 but not by isozyme 2
Products: -
?
estriol + UDPglucuronate
UDP + estriol-16 alpha-glucuronide
-
Substrates: UGT1A3 inactive
Products: -
?
estrogen + UDP-glucuronate

?
Substrates: UDP-glucuronosyltransferase 1A10 has been identified as the major isoform involved in the biotransformation of a wide range of phenolic substrates, including native estrogens and their oxidized metabolites
Products: -
?
estrogen + UDP-glucuronate
?
Substrates: phenylalanine(90) and phenylalanine(93) are crucial amino acids within the estrogen binding site of the human UDP-glucuronosyltransferase 1A10
Products: -
?
estrone + UDPglucuronate

UDP + estrone 3-O-glucuronide
-
Substrates: glucuronidated by UGT1A3 and HGT1A9
Products: -
?
estrone + UDPglucuronate
UDP + estrone 3-O-glucuronide
-
Substrates: inactive
Products: -
?
etoposide + UDP-glucuronate

UDP + etoposide glucuronide
Substrates: UGT1A1 is principally responsible for the formation of etoposide glucuronides, mainly in the form of phenolic glucuronide
Products: -
?
etoposide + UDP-glucuronate
UDP + etoposide glucuronide
Substrates: -
Products: -
?
etoposide + UDP-glucuronate
UDP + etoposide glucuronide
Substrates: activity with UGT1A3 is much lower than activity with UGT1A1
Products: -
?
etoposide + UDP-glucuronate
UDP + etoposide glucuronide
Substrates: activity with UGT1A8 is much lower than activity with UGT1A1
Products: -
?
hyodeoxycholic acid + UDP-glucuronate

?
Substrates: -
Products: -
?
hyodeoxycholic acid + UDP-glucuronate
?
Substrates: -
Products: -
?
lithocholic acid + UDPglucuronate

UDP + ?
-
Substrates: -
Products: -
?
lithocholic acid + UDPglucuronate
UDP + ?
-
Substrates: highest activity among five bile acids studied
Products: -
?
morphine + UDP-glucuronate

UDP + morphine 3,6-diglucuronide
-
Substrates: -
Products: -
?
morphine + UDP-glucuronate
UDP + morphine 3,6-diglucuronide
Substrates: -
Products: -
?
morphine + UDP-glucuronate
UDP + morphine 3,6-diglucuronide
-
Substrates: substrate for UGT2B7
Products: -
?
morphine + UDP-glucuronate
UDP + morphine 3,6-diglucuronide
-
Substrates: glucuronidated by HGT2B7H and HGT2B7Y at 3 and 6 hydroxy positions
Products: -
?
propofol + UDP-alpha-D-glucuronate

UDP + propofol D-glucuronide
-
Substrates: substrate of isoform UGT1A9
Products: -
?
propofol + UDP-alpha-D-glucuronate
UDP + propofol D-glucuronide
-
Substrates: -
Products: -
?
scopoletin + UDP-glucuronate

UDP + scopoletin O-glucuronide
Substrates: -
Products: -
?
scopoletin + UDP-glucuronate
UDP + scopoletin O-glucuronide
Substrates: very low rate of glucuronidation
Products: -
?
scopoletin + UDP-glucuronate
UDP + scopoletin O-glucuronide
-
Substrates: -
Products: -
?
scopoletin + UDPglucuronate

UDP + scopoletin O-glucuronide
-
Substrates: -
Products: -
?
scopoletin + UDPglucuronate
UDP + scopoletin O-glucuronide
Substrates: -
Products: -
?
scopoletin + UDPglucuronate
UDP + scopoletin O-glucuronide
-
Substrates: -
Products: -
?
scopoletin + UDPglucuronate
UDP + scopoletin O-glucuronide
-
Substrates: other 3 coumarines show substrate activity on hUGT2A1
Products: -
?
serotonin + UDP-glucuronate

UDP + 3-(2-aminoethyl)-1H-indol-5-yl beta-D-glucuronide
Substrates: highly selective substrate of UGT1A6 in human liver microsomes, with human UGT1A6, only monoglucuronides are formed, which, however, can be converted to diglucuronides by UGT1A9
Products: -
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serotonin + UDP-glucuronate
UDP + 3-(2-aminoethyl)-1H-indol-5-yl beta-D-glucuronide
Substrates: coexpression of UGT1A6 with UGT2B7 influences wild-type UGT1A6, increasing the normalized activity of UGT1A6
Products: -
?
serotonin + UDP-glucuronate
UDP + 3-(2-aminoethyl)-1H-indol-5-yl beta-D-glucuronide
-
Substrates: -
Products: -
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serotonin + UDP-glucuronate

UDP + serotonin beta-D-glucuronide
P16662, P19224, O60656, P22309, P22310, P35503, P54855, O75795, P06133, P36537, P35504 Substrates: -
Products: -
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serotonin + UDP-glucuronate
UDP + serotonin beta-D-glucuronide
Substrates: substrate for isoform UGT1A6
Products: -
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testosterone + UDP-glucuronate

UDP + testosterone beta-D-glucuronoside
Substrates: UGT2B15 and UGT2B17 are the major enzyme forms involved in human liver microsomal testosterone 17beta-glucuronidation
Products: -
?
testosterone + UDP-glucuronate
UDP + testosterone beta-D-glucuronoside
Substrates: -
Products: -
?
testosterone + UDP-glucuronate
UDP + testosterone beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, P35503, P54855, O75795, P06133, P36537, P35504 Substrates: -
Products: -
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UDP-alpha-D-glucuronate + (R)-propranolol

UDP + (R)-propranolol beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-alpha-D-glucuronate + (R)-propranolol
UDP + (R)-propranolol beta-D-glucuronoside
Substrates: high activity
Products: -
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UDP-alpha-D-glucuronate + (S)-propranolol

UDP + (S)-propranolol beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-alpha-D-glucuronate + (S)-propranolol
UDP + (S)-propranolol beta-D-glucuronoside
Substrates: high activity
Products: -
?
UDP-D-glucuronate + 1-naphthol

UDP + 1-naphthyl beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + 1-naphthol
UDP + 1-naphthyl beta-D-glucuronoside
Substrates: isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + 1-naphthol
UDP + 1-naphthyl beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + 1-naphthol
UDP + 1-naphthyl beta-D-glucuronoside
Substrates: reaction of isozyme UGT1A6
Products: -
?
UDP-D-glucuronate + 2-naphthol

UDP + 2-naphthyl beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + 2-naphthol
UDP + 2-naphthyl beta-D-glucuronoside
Substrates: isozyme UGT1A7
Products: -
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UDP-D-glucuronate + 4-hydroxy-N-desmethyl-tamoxifen

UDP + 4-hydroxy-N-desmethyl-tamoxifen beta-D-glucuronoside
Substrates: the enzyme is involved in metabolism and elimination of tamoxifen, TAM, and its major active metabolites 4-hydroxytamoxifen and 4-hydroxy-N-desmethyl-tamoxifen, i.e. endoxifen, by glucuronidation, overview
Products: -
?
UDP-D-glucuronate + 4-hydroxy-N-desmethyl-tamoxifen
UDP + 4-hydroxy-N-desmethyl-tamoxifen beta-D-glucuronoside
Substrates: i.e. endoxifen, substrate synthesis, overview, O-glucuronidation by liver microsomes
Products: product identification by HPLC and mass spectrometry analysis
?
UDP-D-glucuronate + 4-methylumbelliferone

UDP + 4-methylumbelliferone beta-D-glucuronoside
Substrates: non-selective substrate
Products: -
?
UDP-D-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferone beta-D-glucuronoside
Substrates: isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferone beta-D-glucuronoside
Substrates: isozyme UGT1A6
Products: -
?
UDP-D-glucuronate + 4-methylumbelliferone

UDP + 4-methylumbelliferyl beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferyl beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferyl beta-D-glucuronoside
Substrates: isozyme UGT1A6
Products: -
?
UDP-D-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferyl beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferyl beta-D-glucuronoside
Substrates: recombinant isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + 4-nitrophenol

UDP + 4-nitrophenyl beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + 4-nitrophenol
UDP + 4-nitrophenyl beta-D-glucuronoside
Substrates: isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + 4-nitrophenol
UDP + 4-nitrophenyl beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + 6-hydroxy-warfarin

UDP + 6-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + 6-hydroxy-warfarin
UDP + 6-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A10
Products: -
?
UDP-D-glucuronate + 7-hydroxy-warfarin

UDP + 7-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + 7-hydroxy-warfarin
UDP + 7-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A10
Products: -
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UDP-D-glucuronate + 8-hydroxy-warfarin

UDP + 8-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A9
Products: -
?
UDP-D-glucuronate + 8-hydroxy-warfarin
UDP + 8-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + 8-hydroxy-warfarin
UDP + 8-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A10
Products: -
?
UDP-D-glucuronate + acceptor

UDP + acceptor beta-D-glucuronoside
Substrates: the enzyme plays a key role in the metabolism of endogenous and exogenous compounds
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
-
Substrates: glucuronidation is a major phase II conjugation reaction of numerous xenobiotic as well as endobiotic compounds
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
-
Substrates: protein kinases are involved in UGT regulation, UGTs inactivate aromatic-like metabolites and a vast number of dietary and environmental chemicals, which reduces the risk of toxicities, mutagenesis, and carcinogenesis, primarily in liver, kidney, and gastrointestinal tract, overview
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
-
Substrates: potential role of UGTs in regulating aldosterone
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: conjugation by UDP-glucuronosyltransferase is the major pathway of androgen metabolism and elimination in the human
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
-
Substrates: UDP-glucuronosyltransferases play important roles in the metabolism, detoxification,and clearance of many different xenobiotics, including drugs and endogenous compounds
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: UGT isozyme substrate specificity, overview
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: UDP-glucuronosyltransferases are membrane-bound proteins localized to the endoplasmic reticulum and catalyze the formation of beta-D-glucopyranosiduronic acids using UDP-D-glucuronic acid and acceptor substrates such as drugs, steroids, bile acids, xenobiotics, and dietary nutrients
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: the enzyme is involved in detoxification reactions
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: the recombinant isozyme 2A3, expressed in insect cells via baculovirus system, selectively glucuronidates bile acids, particularly hyodeoxycholic acid at the 6-hydroxy position, wide substrate specificity, detailed overview
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
-
Substrates: UGTs contain a Rossman fold motif predicted to bind the UDP-containing sugar donor substrate
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: differences in substrate binding between isozymes of different oligomeric state, overview
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + androstane-3alpha,17beta-diol

UDP + ?
Substrates: in epithelial cells of the human prostate
Products: -
?
UDP-D-glucuronate + androstane-3alpha,17beta-diol
UDP + ?
Substrates: isozyme UGT2B7in the liver
Products: -
?
UDP-D-glucuronate + androstane-3alpha,17beta-diol
UDP + ?
Substrates: isozyme UGT2B15 in the liver
Products: -
?
UDP-D-glucuronate + androstane-3alpha,17beta-diol
UDP + ?
Substrates: isozyme UGT2B17 in the liver
Products: -
?
UDP-D-glucuronate + androstane-3alpha,17beta-diol
UDP + ?
Substrates: -
Products: -
?
UDP-D-glucuronate + androstane-3alpha,17beta-diol
UDP + ?
Substrates: isozyme UGT2B7
Products: -
?
UDP-D-glucuronate + androstane-3alpha,17beta-diol
UDP + ?
Substrates: isozyme UGT2B15
Products: -
?
UDP-D-glucuronate + androstane-3alpha,17beta-diol
UDP + ?
Substrates: isozyme UGT2B17
Products: -
?
UDP-D-glucuronate + androstane-3alpha,17beta-diol
UDP + ?
Substrates: -
Products: -
?
UDP-D-glucuronate + androsterone

UDP + androsterone 3-O-beta-D-glucuronoside
Substrates: in epithelial cells of the human prostate
Products: -
?
UDP-D-glucuronate + androsterone
UDP + androsterone 3-O-beta-D-glucuronoside
Substrates: isozyme UGT2B7in the liver
Products: -
?
UDP-D-glucuronate + androsterone
UDP + androsterone 3-O-beta-D-glucuronoside
Substrates: isozyme UGT2B15 in the liver
Products: -
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UDP-D-glucuronate + androsterone
UDP + androsterone 3-O-beta-D-glucuronoside
Substrates: isozyme UGT2B17 in the liver
Products: -
?
UDP-D-glucuronate + androsterone
UDP + androsterone 3-O-beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + androsterone
UDP + androsterone 3-O-beta-D-glucuronoside
Substrates: isozyme UGT2B7
Products: -
?
UDP-D-glucuronate + androsterone
UDP + androsterone 3-O-beta-D-glucuronoside
Substrates: isozyme UGT2B15
Products: -
?
UDP-D-glucuronate + androsterone
UDP + androsterone 3-O-beta-D-glucuronoside
Substrates: isozyme UGT2B17
Products: -
?
UDP-D-glucuronate + cis-4-hydroxytamoxifen

UDP + 4-hydroxytamoxifen beta-D-glucuronoside
Substrates: the enzyme is involved in metabolism and elimination of tamoxifen, TAM, and its major active metabolites 4-hydroxytamoxifen and 4-hydroxy-N-desmethyl-tamoxifen, i.e. endoxifen, by glucuronidation, overview
Products: -
?
UDP-D-glucuronate + cis-4-hydroxytamoxifen
UDP + 4-hydroxytamoxifen beta-D-glucuronoside
Substrates: N- and O-glucuronidation by liver microsomes
Products: product identification by HPLC and mass spectrometry analysis
?
UDP-D-glucuronate + cotinine

UDP + ?
Substrates: isozyme UGT2B10, cotinine is exclusively glucuronized in liver, no activity in intestinal microsomes
Products: -
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UDP-D-glucuronate + cotinine
UDP + ?
Substrates: isozyme UGT1A4
Products: -
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UDP-D-glucuronate + cotinine
UDP + ?
Substrates: isozyme UGT2B10
Products: -
?
UDP-D-glucuronate + curcumin

UDP + curcumin beta-D-glucuronoside
-
Substrates: low activity, can reverse the inhibitory effect of curcumin on UGTs
Products: -
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UDP-D-glucuronate + curcumin
UDP + curcumin beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + curcumin

UDP + curcumin phenolic beta-D-monoglucuronide
-
Substrates: glucuronidation is an important pathway in the metabolism of curcumin
Products: -
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UDP-D-glucuronate + curcumin
UDP + curcumin phenolic beta-D-monoglucuronide
-
Substrates: -
Products: -
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UDP-D-glucuronate + dehydrotestosterone

UDP + dehydrotestosterone 17-O-beta-D-glucuronoside
Substrates: isozyme UGT2B7in the liver
Products: -
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UDP-D-glucuronate + dehydrotestosterone
UDP + dehydrotestosterone 17-O-beta-D-glucuronoside
Substrates: isozyme UGT2B15in the liver
Products: -
?
UDP-D-glucuronate + dehydrotestosterone
UDP + dehydrotestosterone 17-O-beta-D-glucuronoside
Substrates: isozyme UGT2B17in the liver
Products: -
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UDP-D-glucuronate + dehydrotestosterone
UDP + dehydrotestosterone 17-O-beta-D-glucuronoside
Substrates: isozyme UGT2B7
Products: -
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UDP-D-glucuronate + dehydrotestosterone
UDP + dehydrotestosterone 17-O-beta-D-glucuronoside
Substrates: isozyme UGT2B15
Products: -
?
UDP-D-glucuronate + dehydrotestosterone
UDP + dehydrotestosterone 17-O-beta-D-glucuronoside
Substrates: isozyme UGT2B17
Products: -
?
UDP-D-glucuronate + dihydrotestosterone

UDP + dihydrotestosterone 17-O-beta-D-glucuronoside
Substrates: in epithelial cells of the human prostate
Products: -
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UDP-D-glucuronate + dihydrotestosterone
UDP + dihydrotestosterone 17-O-beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + estradiol

UDP + estradiol 3-O-beta-D-glucuronoside
-
Substrates: isozymes UGT1A1 and UGT1A9
Products: -
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UDP-D-glucuronate + estradiol
UDP + estradiol 3-O-beta-D-glucuronoside
Substrates: reaction of isozyme UGT1A1
Products: -
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UDP-D-glucuronate + estradiol

UDP + estradiol-3-beta-D-glucuronoside
Substrates: liver microsomes
Products: -
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UDP-D-glucuronate + estradiol
UDP + estradiol-3-beta-D-glucuronoside
Substrates: recombinant isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + eugenol

UDP + eugenol beta-D-glucuronoside
Substrates: isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + eugenol
UDP + eugenol beta-D-glucuronoside
-
Substrates: -
Products: -
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UDP-D-glucuronate + frusemide

UDP + frusemide beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + frusemide
UDP + frusemide beta-D-glucuronoside
-
Substrates: substrate of isozymes UGT 1A1, UGT1A3, UGT1A6, UGT1A7, UGT1A9, UGT1A10 and UGT2B7, with a predominant role of UGT1A9 in liver and kidney
Products: -
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UDP-D-glucuronate + gemfibrozil

UDP + gemfibrozil beta-D-glucuronoside
-
Substrates: gemfibrozil is a fibrate hypolipidemic agent, isozyme UGT2B7 in the liver
Products: -
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UDP-D-glucuronate + gemfibrozil
UDP + gemfibrozil beta-D-glucuronoside
-
Substrates: activity with isozymes UGT1A1, UGT1A3, UGT1A9, UGT2B4, UGT2B7, UGT2B17, and especially with isozyme UGT2B7 showing the highest activity
Products: -
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UDP-D-glucuronate + hyodeoxycholic acid

UDP + hyodeoxycholic acid 6-O-glucuronoside
Substrates: isozyme UGT2A3
Products: -
?
UDP-D-glucuronate + hyodeoxycholic acid
UDP + hyodeoxycholic acid 6-O-glucuronoside
Substrates: recombinant enzyme, expressed in insect cells via baculovirus system, selective glucuronidation
Products: product formation depends on the isozyme, overview
?
UDP-D-glucuronate + labetalol

UDP + ?
Substrates: the reaction is catalyzed mainly by isozymes UGT1A1 and UGT2B7, potential role for progesterone in regulating labetalol elimination by modulating the expression of UGT1A1, leading to enhanced drug metabolism during pregnancy, overview
Products: -
?
UDP-D-glucuronate + labetalol
UDP + ?
Substrates: -
Products: -
?
UDP-D-glucuronate + labetalol
UDP + ?
Substrates: the reaction is catalyzed mainly by isozymes UGT1A1 and UGT2B7, overview
Products: -
?
UDP-D-glucuronate + menadiol

UDP + mendadiol 1-O-beta-D-glucuronoside
-
Substrates: -
Products: isoform UGT1A6, formation of 1-menadiol glucuronide and 4-menadiol glucuronide in ratio of about 4:1
?
UDP-D-glucuronate + menadiol
UDP + mendadiol 1-O-beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + menadiol

UDP + mendadiol 4-O-beta-D-glucuronoside
-
Substrates: -
Products: isoform UGT1A6, formation of 1-menadiol glucuronide and 4-menadiol glucuronide in ratio of about 4:1
?
UDP-D-glucuronate + menadiol
UDP + mendadiol 4-O-beta-D-glucuronoside
-
Substrates: -
Products: isoform UGT1A10, preferential formation of 4-menadiol glucuronoside
?
UDP-D-glucuronate + morphine

UDP + morphine 3-O-beta-D-glucuronoside
-
Substrates: isozyme UGT2B7
Products: -
?
UDP-D-glucuronate + morphine
UDP + morphine 3-O-beta-D-glucuronoside
Substrates: isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + morphine

UDP + morphine 6-beta-D-glucuronoside
Substrates: the metabolic conversion of morphine to morphine-6-glucuronide plays a significant role in mediation of the clinical effect of morphine because of the superior analgesic effect of morphine-6-glucuronide
Products: -
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UDP-D-glucuronate + morphine
UDP + morphine 6-beta-D-glucuronoside
Substrates: isozyme UGT1A8, as the morphine concentration approaches 0.1 mM, morphine-6-glucuronidation activity gradually decreases, and the kinetics closely resemble substrate inhibition Michaelis-Menten kinetic behavior
Products: -
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UDP-D-glucuronate + morphine
UDP + morphine 6-beta-D-glucuronoside
Substrates: isozyme UGT1A1, as the morphine concentration approaches 0.1 mM, morphine-6-glucuronidation activity gradually decreases, and the kinetics closely resemble substrate inhibition Michaelis-Menten kinetic behavior
Products: -
?
UDP-D-glucuronate + nicotine

UDP + ?
Substrates: isozyme UGT2B10, nicotine is mainly glucuronized in liver, very low activity in intestinal microsomes
Products: -
?
UDP-D-glucuronate + nicotine
UDP + ?
Substrates: isozyme UGT1A4
Products: -
?
UDP-D-glucuronate + nicotine
UDP + ?
Substrates: isozyme UGT2B10
Products: -
?
UDP-D-glucuronate + nicotine
UDP + ?
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
?
UDP-D-glucuronate + octylgallate

UDP + octylgallate beta-D-glucuronoside
Substrates: isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + octylgallate
UDP + octylgallate beta-D-glucuronoside
Substrates: isozyme UGT1A1
Products: -
?
UDP-D-glucuronate + octylgallate
UDP + octylgallate beta-D-glucuronoside
Substrates: isozyme UGT1A3
Products: -
?
UDP-D-glucuronate + propofol

UDP + propofol beta-D-glucuronoside
-
Substrates: isozymes UGT1A1 and UGT1A9
Products: -
?
UDP-D-glucuronate + propofol
UDP + propofol beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + propofol
UDP + propofol beta-D-glucuronoside
Substrates: -
Products: -
?
UDP-D-glucuronate + propofol
UDP + propofol beta-D-glucuronoside
-
Substrates: -
Products: -
?
UDP-D-glucuronate + protocatechuic aldehyde

UDP + ?
Substrates: -
Products: -
?
UDP-D-glucuronate + protocatechuic aldehyde
UDP + ?
Substrates: i.e. 3,4-dihydroxybenzaldehyde, the reaction is catalyzed by recombinant isozyme UGT1A6, especially, and also by isozyme UGT1A9, as well as by liver and intestine microsomes, overview
Products: -
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UDP-D-glucuronate + scopoletin

UDP + scopoletin beta-D-glucuronoside
Substrates: isozyme UGT1A1
Products: -
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UDP-D-glucuronate + scopoletin
UDP + scopoletin beta-D-glucuronoside
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Substrates: substrate binding structure, UGT1A6 residues His371 and Glu379 are directly involved in UDPGA binding but are not the general acid or general base, homology mocelling, overview
Products: -
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UDP-D-glucuronate + scopoletin
UDP + scopoletin beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + tamoxifen + H+

UDP + tamoxifen beta-D-glucuronoside
Substrates: the enzyme is involved in metabolism and elimination of tamoxifen, TAM, and its major active metabolites 4-hydroxytamoxifen and 4-hydroxy-N-desmethyl-tamoxifen, i.e. endoxifen, by glucuronidation, overview
Products: -
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UDP-D-glucuronate + tamoxifen + H+
UDP + tamoxifen beta-D-glucuronoside
Substrates: N- and O-glucuronidation by liver microsomes
Products: product identification by HPLC and mass spectrometry analysis
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UDP-D-glucuronate + thyroxine

UDP + thyroxine beta-D-glucuronoside
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Substrates: glucuronidation of the thyroid hormone thyroxine, T4, in the human liver, the T4 glucuronidation activities of recombinant human UGT isoforms and microsomes
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UDP-D-glucuronate + thyroxine
UDP + thyroxine beta-D-glucuronoside
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Substrates: -
Products: -
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UDP-D-glucuronate + trans-4-hydroxytamoxifen

UDP + 4-hydroxytamoxifen beta-D-glucuronoside
Substrates: the enzyme is involved in metabolism and elimination of tamoxifen, TAM, and its major active metabolites 4-hydroxytamoxifen and 4-hydroxy-N-desmethyl-tamoxifen, i.e. endoxifen, by glucuronidation, overview
Products: -
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UDP-D-glucuronate + trans-4-hydroxytamoxifen
UDP + 4-hydroxytamoxifen beta-D-glucuronoside
Substrates: N- and O-glucuronidation by liver microsomes
Products: product identification by HPLC and mass spectrometry analysis
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UDP-D-glucuronate + trans-4-hydroxytamoxifen
UDP + 4-hydroxytamoxifen beta-D-glucuronoside
Substrates: N- and O-glucuronidation by liver microsomes, no activity by isozyme UGT2B15
Products: product identification by HPLC and mass spectrometry analysis
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UDP-D-glucuronate + zidovudine

UDP + zidovudine beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + zidovudine
UDP + zidovudine beta-D-glucuronoside
Substrates: an UGT2B7 substrate
Products: -
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UDP-D-glucuronate + zidovudine
UDP + zidovudine beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + zidovudine
UDP + zidovudine beta-D-glucuronoside
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Substrates: -
Products: -
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UDP-glucuronate + (E)-2,4-dimethoxy-6-(4-methoxystyryl)benzaldehyde oxime

UDP + 1-O-[(E)-2,4-dimethoxy-6-(4-methoxystyryl)benzaldehyde oxime]-beta-D-glucuronate
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Substrates: i.e. NI-ST-05, low activity, NI-ST-05 forms a distinct N-O-glucuronide. NI-ST-05 is primarily metabolized by an extrahepatic enzyme, UGT1A10
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UDP-glucuronate + (E)-2,4-dimethoxy-6-(4-methoxystyryl)benzaldehyde oxime
UDP + 1-O-[(E)-2,4-dimethoxy-6-(4-methoxystyryl)benzaldehyde oxime]-beta-D-glucuronate
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Substrates: i.e. NI-ST-05, low activity, NI-ST-05 forms a distinct N-O-glucuronide. NI-ST-05 is primarily metabolized by an extrahepatic enzyme, UGT1A10, in cooperative binding
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UDP-glucuronate + 1-naphthol

UDP + 1-naphthol beta-D-glucuronide
Substrates: isozyme UGT1A1
Products: -
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UDP-glucuronate + 1-naphthol
UDP + 1-naphthol beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + 1-naphthol
UDP + 1-naphthol beta-D-glucuronide
Substrates: isozyme UGT1A3
Products: -
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UDP-glucuronate + 1-naphthol
UDP + 1-naphthol beta-D-glucuronide
Substrates: isozyme UGT1A6
Products: -
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UDP-glucuronate + 1-naphthol
UDP + 1-naphthol beta-D-glucuronide
Substrates: isozyme UGT1A7
Products: -
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UDP-glucuronate + 1-naphthol
UDP + 1-naphthol beta-D-glucuronide
Substrates: isozyme UGT1A8
Products: -
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UDP-glucuronate + 1-naphthol
UDP + 1-naphthol beta-D-glucuronide
Substrates: isozyme UGT1A9
Products: -
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UDP-glucuronate + 1-naphthol
UDP + 1-naphthol beta-D-glucuronide
Substrates: isozyme UGT1A10
Products: -
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UDP-glucuronate + 1-naphthol
UDP + 1-naphthol beta-D-glucuronide
Substrates: isozyme UGT2B7
Products: -
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UDP-glucuronate + 17-alpha-estradiol

UDP + 17-alpha-estradiol 3-O-beta-D-glucuronoside
Substrates: lower activity
Products: -
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UDP-glucuronate + 17-alpha-estradiol
UDP + 17-alpha-estradiol 3-O-beta-D-glucuronoside
Substrates: very low activity
Products: -
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UDP-glucuronate + 17-alpha-estradiol
UDP + 17-alpha-estradiol 3-O-beta-D-glucuronoside
Substrates: low activity
Products: -
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UDP-glucuronate + 17-alpha-estradiol
UDP + 17-alpha-estradiol 3-O-beta-D-glucuronoside
Substrates: very high activity with UGT1A10
Products: -
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UDP-glucuronate + 17-beta-estradiol

UDP + 17-beta-estradiol 3-O-beta-D-glucuronoside
Substrates: lower activity
Products: -
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UDP-glucuronate + 17-beta-estradiol
UDP + 17-beta-estradiol 3-O-beta-D-glucuronoside
Substrates: low activity
Products: -
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UDP-glucuronate + 17-beta-estradiol
UDP + 17-beta-estradiol 3-O-beta-D-glucuronoside
Substrates: very high activity
Products: -
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UDP-glucuronate + 2',4,4',6'-tetrahydroxychalcone

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Substrates: isozyme UGT1A7
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UDP-glucuronate + 2',4,4',6'-tetrahydroxychalcone
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Substrates: isozyme UGT1A1
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UDP-glucuronate + 2',4,4',6'-tetrahydroxychalcone
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Substrates: isozymes UGT1A1, UGT1A7, and UGT1A10
Products: -
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UDP-glucuronate + 20-hydroxyeicosatetraenoic acid

UDP + 20-hydroxyeicosatetraenoyl beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
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UDP-glucuronate + 20-hydroxyeicosatetraenoic acid
UDP + 20-hydroxyeicosatetraenoyl beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + 3,2'-dihydroxychalcone

UDP + 3-hydroxychalcone 2'-O-beta-D-glucuronoside
-
Substrates: glucuronidation at the OH-2' position by UGT1A8 isoform
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UDP-glucuronate + 3,2'-dihydroxychalcone
UDP + 3-hydroxychalcone 2'-O-beta-D-glucuronoside
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Substrates: very low activity with isozyme UGT1A6
Products: -
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UDP-glucuronate + 3-epideacetycinobufagin

UDP + 3-epideacetycinobufagin 3-beta-D-glucuronoside
Substrates: 3-epideacetycinobufagin is a highly isoform-specific probe substrate for 3-glucuronidation mediated by UDP-glucuronosyltransferase 2B7 determined in recombinant UGT supersomes, overview
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UDP-glucuronate + 3-epideacetycinobufagin
UDP + 3-epideacetycinobufagin 3-beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + 4-methylumbelliferone

UDP + 4-methylumbelliferone beta-D-glucuronide
Substrates: isozyme UGT1A1
Products: -
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UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferone beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferone beta-D-glucuronide
Substrates: isozyme UGT1A3
Products: -
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UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferone beta-D-glucuronide
Substrates: isozyme UGT1A6
Products: -
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UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferone beta-D-glucuronide
Substrates: isozyme UGT1A7
Products: -
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UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferone beta-D-glucuronide
Substrates: isozyme UGT1A8
Products: -
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UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferone beta-D-glucuronide
Substrates: isozyme UGT1A9
Products: -
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UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferone beta-D-glucuronide
Substrates: isozyme UGT1A10
Products: -
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UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferone beta-D-glucuronide
Substrates: isozyme UGT2B7
Products: -
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UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferone beta-D-glucuronide
Substrates: isozyme UGT2B15
Products: -
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UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferone beta-D-glucuronide
Substrates: isozyme UGT2B17
Products: -
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UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferone beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + 4-methylumbelliferone

UDP + 4-methylumbelliferyl beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + 4-methylumbelliferone
UDP + 4-methylumbelliferyl beta-D-glucuronoside
Substrates: high activity
Products: -
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UDP-glucuronate + acceptor

UDP + acceptor beta-D-glucuronoside
Substrates: UGT1A10 is an important detoxifier of polycyclic aromatic hydrocarbons
Products: -
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UDP-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + acceptor

UDP + acceptor beta-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + acceptor
UDP + acceptor beta-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + acceptor
UDP + acceptor beta-glucuronoside
Substrates: differences in substrate binding between isozymes of different oligomeric state, overview
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UDP-glucuronate + anthraflavic acid

UDP + anthraflavic acid 2-O-beta-D-glucuronide
Substrates: isozyme UGT1A9
Products: -
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UDP-glucuronate + anthraflavic acid
UDP + anthraflavic acid 2-O-beta-D-glucuronide
Substrates: isozyme UGT1A1
Products: -
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UDP-glucuronate + anthraflavic acid
UDP + anthraflavic acid 2-O-beta-D-glucuronide
Substrates: isozymes UGT1A1, and UGT1A9
Products: -
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UDP-glucuronate + apigenin

UDP + apigenin beta-D-glucuronide
Substrates: isozyme UGT1A7
Products: -
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UDP-glucuronate + apigenin
UDP + apigenin beta-D-glucuronide
Substrates: isozyme UGT1A1
Products: -
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UDP-glucuronate + apigenin
UDP + apigenin beta-D-glucuronide
Substrates: isozymes UGT1A1, UGT1A7, and UGT1A10
Products: -
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UDP-glucuronate + bilirubin

UDP + bilirubin beta-D-glucuronoside
Substrates: very high activity
Products: -
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UDP-glucuronate + bilirubin
UDP + bilirubin beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + biochanin A

UDP + biochanin A beta-D-glucuronide
Substrates: isozyme UGT1A7
Products: -
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UDP-glucuronate + biochanin A
UDP + biochanin A beta-D-glucuronide
Substrates: isozyme UGT1A1
Products: -
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UDP-glucuronate + biochanin A
UDP + biochanin A beta-D-glucuronide
Substrates: isozymes UGT1A1, UGT1A7, and UGT1A10
Products: -
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UDP-glucuronate + capsaicin

UDP + capsaicin beta-D-glucuronide
Substrates: isozyme UGT1A7
Products: -
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UDP-glucuronate + capsaicin
UDP + capsaicin beta-D-glucuronide
Substrates: isozyme UGT1A1
Products: -
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UDP-glucuronate + capsaicin
UDP + capsaicin beta-D-glucuronide
Substrates: isozymes UGT1A1, UGT1A7, and UGT1A10
Products: -
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UDP-glucuronate + chenodeoxycholic acid

UDP + chenodeoxycholic acid 24-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
Products: -
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UDP-glucuronate + chenodeoxycholic acid
UDP + chenodeoxycholic acid 24-beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + chenodeoxycholic acid
UDP + chenodeoxycholic acid 24-beta-D-glucuronoside
Substrates: best substrate
Products: -
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UDP-glucuronate + cholic acid

UDP + cholic acid 24-beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + cholic acid
UDP + cholic acid 24-beta-D-glucuronoside
Substrates: best substrate
Products: -
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UDP-glucuronate + chrysin

UDP + chrysin beta-D-glucuronide
Substrates: isozyme UGT1A9
Products: -
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UDP-glucuronate + chrysin
UDP + chrysin beta-D-glucuronide
Substrates: isozyme UGT1A7
Products: -
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UDP-glucuronate + chrysin
UDP + chrysin beta-D-glucuronide
Substrates: isozyme UGT1A8
Products: -
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UDP-glucuronate + chrysin
UDP + chrysin beta-D-glucuronide
Substrates: isozyme UGT1A1
Products: -
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UDP-glucuronate + chrysin
UDP + chrysin beta-D-glucuronide
Substrates: isozymes UGT1A1, UGT1A7, UGT1A8, UGT1A9, and UGT1A10
Products: -
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UDP-glucuronate + curcumin

UDP + curcumin beta-D-glucuronide
Substrates: isozyme UGT1A7
Products: -
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UDP-glucuronate + curcumin
UDP + curcumin beta-D-glucuronide
Substrates: isozyme UGT1A8
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UDP-glucuronate + curcumin
UDP + curcumin beta-D-glucuronide
Substrates: isozyme UGT1A1
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UDP-glucuronate + curcumin
UDP + curcumin beta-D-glucuronide
Substrates: isozymes UGT1A1, UGT1A7, UGT1A8, and UGT1A10
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UDP-glucuronate + desmethylnaproxen

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Substrates: UGT2B7 forms only the acyl glucuronide
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UDP-glucuronate + desmethylnaproxen
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Substrates: UGT1A1 catalyzes both the phenolic and acyl glucuronidation of desmethylnaproxen
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UDP-glucuronate + desmethylnaproxen
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Substrates: UGT 1A3 forms only the acyl glucuronide
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UDP-glucuronate + desmethylnaproxen
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Substrates: UGT 1A6 forms only the acyl glucuronide
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UDP-glucuronate + desmethylnaproxen
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Substrates: UGT1A7 catalyzes both the phenolic and acyl glucuronidation of desmethylnaproxen UGT 1A6 forms only the acyl glucuronide
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UDP-glucuronate + desmethylnaproxen
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Substrates: UGT1A9 catalyzes both the phenolic and acyl glucuronidation of desmethylnaproxen UGT 1A6 forms only the acyl glucuronide
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UDP-glucuronate + diclofenac

UDP + diclofenac beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
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UDP-glucuronate + diclofenac
UDP + diclofenac beta-D-glucuronoside
Substrates: very low activity
Products: -
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UDP-glucuronate + diclofenac
UDP + diclofenac beta-D-glucuronoside
Substrates: low activity
Products: -
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UDP-glucuronate + diclofenac
UDP + diclofenac beta-D-glucuronoside
Substrates: high activity
Products: -
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UDP-glucuronate + diphenhydramine

UDP + diphenhydramine beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
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UDP-glucuronate + diphenhydramine
UDP + diphenhydramine beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + entacapone

UDP + entacapone beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + entacapone
UDP + entacapone beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + entacapone
UDP + entacapone beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + entacapone

UDP + entacapone beta-D-glucuronoside
Substrates: very low activity
Products: -
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UDP-glucuronate + entacapone
UDP + entacapone beta-D-glucuronoside
Substrates: low activity
Products: -
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UDP-glucuronate + entacapone
UDP + entacapone beta-D-glucuronoside
Substrates: very high activity
Products: -
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UDP-glucuronate + entacapone
UDP + entacapone beta-D-glucuronoside
Substrates: high activity
Products: -
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UDP-glucuronate + estradiol

UDP + estradiol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: the enzyme UGT1A9 is active with estrogens
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UDP-glucuronate + estradiol
UDP + estradiol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
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UDP-glucuronate + ethanol

UDP + ethyl beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + ethanol
UDP + ethyl beta-D-glucuronoside
Substrates: high activity
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UDP-glucuronate + ethanol
UDP + ethyl beta-D-glucuronoside
Substrates: highest activity with enzymes UGT1A9 and UGT2B7
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UDP-glucuronate + ethinylestradiol

UDP + ethinylestradiol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
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UDP-glucuronate + ethinylestradiol
UDP + ethinylestradiol beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + ethinylestradiol
UDP + ethinylestradiol beta-D-glucuronoside
Substrates: very low activity
Products: -
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UDP-glucuronate + eugenol

UDP + eugenol beta-D-glucuronide
Substrates: isozyme UGT1A7
Products: -
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UDP-glucuronate + eugenol
UDP + eugenol beta-D-glucuronide
Substrates: isozymes UGT1A7, and UGT1A10
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UDP-glucuronate + genistein

UDP + genistein beta-D-glucuronide
Substrates: isozyme UGT1A7
Products: -
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UDP-glucuronate + genistein
UDP + genistein beta-D-glucuronide
Substrates: isozyme UGT1A1
Products: -
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UDP-glucuronate + genistein
UDP + genistein beta-D-glucuronide
Substrates: isozymes UGT1A1, UGT1A7, and UGT1A10
Products: -
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UDP-glucuronate + grepafloxacin

UDP + grepafloxacin beta-D-glucuronide
Substrates: low activity with isozyme UGT1A1
Products: -
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UDP-glucuronate + grepafloxacin
UDP + grepafloxacin beta-D-glucuronide
Substrates: low activity with isozyme UGT1A3
Products: -
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UDP-glucuronate + grepafloxacin
UDP + grepafloxacin beta-D-glucuronide
Substrates: -
Products: -
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UDP-glucuronate + grepafloxacin
UDP + grepafloxacin beta-D-glucuronide
Substrates: high activity with isozyme UGT1A9
Products: -
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UDP-glucuronate + imipramine

UDP + imipramine beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
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UDP-glucuronate + imipramine
UDP + imipramine beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + indomethacin

UDP + indomethacin beta-D-glucuronoside
Substrates: very low activity
Products: -
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UDP-glucuronate + indomethacin
UDP + indomethacin beta-D-glucuronoside
Substrates: low activity
Products: -
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UDP-glucuronate + indomethacin
UDP + indomethacin beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + indomethacin
UDP + indomethacin beta-D-glucuronoside
Substrates: high activity
Products: -
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UDP-glucuronate + L-thyroxine

UDP + L-thyroxyl beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: UGT1A1 and UGT1A3 are the major UGTs glucuronidating T4 at the hydroxyl and carboxyl groups, respectively
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UDP-glucuronate + L-thyroxine
UDP + L-thyroxyl beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
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UDP-glucuronate + levofloxacin

UDP + levofloxacin beta-D-glucuronide
Substrates: high activity with isozyme UGT1A1
Products: -
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UDP-glucuronate + levofloxacin
UDP + levofloxacin beta-D-glucuronide
Substrates: high activity with isozyme UGT1A3
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UDP-glucuronate + levofloxacin
UDP + levofloxacin beta-D-glucuronide
Substrates: high activity with isozyme UGT1A7
Products: -
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UDP-glucuronate + levofloxacin
UDP + levofloxacin beta-D-glucuronide
Substrates: high activity with isozyme UGT1A9
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UDP-glucuronate + levomedetomidine

UDP + levomedetomidine beta-D-glucuronoside
Substrates: low activity
Products: -
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UDP-glucuronate + levomedetomidine
UDP + levomedetomidine beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + morphine

UDP + morphine 3-beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + morphine
UDP + morphine 3-beta-D-glucuronoside
Substrates: morphine-3-glucuronidation is a marker of conjugation by human UGT2B7
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UDP-glucuronate + morphine

UDP + morphine-3-beta-D-glucuronide
Substrates: regioselectivity of activity is altered by cytochrome P450 enzyme CYP3A4 so that the ratio of morphine activation/detoxification is increased
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UDP-glucuronate + morphine
UDP + morphine-3-beta-D-glucuronide
Substrates: regioselective
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UDP-glucuronate + morphine
UDP + morphine-3-beta-D-glucuronide
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Substrates: isozymes UGT1A1, UGT1A3, UGT1A6, UGT1A8, UGT1A9, UGT1A10, and UGT2B7
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UDP-glucuronate + morphine
UDP + morphine-3-beta-D-glucuronide
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Substrates: isozyme UGT2B7, low activity with isozymes UGT1A3, UGT1A10, UGT2B4 and UGT1A9
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UDP-glucuronate + morphine
UDP + morphine-3-beta-D-glucuronide
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Substrates: isozyme UGT1A1
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UDP-glucuronate + morphine
UDP + morphine-3-beta-D-glucuronide
Substrates: -
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UDP-glucuronate + morphine

UDP + morphine-6-beta-D-glucuronide
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Substrates: isozyme UGT2B7
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UDP-glucuronate + morphine
UDP + morphine-6-beta-D-glucuronide
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Substrates: isozymes UGT2B4 and UGT2B7, low activity with isozymes UGT1A1, and UGT1A3
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UDP-glucuronate + morphine
UDP + morphine-6-beta-D-glucuronide
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Substrates: isozyme UGT1A1
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UDP-glucuronate + morphine
UDP + morphine-6-beta-D-glucuronide
Substrates: -
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UDP-glucuronate + moxifloxacin

UDP + moxifloxacin beta-D-glucuronide
Substrates: high activity with isozyme UGT1A1
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UDP-glucuronate + moxifloxacin
UDP + moxifloxacin beta-D-glucuronide
Substrates: very low activity with isozyme UGT1A3
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UDP-glucuronate + moxifloxacin
UDP + moxifloxacin beta-D-glucuronide
Substrates: low activity with isozyme UGT1A7
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UDP-glucuronate + moxifloxacin
UDP + moxifloxacin beta-D-glucuronide
Substrates: low activity with isozyme UGT1A9
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UDP-glucuronate + mycophenolic acid

UDP + mycophenolic acid-acyl-glucuronide
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Substrates: mycophenolic acid is the active metabolite of immunosuppressant mycophenolate mofetil
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UDP-glucuronate + mycophenolic acid
UDP + mycophenolic acid-acyl-glucuronide
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Substrates: isozymes UGT1A9 and UGT2B7
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UDP-glucuronate + mycophenolic acid

UDP + mycophenolic acid-phenyl-glucuronide
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Substrates: mycophenolic acid is the active metabolite of immunosuppressant mycophenolate mofetil
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UDP-glucuronate + mycophenolic acid
UDP + mycophenolic acid-phenyl-glucuronide
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Substrates: isozymes UGT1A9 and UGT2B7
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UDP-glucuronate + naproxen

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Substrates: UGT2B7 is responsible for human hepatic naproxen acyl glucuronidation, which is the primary elimination pathway for this drug
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UDP-glucuronate + naproxen
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Substrates: -
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UDP-glucuronate + naringenin

UDP + naringenin beta-D-glucuronide
Substrates: isozyme UGT1A7
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UDP-glucuronate + naringenin
UDP + naringenin beta-D-glucuronide
Substrates: isozyme UGT1A1
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UDP-glucuronate + naringenin
UDP + naringenin beta-D-glucuronide
Substrates: isozymes UGT1A1, UGT1A7, and UGT1A10
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UDP-glucuronate + olanzapine

UDP + olanzapine beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
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UDP-glucuronate + olanzapine
UDP + olanzapine beta-D-glucuronoside
Substrates: -
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UDP-glucuronate + phloretin

UDP + phloretin beta-D-glucuronide
Substrates: isozyme UGT1A7
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UDP-glucuronate + phloretin
UDP + phloretin beta-D-glucuronide
Substrates: isozyme UGT1A8
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UDP-glucuronate + phloretin
UDP + phloretin beta-D-glucuronide
Substrates: isozymes UGT1A7, UGT1A8, and UGT1A10
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UDP-glucuronate + propofol

UDP + propofol beta-D-glucuronide
Substrates: -
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UDP-glucuronate + propofol
UDP + propofol beta-D-glucuronide
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Substrates: isozyme UGT1A9
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UDP-glucuronate + propofol
UDP + propofol beta-D-glucuronide
Substrates: -
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UDP-glucuronate + propofol

UDP + propofol beta-D-glucuronoside
Substrates: -
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UDP-glucuronate + propofol
UDP + propofol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
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UDP-glucuronate + propofol
UDP + propofol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
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UDP-glucuronate + propofol
UDP + propofol beta-D-glucuronoside
Substrates: -
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UDP-glucuronate + quercetin

UDP + quercetin beta-D-glucuronide
Substrates: isozyme UGT1A7
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UDP-glucuronate + quercetin
UDP + quercetin beta-D-glucuronide
Substrates: isozyme UGT1A1
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UDP-glucuronate + quercetin
UDP + quercetin beta-D-glucuronide
Substrates: isozymes UGT1A1, UGT1A7, and UGT1A10
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UDP-glucuronate + quinazarin

UDP + quinazarin beta-D-glucuronide
Substrates: isozyme UGT1A7
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UDP-glucuronate + quinazarin
UDP + quinazarin beta-D-glucuronide
Substrates: isozyme UGT1A1
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UDP-glucuronate + quinazarin
UDP + quinazarin beta-D-glucuronide
Substrates: isozymes UGT1A1, UGT1A7, and UGT1A10
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UDP-glucuronate + serotonin

UDP + serotonin beta-D-glucuronide
Substrates: -
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UDP-glucuronate + serotonin
UDP + serotonin beta-D-glucuronide
Substrates: in vitro substrate, isozyme UGT1A6
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UDP-glucuronate + serotonin

UDP + serotonin beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: mucosal serotonin and its metabolite 5-hydroxytryptophol are solely conjugated by UGT1A6
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UDP-glucuronate + serotonin
UDP + serotonin beta-D-glucuronoside
Substrates: -
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UDP-glucuronate + sitafloxacin

UDP + sitafloxacin beta-D-glucuronide
Substrates: high activity with isozyme UGT1A1
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UDP-glucuronate + sitafloxacin
UDP + sitafloxacin beta-D-glucuronide
Substrates: low activity with isozyme UGT1A3
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UDP-glucuronate + sitafloxacin
UDP + sitafloxacin beta-D-glucuronide
Substrates: low activity with isozyme UGT1A7
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UDP-glucuronate + sitafloxacin
UDP + sitafloxacin beta-D-glucuronide
Substrates: high activity with isozyme UGT1A9
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UDP-glucuronate + tamoxifen

UDP + tamoxifen beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
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UDP-glucuronate + tamoxifen
UDP + tamoxifen beta-D-glucuronoside
Substrates: -
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UDP-glucuronate + testosterone

UDP + testosterone beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
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UDP-glucuronate + testosterone
UDP + testosterone beta-D-glucuronoside
Substrates: -
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UDP-glucuronate + thymol

UDP + thymol beta-D-glucuronide
Substrates: isozyme UGT1A7
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UDP-glucuronate + thymol
UDP + thymol beta-D-glucuronide
Substrates: isozymes UGT1A7, and UGT1A10
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UDP-glucuronate + umbelliferone

UDP + umbelliferone beta-D-glucuronide
Substrates: -
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UDP-glucuronate + umbelliferone
UDP + umbelliferone beta-D-glucuronide
Substrates: -
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UDP-glucuronate + zidovudine

UDP + zidovudine beta-D-glucuronoside
Substrates: -
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UDP-glucuronate + zidovudine
UDP + zidovudine beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
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UDP-glucuronate + zidovudine
UDP + zidovudine beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, O75310, P06133, P36537, P35504, Q6UWM9, Q9Y4X1, Q9BY64 Substrates: -
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ursodeoxycholic acid + UDPglucuronate

UDP + ursodeoxycholic acid O-glucuronide
-
Substrates: -
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ursodeoxycholic acid + UDPglucuronate
UDP + ursodeoxycholic acid O-glucuronide
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Substrates: highest activity among five bile acids studied
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valproic acid + UDPglucuronate

UDP + ?
-
Substrates: -
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valproic acid + UDPglucuronate
UDP + ?
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Substrates: glucuronidated by UGT2B7
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xanthotoxol + UDP-glucuronate

UDP + xanthotoxol 8-O-glucuronide
Substrates: isoform UGT2B7 is mainly responsible for xanthotoxol glucuronidation in the human liver
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xanthotoxol + UDP-glucuronate
UDP + xanthotoxol 8-O-glucuronide
Substrates: isoform UGT1A10 is mainly responsible for xanthotoxol glucuronidation in the human small intestine
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xanthotoxol + UDP-glucuronate
UDP + xanthotoxol 8-O-glucuronide
Substrates: -
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xanthotoxol + UDP-glucuronate
UDP + xanthotoxol 8-O-glucuronide
Substrates: isoform UGT1A1 is mainly responsible for xanthotoxol glucuronidation in the human liver
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additional information

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Substrates: Xenobiotic glucuronidation summarized
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additional information
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Substrates: 36 substrates for HGT2B7H and HGT2B7Y. HGT2B7 glucuronidates both hydroxyl and carboxyl functions of bile acids, retinols and hydroxylated fatty acids
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additional information
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Substrates: 36 substrates for HGT2B7H and HGT2B7Y. HGT2B7 glucuronidates both hydroxyl and carboxyl functions of bile acids, retinols and hydroxylated fatty acids
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additional information
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Substrates: 36 substrates for HGT2B7H and HGT2B7Y. HGT2B7 glucuronidates both hydroxyl and carboxyl functions of bile acids, retinols and hydroxylated fatty acids
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additional information
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Substrates: 36 substrates for HGT2B7H and HGT2B7Y. HGT2B7 glucuronidates both hydroxyl and carboxyl functions of bile acids, retinols and hydroxylated fatty acids
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additional information
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Substrates: 36 substrates for HGT2B7H and HGT2B7Y. HGT2B7 glucuronidates both hydroxyl and carboxyl functions of bile acids, retinols and hydroxylated fatty acids
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additional information
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Substrates: 36 substrates for HGT2B7H and HGT2B7Y. HGT2B7 glucuronidates both hydroxyl and carboxyl functions of bile acids, retinols and hydroxylated fatty acids
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additional information
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Substrates: 36 substrates for HGT2B7H and HGT2B7Y. HGT2B7 glucuronidates both hydroxyl and carboxyl functions of bile acids, retinols and hydroxylated fatty acids
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additional information
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Substrates: simple planar phenols, anthraquinones and opioid compounds glucuronidated by UGT1.1, aliphatic and monoterpenoid alcohols and amines not glucuronidated
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additional information
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Substrates: UGT1A3 inactive towards 4-hydroxyestrone and 16 alpha-hydroxyestrone
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additional information
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Substrates: specificity of cloned human isozymes
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additional information
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Substrates: no activity with androsterone, 5alpha-androstane-3alpha,17beta-diol
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additional information
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Substrates: affinity of unconjugated bile acids decrease with increasing number of hydroxyl groups in the bile acid skeleton
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additional information
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Substrates: wide variety of endogenous steroidal hormones, bile acids, retinoids and tyroid hormones glucuronidated by isozymes of UGT1A family
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additional information
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Substrates: elimination of lipid-soluble endogenous compounds and xenobiotics
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additional information
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Substrates: elimination of lipid-soluble endogenous compounds and xenobiotics
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additional information
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Substrates: elimination of lipid-soluble endogenous compounds and xenobiotics
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additional information
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Substrates: steroid hormones, bile acids, all trans retinoic acids and fatty acids glucuronidated by isozymes of UGTB2 family
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additional information
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Substrates: certain endogenous estrogens glucuronidated by UGT1.1 at 3-hydroxyl group of the A ring of steroids
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additional information
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Substrates: isozyme UGT2B7 is involved in metabolism of mineralocorticoid and glucocorticoid hormones, two-cell mechanism of aldosterone action and metabolism in the kidney
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additional information
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Substrates: isozyme UGT2B7 is involved in metabolism of mineralocorticoid and glucocorticoid hormones, two-cell mechanism of aldosterone action and metabolism in the kidney
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additional information
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Substrates: isozymes are involved in detoxification of metabolites, drugs, toxins, and environmental chemicals via conjugation to glucuronic acid, physiological roles and overlapping activities
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additional information
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Substrates: isozymes are involved in detoxification of metabolites, drugs, toxins, and environmental chemicals via conjugation to glucuronic acid, physiological roles and overlapping activities
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additional information
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Substrates: isozymes are involved in detoxification of metabolites, drugs, toxins, and environmental chemicals via conjugation to glucuronic acid, physiological roles and overlapping activities
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additional information
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Substrates: isozymes are involved in detoxification of metabolites, drugs, toxins, and environmental chemicals via conjugation to glucuronic acid, physiological roles and overlapping activities
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additional information
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Substrates: isozymes are involved in detoxification of metabolites, drugs, toxins, and environmental chemicals via conjugation to glucuronic acid, physiological roles and overlapping activities
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additional information
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Substrates: enzyme are involved in biosynthesis of HNK-1 carbohydrate
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Substrates: isozymes facilitate the excretion of estrogens to glucuronides, the most abundant estrogen conjugates
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Substrates: the enzyme is involved acyl glucuronidation, an important metabolic pathway for fluoroquinolone antobiotics
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Substrates: the enzyme is involved acyl glucuronidation, an important metabolic pathway for fluoroquinolone antobiotics
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additional information
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Substrates: the enzyme is involved acyl glucuronidation, an important metabolic pathway for fluoroquinolone antobiotics
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additional information
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Substrates: the enzyme is involved acyl glucuronidation, an important metabolic pathway for fluoroquinolone antobiotics
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additional information
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Substrates: the enzyme is involved acyl glucuronidation, an important metabolic pathway for fluoroquinolone antobiotics
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additional information
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Substrates: enzyme UGT2B7 plays a crucial role in drug detoxificiation
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Substrates: isozyme UGT2B7 is the major isozyme involved in metabolization of morphine in the liver
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Substrates: isozyme UGT2B7 is involved in glucuronidation of a wide array of clinically important drugs and endogenous compounds in humans
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Substrates: substrate specificities of isozymes, overview
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Substrates: substrate specificities of isozymes, overview
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additional information
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Substrates: substrate specificities of isozymes, overview
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additional information
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Substrates: substrate specificities of isozymes, overview
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additional information
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Substrates: substrate specificities of isozymes, overview
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additional information
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Substrates: the recombinant GlcAT-P is highly specific for terminal type II structure, Galbeta1-4GlcNAc, while the recombinant GlcAT-S recognizes type I, Galbeta1-3GlcNAc, and type II structures
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additional information
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Substrates: substrate specificities of wild-type and recombinant soluble mutant isozyme UGT1A9
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additional information
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Substrates: substrate specificities of wild-type and recombinant soluble mutant isozyme UGT1A9
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additional information
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Substrates: UGT2B7 interacts with CYP3A4, the latter reduces UGT2B7 activity in detergent n-octylglucoside treated recombinant COS-cell microsomes
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Substrates: UGT2B7 interacts with CYP3A4, the latter reduces UGT2B7 activity in detergent n-octylglucoside treated recombinant COS-cell microsomes
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Substrates: substrate specificity of isozymes, overview
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Substrates: substrate specificity of isozymes, overview
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additional information
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Substrates: substrate specificity of isozymes, overview
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Substrates: substrate specificity of isozymes, overview
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additional information
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Substrates: substrate specificity of isozymes, overview
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additional information
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Substrates: substrate specificity of isozymes, overview
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additional information
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Substrates: substrate specificty of isozymes of the 1A subfamily
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Substrates: substrate specificty of isozymes of the 1A subfamily
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Substrates: substrate specificty of isozymes of the 1A subfamily
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Substrates: substrate specificty of isozymes of the 1A subfamily
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Substrates: substrate specificty of isozymes of the 1A subfamily
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Substrates: substrate specificity, no substrates are lorazepam, lithocholic acid, furosemide, propofol, ethinylestradiol, and testosterone
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Substrates: the UGT2B7*2 polymorphism is not a determinant of glucuronodation specificity, substrate specificity by isozyme UGT2B7, overview
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additional information
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Substrates: in contrast to isozymes UGT1A1 and UGT1A7, the isozyme UGT1A9 does not show polymorphism influencing the glucuronidation activity of SN-38
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Substrates: in contrast to isozymes UGT1A1 and UGT1A7, the isozyme UGT1A9 does not show polymorphism influencing the glucuronidation activity of SN-38
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Substrates: substrate specificities of different isozymes
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Substrates: glucuronidation by the UDP glucuronosyltransferase 1A enzymes is a major pathway for elimination of drugs and endogenous substances, such as bilirubin
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Substrates: direct inhibition of UGT1A1-mediated bilirubin glucuronidation may provide a mechanism for the reversible hyperbilirubinemia associated with administration of atazanavir as well as indinavir
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Substrates: no activity with p-ethoxyphenylurea
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Substrates: no activity with p-ethoxyphenylurea
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Substrates: no activity with p-ethoxyphenylurea
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additional information
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Substrates: no activity with p-ethoxyphenylurea
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additional information
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Substrates: no activity with p-ethoxyphenylurea
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Substrates: no activity with p-ethoxyphenylurea
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Substrates: no activity with p-ethoxyphenylurea
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Substrates: general chemical properties, such as chemical size, shape, flexibility, and hydrophobicity, may be of secondary importance to the steric and electronic character immediately local to the nucleophilic atom. Molecular recognition based on the local structure is likely to be important for the ability of UGT to detoxify chemicals that differ greatly in gross molecular structure
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Substrates: no glucuronidation of 4-aminobiphenyl, a good substrate for the highly homologous enzymes UGT1A4 and UGT1A3
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additional information
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Substrates: no glucuronidation of 4-aminobiphenyl, a good substrate for the highly homologous enzymes UGT1A4 and UGT1A3
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Substrates: isozyme UGT2B15 is a critical enzyme for the local inactivation of androgens and major determinants of the androgen response in prostate cancer LNCaP cells, overview
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Substrates: isozyme UGT2B15 is a critical enzyme for the local inactivation of androgens and major determinants of the androgen response in prostate cancer LNCaP cells, overview
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Substrates: isozyme UGT2B15 is a critical enzyme for the local inactivation of androgens and major determinants of the androgen response in prostate cancer LNCaP cells, overview
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Substrates: The phenolic glucuronidation of the curcuminoids is predominantly catalyzed by hepatic isozyme UGT1A1 and intestinal isozymes UGT1A8 and UGT1A10, whereas isozymes UGT1A9, UGT2B7, and UGT1A8 exhibit high activities for hexahydro-curcuminoids, substrate specificities of recombinant isozymes in insect cell microsomes, overview
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Substrates: UGTs play an important role in the defense against potentially hazardous xenobiotics, and they participate in the metabolism and homeostasis of many endogenous compounds, including bilirubin and steroid hormones, overview
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Substrates: UGTs play an important role in the defense against potentially hazardous xenobiotics, and they participate in the metabolism and homeostasis of many endogenous compounds, including bilirubin and steroid hormones, overview
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Substrates: UGTs play an important role in the defense against potentially hazardous xenobiotics, and they participate in the metabolism and homeostasis of many endogenous compounds, including bilirubin and steroid hormones, overview
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Substrates: UGTs play an important role in the defense against potentially hazardous xenobiotics, and they participate in the metabolism and homeostasis of many endogenous compounds, including bilirubin and steroid hormones, overview
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Substrates: the role of UGT enzymes in the liver is recognized as a highly efficient and constitutive mechanism of detoxification of endogenous and exogenous compounds, particularly for steroid hormones, metabolism of adrenal and testicular steroid hormones, overview
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Substrates: the role of UGT enzymes in the liver is recognized as a highly efficient and constitutive mechanism of detoxification of endogenous and exogenous compounds, particularly for steroid hormones, metabolism of adrenal and testicular steroid hormones, overview
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Substrates: the role of UGT enzymes in the liver is recognized as a highly efficient and constitutive mechanism of detoxification of endogenous and exogenous compounds, particularly for steroid hormones, metabolism of adrenal and testicular steroid hormones, overview
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Substrates: regulation of isozyme UGT1A1 by progesterone and its impact on labetalol elimination, overview
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Substrates: regulation of isozyme UGT1A1 by progesterone and its impact on labetalol elimination, overview
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Substrates: regulation of isozyme UGT1A1 by progesterone and its impact on labetalol elimination, overview
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Substrates: regulation of isozyme UGT1A1 by progesterone and its impact on labetalol elimination, overview
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Substrates: regulation of isozyme UGT1A1 by progesterone and its impact on labetalol elimination, overview
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Substrates: regulation of isozyme UGT1A1 by progesterone and its impact on labetalol elimination, overview
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Substrates: regulation of isozyme UGT1A1 by progesterone and its impact on labetalol elimination, overview
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the enzyme is involved in clearance and detoxification of many chemical compounds, overview
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Substrates: isozyme UGT2B17 is a critical enzyme for the local inactivation of androgens and major determinants of the androgen response in prostate cancer LNCaP cells, overview
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Substrates: isozyme UGT2B17 is a critical enzyme for the local inactivation of androgens and major determinants of the androgen response in prostate cancer LNCaP cells, overview
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Substrates: isozyme UGT2B17 is a critical enzyme for the local inactivation of androgens and major determinants of the androgen response in prostate cancer LNCaP cells, overview
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Substrates: key amino acid residues responsible for the differences in substrate specificity of isozymes UGT1A9 and UGT1A8, overview
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Substrates: key amino acid residues responsible for the differences in substrate specificity of isozymes UGT1A9 and UGT1A8, overview
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Substrates: key amino acid residues responsible for the differences in substrate specificity of isozymes UGT1A9 and UGT1A8, overview
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Substrates: key amino acid residues responsible for the differences in substrate specificity of isozymes UGT1A9 and UGT1A8, overview
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Substrates: key amino acid residues responsible for the differences in substrate specificity of isozymes UGT1A9 and UGT1A8, overview
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Substrates: ten flavonoid aglycons are used as substrates, spanning the subclasses of flavones, flavonols, and flavanones. The products are characterized by LC-MS and LC-MSn, with post-column cobalt complexation employed to pinpoint the specific sites of conjugation. The dissociation of complexes of the form [Co(II) (flavonoid glucuronide-H) (4,7-diphenyl-1,10-phenanthroline)2]+ allow identification of the products and differentiation of isomers. The correlation between glycosylation site and elution order is used to provide additional structural confirmation. Flavonoids lacking a 3' hydroxyl group are glucuronidated only at position 7, while those containing this functionality also form 3'-O-glucuronides and sometimes 4'-O-glucuronides, thus supporting the conclusion that the presence or absence of the 3'-OH group is the major determinant of the regioselectivity of glucuronidation. Moreover, the specific distribution of multiple glucuronide products, 7-O, 3'-O, 4'-O, is governed by the subclass of flavonoid, structure-activity relationships, overview
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Substrates: kinetic modeling of the interactions between 4-methylumbelliferone, 1-naphthol, and zidovudine glucuronidation by UGT2B7 provides evidence for multiple substrate binding and effector sites, overview
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Substrates: substrate concentration-rate profiles of 25-O-glucuronide formation by UGT1A4, UGT2B4, and UGT2B7, overview
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Substrates: substrate concentration-rate profiles of 25-O-glucuronide formation by UGT1A4, UGT2B4, and UGT2B7, overview
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Substrates: substrate specificity of isozyme UGT2B15, overview
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Substrates: substrate specificity of isozyme UGT2B15, overview
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Substrates: substrate specificity of isozyme UGT2B15, overview
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Substrates: regiospecific glucuronidation of sartans by different isozymes, overview
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Substrates: determination of UDP-glucuronate binding sites in isozymes UGT1A10 and UGT1A7 using inhibitor binding and peptide mapping, overview
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Substrates: detailed structure-activity relationships with respect to functionality, stereochemical properties, and steric features, with 3D-quantitative structure-activity relationship using comparative molecular similarity analysis, overview. The glucuronidation of substrate compounds is prevented by the introduction of bulky substituents such as isopropyl, tert-butyl, and phenyl groups, overview
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Substrates: substrate specificity of UGT isozymes with morphine, overview, no or poor activity with isozymes UGT1A3, UGT1A4, UGT1A6, UGT1A7, UGT1A9, UGT1A10, UGT2B15, and UGT2B17
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Substrates: substrate specificity of UGT isozymes with morphine, overview, no or poor activity with isozymes UGT1A3, UGT1A4, UGT1A6, UGT1A7, UGT1A9, UGT1A10, UGT2B15, and UGT2B17
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Substrates: regioselectivity of recombinant isozymes and liver microsomes, overview
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Substrates: regioselectivity of recombinant isozymes and liver microsomes, overview
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Substrates: UGT1A1 substrate specificity, overview
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Substrates: UGT1A1 substrate specificity, overview
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Substrates: UGT1A1 substrate specificity, overview
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Substrates: UGT1A1 substrate specificity, overview
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Substrates: UGT1A1 substrate specificity, overview
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Substrates: specific phospho-groups in UGT1A7 determine substrate selections, suggests regulated phosphorylation allows adaptations regarding differential phosphate utilization by UGTs to function efficiently
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Substrates: substrate specificity, UGT1A8, UGT1A4, UGT1A6, UGT1A7, and UGT2B7 do not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: substrate specificity, UGT1A8, UGT1A4, UGT1A6, UGT1A7, and UGT2B7 do not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: substrate specificity, UGT1A8, UGT1A4, UGT1A6, UGT1A7, and UGT2B7 do not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: substrate specificity, UGT1A8, UGT1A4, UGT1A6, UGT1A7, and UGT2B7 do not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: no activity of UGT2A3 with 4-nitrophenol, 4-methylumbelliferone, or any other small phenolic substrate
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Substrates: no activity of UGT2A3 with 4-nitrophenol, 4-methylumbelliferone, or any other small phenolic substrate
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Substrates: prediction of substrates for several isozymes by two dimensional-QSAR modelling, regioselective glucuronidation of isozymes, overview, substrate recognition, and multiple pharmacophore perception, overview
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Substrates: isozyme UGT1A8 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT1A8 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT1A8 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT1A8 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT1A8 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT1A8 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT1A8 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT1A8 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT1A10 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT1A10 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT1A10 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT1A10 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT1A10 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT1A10 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT1A10 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT1A10 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT2B7 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT2B7 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT2B7 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT2B7 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT2B7 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT2B7 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT2B7 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: isozyme UGT2B7 exhibits high overall glucuronidating activities compared to other UGT isozymes
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Substrates: no activity by isozyme UGT2B15 with trans-4-hydroxytamoxifen
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Substrates: no activity by isozyme UGT2B15 with trans-4-hydroxytamoxifen
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Substrates: no activity by isozyme UGT2B15 with trans-4-hydroxytamoxifen
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Substrates: no activity by isozyme UGT2B15 with trans-4-hydroxytamoxifen
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Substrates: no activity by isozyme UGT2B15 with trans-4-hydroxytamoxifen
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Substrates: no activity by isozyme UGT2B15 with trans-4-hydroxytamoxifen
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Substrates: no activity by isozyme UGT2B15 with trans-4-hydroxytamoxifen
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Substrates: no activity by isozyme UGT2B15 with trans-4-hydroxytamoxifen
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Substrates: substrate specificity of isozyme UGT2B7, overview
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Substrates: substrate specificity of isozyme UGT2B7, overview
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Substrates: substrate specificity of isozyme UGT2B7, overview
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Substrates: substrate specificity, UGT1A9 does not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: substrate specificity, UGT1A9 does not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: substrate specificity, UGT1A9 does not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: substrate specificity, UGT1A9 does not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: substrate specificity, UGT1A1 does not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: substrate specificity, UGT1A1 does not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: substrate specificity, UGT1A1 does not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: substrate specificity, UGT1A1 does not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: inhibitor beta-phenyllongifolol is not glucuronidated by UGT2B7 or other hepatic UGTs
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Substrates: inhibitor beta-phenyllongifolol is not glucuronidated by UGT2B7 or other hepatic UGTs
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Substrates: substrate specificity, UGT1A10 does not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: substrate specificity, UGT1A10 does not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: substrate specificity, UGT1A10 does not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: substrate specificity, UGT1A10 does not show activity with with (R)- and (S)-warfarin, racemic warfarin, or 10-hydroxywarfarin, overview
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Substrates: isozymes UGT1A10, UGT1A8, and UGT2B7 exhibit the highest overall glucuronidating activities of the UGT isozymes
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Substrates: isozymes UGT1A10, UGT1A8, and UGT2B7 exhibit the highest overall glucuronidating activities of the UGT isozymes
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Substrates: isozymes UGT1A10, UGT1A8, and UGT2B7 exhibit the highest overall glucuronidating activities of the UGT isozymes
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Substrates: isozymes UGT1A10, UGT1A8, and UGT2B7 exhibit the highest overall glucuronidating activities of the UGT isozymes
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Substrates: isozymes UGT1A10, UGT1A8, and UGT2B7 exhibit the highest overall glucuronidating activities of the UGT isozymes
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Substrates: isozymes UGT1A10, UGT1A8, and UGT2B7 exhibit the highest overall glucuronidating activities of the UGT isozymes
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Substrates: isozymes UGT1A10, UGT1A8, and UGT2B7 exhibit the highest overall glucuronidating activities of the UGT isozymes
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Substrates: isozymes UGT1A10, UGT1A8, and UGT2B7 exhibit the highest overall glucuronidating activities of the UGT isozymes
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Substrates: no substrate of isoform UGT1A8: 4-nitrophenol
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Substrates: no substrate of isoform UGT1A8: 4-nitrophenol
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Substrates: no substrate of isoform UGT1A8: 4-nitrophenol
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Substrates: no substrate of isoform UGT1A8: 4-nitrophenol
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Substrates: no substrate of isoform UGT1A8: 4-nitrophenol
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Substrates: the orientation of the substrate correlates with the conjugation capacity in in vitro experiments. As glucuronidation is an intermolecular rearrangement reaction, the conjugation reaction proceeds only when the hydroxyl group of the substrate is oriented towards the coenzyme, which allows the proton transfer to occur
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Substrates: there are no significant differences in the levels of kinetic parameters for 7-hydroxy-4-trifluoromethylcoumarin, estradiol at 3-hydroxy position and 7-ethyl-10-hydroxycamptothecin glucuronidation between humans and cynomolgus monkeys in enzymes from liver microsomes and recombinant isoforms UGT1A1. 7-Hydroxy-4-trifluoromethylcoumarin and estradiol glucuronidation by human liver microsomes exhibits biphasic and sigmoidal kinetics, respectively. 7-Ethyl-10-hydroxycamptothecin glucuronidation by human liver microsomes exhibits autoactivation kinetics
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Substrates: there are no significant differences in the levels of kinetic parameters for 7-hydroxy-4-trifluoromethylcoumarin, estradiol at 3-hydroxy position and 7-ethyl-10-hydroxycamptothecin glucuronidation between humans and cynomolgus monkeys in enzymes from liver microsomes and recombinant isoforms UGT1A1. 7-Hydroxy-4-trifluoromethylcoumarin and estradiol glucuronidation by human liver microsomes exhibits biphasic and sigmoidal kinetics, respectively. 7-Ethyl-10-hydroxycamptothecin glucuronidation by human liver microsomes exhibits autoactivation kinetics
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Substrates: isoform UGT2A1 is not active with substrates that form N-glucuronides, such as 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol, nicotine, or N-hydroxy-2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine
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Substrates: the pattern of human UDP-glucuronosyltransferases of subfamily 2B that glucuronidate ent-17beta-estradiol, particularly 2B15 and 2B17, resembles the glucuronidation of 17alpha-estradiol rather than 17beta-estradiol. The UDP-glucuronosyltransferases of subfamilies 1A and 2A exhibit higher degree of regioselectivity than enantioselectivity in the conjugation of these estradiols, regardless of whether the activity is primarily toward the non-chiral site, 3-OH, or the 17-OH group
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Substrates: UGT1A4 is the main enzyme involved in the metabolism of all compounds tested except for fluconazole, which is mainly metabolized by UGT2B7, probably mediating its O-glucuronide metabolism. UGT1A3 is also involved in the metabolism of all imidazoles but not triazoles
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Substrates: no activity with (E)-4-(3,5-dimethoxystyryl)-2,6-dinitrophenol, i.e. DNR-1, glucuronide formation is verified by beta-glucuronidase hydrolysis and LC-MS/MS analysis
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Substrates: trans-Resveratrol has powerful antioxidant, anti-inflammatory, anticarcinogenic, and antiaging properties, but its use as a therapeutic agent is limited by its rapid metabolism into its conjugated forms by UDP-glucuronosyltransferases. The limited bioavailability of tRes can be improved by modifying its structure to create analogues which can be glucuronidated at a lower rate than tRes itself. Three synthetic stilbenoids ((E)-3-(3-hydroxy-4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)acrylic acid, (E)-2,4-dimethoxy-6-(4-methoxystyryl)benzaldehyde oxime, and (E)-4-(3,5-dimethoxystyryl)-2,6-dinitrophenol) are designed based on the structure of tRes and synthesized. UDP-glucuronosyltransferases recognize and glucuronidate trans-resveratrol at each of the 3 hydroxyl groups attached to its aromatic rings
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Substrates: the human UGTs of subfamily 2A, UGT2A1, 2A2, and 2A3, show bile acid-conjugating activity
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Substrates: the human UGTs of subfamily 2A, UGT2A1, 2A2, and 2A3, show bile acid-conjugating activity
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Q9Y4X1
Substrates: the human UGTs of subfamily 2A, UGT2A1, 2A2, and 2A3, show bile acid-conjugating activity
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
Products: -
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additional information
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
Products: -
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additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
Products: -
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additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
Products: -
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additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
Products: -
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additional information
?
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-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
Products: -
?
additional information
?
-
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
Products: -
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additional information
?
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-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
Products: -
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additional information
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Substrates: no activity with gingerols by enzyme UGT1A3
Products: -
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additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A3
Products: -
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additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A3
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A3
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A3
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A3
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A3
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A3
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A3
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A3
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A3
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A3
Products: -
?
additional information
?
-
-
Substrates: no activity with gingerols by enzyme UGT1A3
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A4
Products: -
?
additional information
?
-
-
Substrates: no activity with gingerols by enzyme UGT1A4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
?
additional information
?
-
-
Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
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additional information
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
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additional information
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
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additional information
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
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additional information
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
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additional information
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
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additional information
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
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additional information
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
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additional information
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
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additional information
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
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additional information
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
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additional information
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
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additional information
?
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
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additional information
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Substrates: morphine glucuronidation and glucosidation represent complementary metabolic pathways that are both catalyzed by UDP-glucuronosyltransferase 2B7. Glucuronidation is the dominant metabolic pathway because the binding affinity of UDP-glucuronic acid to UGT2B7 is higher than that of UDPglucose
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additional information
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Substrates: morphine glucuronidation and glucosidation represent complementary metabolic pathways that are both catalyzed by UDP-glucuronosyltransferase 2B7. Glucuronidation is the dominant metabolic pathway because the binding affinity of UDP-glucuronic acid to UGT2B7 is higher than that of UDPglucose
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additional information
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Substrates: the enzyme UGT2B4 is also active with bile acids
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additional information
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Substrates: the enzyme UGT2B4 is also active with bile acids
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additional information
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Substrates: the enzyme UGT2B4 is also active with bile acids
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additional information
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Substrates: the enzyme UGT2B4 is also active with bile acids
Products: -
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additional information
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Substrates: the enzyme UGT2B4 is also active with bile acids
Products: -
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additional information
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Substrates: the enzyme UGT2B4 is also active with bile acids
Products: -
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additional information
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Substrates: the enzyme UGT2B4 is also active with bile acids
Products: -
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additional information
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Substrates: the enzyme UGT2B4 is also active with bile acids
Products: -
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additional information
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Substrates: the enzyme UGT2B4 is also active with bile acids
Products: -
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additional information
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Substrates: the enzyme UGT2B4 is also active with bile acids
Products: -
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additional information
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Substrates: the enzyme UGT2B4 is also active with bile acids
Products: -
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additional information
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Substrates: the enzyme UGT2B4 is also active with bile acids
Products: -
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additional information
?
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Substrates: the enzyme UGT2B4 is also active with bile acids
Products: -
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additional information
?
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Substrates: the enzyme UGT2B4 is also active with bile acids
Products: -
?
additional information
?
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Substrates: the enzyme UGT2B4 is also active with bile acids
Products: -
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additional information
?
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Substrates: the enzyme UGT2B4 is also active with bile acids
Products: -
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additional information
?
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Substrates: the enzyme UGT2B4 is also active with bile acids
Products: -
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additional information
?
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Substrates: the enzyme UGT2B4 is also active with bile acids
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additional information
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Substrates: the enzyme UGT2B4 is also active with bile acids
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additional information
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Substrates: 3'-azido-3'-deoxythymidine-glucuronidation activity is low in the microminipig compared with humans, morphine-3-glucuronidation activity in the microminipig is higher than that in humans
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additional information
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Substrates: 3'-azido-3'-deoxythymidine-glucuronidation activity is low in the microminipig compared with humans, morphine-3-glucuronidation activity in the microminipig is higher than that in humans
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additional information
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Substrates: 3'-azido-3'-deoxythymidine-glucuronidation activity is low in the microminipig compared with humans, morphine-3-glucuronidation activity in the microminipig is higher than that in humans
Products: -
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additional information
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Substrates: 3'-azido-3'-deoxythymidine-glucuronidation activity is low in the microminipig compared with humans, morphine-3-glucuronidation activity in the microminipig is higher than that in humans
Products: -
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additional information
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Substrates: 3'-azido-3'-deoxythymidine-glucuronidation activity is low in the microminipig compared with humans, morphine-3-glucuronidation activity in the microminipig is higher than that in humans
Products: -
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additional information
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Substrates: 3'-azido-3'-deoxythymidine-glucuronidation activity is low in the microminipig compared with humans, morphine-3-glucuronidation activity in the microminipig is higher than that in humans
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additional information
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Substrates: most, if not all, UGT2B10 substrates are additionally glucuronidated by UGT1A4 and biphasic kinetics are frequently observed when human liver microsomes are used as the enzyme source. UGT2B10 is the high-affinity enzyme involved in most reactions. Thirteen recombinant human UGTs are screened for cotinine N-glucuronide formation, i.e. UGT 1A1, 1A3, 1A4, 1A6, 1A7, 1A8, 1A9, 1A10, 2B4, 2B7, 2B10, 2B15, and 2B17, cotinine is a highly selective substrate of human liver microsomal UGT2B10
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additional information
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Substrates: most, if not all, UGT2B10 substrates are additionally glucuronidated by UGT1A4 and biphasic kinetics are frequently observed when human liver microsomes are used as the enzyme source. UGT2B10 is the high-affinity enzyme involved in most reactions. Thirteen recombinant human UGTs are screened for cotinine N-glucuronide formation, i.e. UGT 1A1, 1A3, 1A4, 1A6, 1A7, 1A8, 1A9, 1A10, 2B4, 2B7, 2B10, 2B15, and 2B17, cotinine is a highly selective substrate of human liver microsomal UGT2B10
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additional information
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Substrates: no activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, entacapone, levomedetomidine, diclofenac, indomethacin, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
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additional information
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Substrates: no activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, entacapone, levomedetomidine, diclofenac, indomethacin, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
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additional information
?
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Substrates: no activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, entacapone, levomedetomidine, diclofenac, indomethacin, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
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additional information
?
-
Substrates: no activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, entacapone, levomedetomidine, diclofenac, indomethacin, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
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Substrates: no activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, entacapone, levomedetomidine, diclofenac, indomethacin, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
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additional information
?
-
Substrates: no activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, entacapone, levomedetomidine, diclofenac, indomethacin, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
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Substrates: no activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, entacapone, levomedetomidine, diclofenac, indomethacin, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, entacapone, levomedetomidine, diclofenac, indomethacin, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, entacapone, levomedetomidine, diclofenac, indomethacin, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
-
Substrates: no activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, entacapone, levomedetomidine, diclofenac, indomethacin, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
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additional information
?
-
Substrates: no activity with dexmedetomidine, levomedetomidine, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
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additional information
?
-
Substrates: no activity with dexmedetomidine, levomedetomidine, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
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additional information
?
-
Substrates: no activity with dexmedetomidine, levomedetomidine, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
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additional information
?
-
Substrates: no activity with dexmedetomidine, levomedetomidine, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with dexmedetomidine, levomedetomidine, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
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additional information
?
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Substrates: no activity with dexmedetomidine, levomedetomidine, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
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additional information
?
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Substrates: no activity with dexmedetomidine, levomedetomidine, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
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Substrates: no activity with dexmedetomidine, levomedetomidine, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
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additional information
?
-
Substrates: no activity with dexmedetomidine, levomedetomidine, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
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additional information
?
-
-
Substrates: no activity with dexmedetomidine, levomedetomidine, 4-methylumbelliferone, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no or poor activity with bilirubin, dexmedetomidine, diclofenac, levomedetomidine, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no or poor activity with bilirubin, dexmedetomidine, diclofenac, levomedetomidine, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
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Substrates: no or poor activity with bilirubin, dexmedetomidine, diclofenac, levomedetomidine, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
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Substrates: no or poor activity with bilirubin, dexmedetomidine, diclofenac, levomedetomidine, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
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Substrates: no or poor activity with bilirubin, dexmedetomidine, diclofenac, levomedetomidine, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
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Substrates: no or poor activity with bilirubin, dexmedetomidine, diclofenac, levomedetomidine, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
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Substrates: no or poor activity with bilirubin, dexmedetomidine, diclofenac, levomedetomidine, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
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Substrates: no or poor activity with bilirubin, dexmedetomidine, diclofenac, levomedetomidine, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
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Substrates: no or poor activity with bilirubin, dexmedetomidine, diclofenac, levomedetomidine, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
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-
Substrates: no or poor activity with bilirubin, dexmedetomidine, diclofenac, levomedetomidine, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, 4-methylumbelliferone, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, 4-methylumbelliferone, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, 4-methylumbelliferone, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, 4-methylumbelliferone, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
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Substrates: no activity with bilirubin, 4-methylumbelliferone, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, 4-methylumbelliferone, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, 4-methylumbelliferone, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, 4-methylumbelliferone, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, 4-methylumbelliferone, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
-
Substrates: no activity with bilirubin, 4-methylumbelliferone, (R)-propranolol, (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
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Substrates: no activity with bilirubin, ethinylestradiol, 17beta- and 17alpha-estradiol, diclofenac, entacapone, 4-methylumbelliferone, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
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additional information
?
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Substrates: no activity with bilirubin, ethinylestradiol, 17beta- and 17alpha-estradiol, diclofenac, entacapone, 4-methylumbelliferone, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, ethinylestradiol, 17beta- and 17alpha-estradiol, diclofenac, entacapone, 4-methylumbelliferone, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, ethinylestradiol, 17beta- and 17alpha-estradiol, diclofenac, entacapone, 4-methylumbelliferone, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, ethinylestradiol, 17beta- and 17alpha-estradiol, diclofenac, entacapone, 4-methylumbelliferone, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, ethinylestradiol, 17beta- and 17alpha-estradiol, diclofenac, entacapone, 4-methylumbelliferone, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, ethinylestradiol, 17beta- and 17alpha-estradiol, diclofenac, entacapone, 4-methylumbelliferone, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, ethinylestradiol, 17beta- and 17alpha-estradiol, diclofenac, entacapone, 4-methylumbelliferone, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, ethinylestradiol, 17beta- and 17alpha-estradiol, diclofenac, entacapone, 4-methylumbelliferone, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
-
Substrates: no activity with bilirubin, ethinylestradiol, 17beta- and 17alpha-estradiol, diclofenac, entacapone, 4-methylumbelliferone, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no or poor activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, levomedetomidine, diclofenac, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no or poor activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, levomedetomidine, diclofenac, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no or poor activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, levomedetomidine, diclofenac, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no or poor activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, levomedetomidine, diclofenac, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no or poor activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, levomedetomidine, diclofenac, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no or poor activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, levomedetomidine, diclofenac, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no or poor activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, levomedetomidine, diclofenac, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no or poor activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, levomedetomidine, diclofenac, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no or poor activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, levomedetomidine, diclofenac, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
-
Substrates: no or poor activity with bilirubin, 17-alpha-estradiol, 17-beta-estradiol, dexmedetomidine, levomedetomidine, diclofenac, indomethacin, (R)-propranolol, and (S)-propranolol, substrate specificities of isozymes, overview
Products: -
?
additional information
?
-
Substrates: no activity with bilirubin, ethinylestradiol, 17-beta-estradiol, dexmedetomidine, and levomedetomidine, substrate specificities of isozymes, overview
Products: -
?
additional information
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Substrates: no activity with bilirubin, ethinylestradiol, 17-beta-estradiol, dexmedetomidine, and levomedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no activity with bilirubin, ethinylestradiol, 17-beta-estradiol, dexmedetomidine, and levomedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no activity with bilirubin, ethinylestradiol, 17-beta-estradiol, dexmedetomidine, and levomedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no activity with bilirubin, ethinylestradiol, 17-beta-estradiol, dexmedetomidine, and levomedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no activity with bilirubin, ethinylestradiol, 17-beta-estradiol, dexmedetomidine, and levomedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no activity with bilirubin, ethinylestradiol, 17-beta-estradiol, dexmedetomidine, and levomedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no activity with bilirubin, ethinylestradiol, 17-beta-estradiol, dexmedetomidine, and levomedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no activity with bilirubin, ethinylestradiol, 17-beta-estradiol, dexmedetomidine, and levomedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no activity with bilirubin, ethinylestradiol, 17-beta-estradiol, dexmedetomidine, and levomedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no or poor activity with bilirubin, levomedetomidine, and dexmedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no or poor activity with bilirubin, levomedetomidine, and dexmedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no or poor activity with bilirubin, levomedetomidine, and dexmedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no or poor activity with bilirubin, levomedetomidine, and dexmedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no or poor activity with bilirubin, levomedetomidine, and dexmedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no or poor activity with bilirubin, levomedetomidine, and dexmedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no or poor activity with bilirubin, levomedetomidine, and dexmedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no or poor activity with bilirubin, levomedetomidine, and dexmedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no or poor activity with bilirubin, levomedetomidine, and dexmedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: no or poor activity with bilirubin, levomedetomidine, and dexmedetomidine, substrate specificities of isozymes, overview
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additional information
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Substrates: activity with all tested bile acids is high with isozyme UGT2A1
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additional information
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Substrates: activity with all tested bile acids is high with isozyme UGT2A1
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additional information
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Q9Y4X1
Substrates: activity with all tested bile acids is high with isozyme UGT2A1
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additional information
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Substrates: activity with all tested bile acids is low with isozyme UGT2A3
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additional information
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Substrates: activity with all tested bile acids is low with isozyme UGT2A3
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additional information
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Q9Y4X1
Substrates: activity with all tested bile acids is low with isozyme UGT2A3
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additional information
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Substrates: UDP-glucuronosyltransferase 2B10 catalyzes N-glucuronidation of amine-containing compounds, substrate specificity overview. Enzyme UGT2B10 preferably conjugates tertiary amines, but not conjugate the tertiary cyclic amine in trifluoperazin, substrate specificity, overview. No activity with desipramine, nortriptyline, carbamazepine, and afloqualone, UGT2B10 does not conjugate the tertiary cyclic amine in trifluoperazine. The affinity and clearance of UGT2B10 for amitriptyline, imipramine, and diphenhydramine are significantly higher than the corresponding values of UGT1A4 and UGT1A3, although the Vmax values of UGT1A4 toward these drugs are considerably higher
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additional information
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Substrates: UDP-glucuronosyltransferase 2B10 catalyzes N-glucuronidation of amine-containing compounds, substrate specificity overview. Enzyme UGT2B10 preferably conjugates tertiary amines, but not conjugate the tertiary cyclic amine in trifluoperazin, substrate specificity, overview. No activity with desipramine, nortriptyline, carbamazepine, and afloqualone, UGT2B10 does not conjugate the tertiary cyclic amine in trifluoperazine. The affinity and clearance of UGT2B10 for amitriptyline, imipramine, and diphenhydramine are significantly higher than the corresponding values of UGT1A4 and UGT1A3, although the Vmax values of UGT1A4 toward these drugs are considerably higher
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additional information
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Substrates: UDP-glucuronosyltransferase 2B10 catalyzes N-glucuronidation of amine-containing compounds, substrate specificity overview. Enzyme UGT2B10 preferably conjugates tertiary amines, but not conjugate the tertiary cyclic amine in trifluoperazin, substrate specificity, overview. No activity with desipramine, nortriptyline, carbamazepine, and afloqualone, UGT2B10 does not conjugate the tertiary cyclic amine in trifluoperazine. The affinity and clearance of UGT2B10 for amitriptyline, imipramine, and diphenhydramine are significantly higher than the corresponding values of UGT1A4 and UGT1A3, although the Vmax values of UGT1A4 toward these drugs are considerably higher
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additional information
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Substrates: UDP-glucuronosyltransferase 2B10 catalyzes N-glucuronidation of amine-containing compounds, substrate specificity overview. Enzyme UGT2B10 preferably conjugates tertiary amines, but not conjugate the tertiary cyclic amine in trifluoperazin, substrate specificity, overview. No activity with desipramine, nortriptyline, carbamazepine, and afloqualone, UGT2B10 does not conjugate the tertiary cyclic amine in trifluoperazine. The affinity and clearance of UGT2B10 for amitriptyline, imipramine, and diphenhydramine are significantly higher than the corresponding values of UGT1A4 and UGT1A3, although the Vmax values of UGT1A4 toward these drugs are considerably higher
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additional information
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Substrates: UDP-glucuronosyltransferase 2B10 catalyzes N-glucuronidation of amine-containing compounds, substrate specificity overview. Enzyme UGT2B10 preferably conjugates tertiary amines, but not conjugate the tertiary cyclic amine in trifluoperazine. The affinity and clearance of UGT2B10 for amitriptyline, imipramine, and diphenhydramine are significantly higher than the corresponding values of UGT1A4 and UGT1A3, although the Vmax values of UGT1A4 toward these drugs are considerably higher
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additional information
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Substrates: UDP-glucuronosyltransferase 2B10 catalyzes N-glucuronidation of amine-containing compounds, substrate specificity overview. Enzyme UGT2B10 preferably conjugates tertiary amines, but not conjugate the tertiary cyclic amine in trifluoperazine. The affinity and clearance of UGT2B10 for amitriptyline, imipramine, and diphenhydramine are significantly higher than the corresponding values of UGT1A4 and UGT1A3, although the Vmax values of UGT1A4 toward these drugs are considerably higher
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additional information
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Substrates: UDP-glucuronosyltransferase 2B10 catalyzes N-glucuronidation of amine-containing compounds, substrate specificity overview. Enzyme UGT2B10 preferably conjugates tertiary amines, but not conjugate the tertiary cyclic amine in trifluoperazine. The affinity and clearance of UGT2B10 for amitriptyline, imipramine, and diphenhydramine are significantly higher than the corresponding values of UGT1A4 and UGT1A3, although the Vmax values of UGT1A4 toward these drugs are considerably higher
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additional information
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Substrates: UDP-glucuronosyltransferase 2B10 catalyzes N-glucuronidation of amine-containing compounds, substrate specificity overview. Enzyme UGT2B10 preferably conjugates tertiary amines, but not conjugate the tertiary cyclic amine in trifluoperazine. The affinity and clearance of UGT2B10 for amitriptyline, imipramine, and diphenhydramine are significantly higher than the corresponding values of UGT1A4 and UGT1A3, although the Vmax values of UGT1A4 toward these drugs are considerably higher
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additional information
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Substrates: UDP-glucuronosyltransferase 2B10 catalyzes N-glucuronidation of amine-containing compounds, substrate specificity overview. Enzyme UGT2B10 preferably conjugates tertiary amines, but not conjugate the tertiary cyclic amine in trifluoperazine. The affinity and clearance of UGT2B10 for amitriptyline, imipramine, and diphenhydramine are significantly higher than the corresponding values of UGT1A4 and UGT1A3, although the Vmax values of UGT1A4 toward these drugs are considerably higher. No activity with diphenhydramine
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additional information
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Substrates: UDP-glucuronosyltransferase 2B10 catalyzes N-glucuronidation of amine-containing compounds, substrate specificity overview. Enzyme UGT2B10 preferably conjugates tertiary amines, but not conjugate the tertiary cyclic amine in trifluoperazine. The affinity and clearance of UGT2B10 for amitriptyline, imipramine, and diphenhydramine are significantly higher than the corresponding values of UGT1A4 and UGT1A3, although the Vmax values of UGT1A4 toward these drugs are considerably higher. No activity with diphenhydramine
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additional information
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Substrates: UDP-glucuronosyltransferase 2B10 catalyzes N-glucuronidation of amine-containing compounds, substrate specificity overview. Enzyme UGT2B10 preferably conjugates tertiary amines, but not conjugate the tertiary cyclic amine in trifluoperazine. The affinity and clearance of UGT2B10 for amitriptyline, imipramine, and diphenhydramine are significantly higher than the corresponding values of UGT1A4 and UGT1A3, although the Vmax values of UGT1A4 toward these drugs are considerably higher. No activity with diphenhydramine
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additional information
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Substrates: UDP-glucuronosyltransferase 2B10 catalyzes N-glucuronidation of amine-containing compounds, substrate specificity overview. Enzyme UGT2B10 preferably conjugates tertiary amines, but not conjugate the tertiary cyclic amine in trifluoperazine. The affinity and clearance of UGT2B10 for amitriptyline, imipramine, and diphenhydramine are significantly higher than the corresponding values of UGT1A4 and UGT1A3, although the Vmax values of UGT1A4 toward these drugs are considerably higher. No activity with diphenhydramine
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additional information
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Substrates: human UGT1A enzymes display unique regioselectivity for the site of glucuronidation and this selectivity is affected strongly by structural differences among the dihydroxychalcones. Several of the UGT1A isoforms show poor reactivity toward the chalcones including UGT1A4, 1A6, and 1A10. UGT1A9 promotes glucuronidation at the 2'-OH-position, and formation of the 2'-O-glucuronide. Several UGT isoforms promote the formation of the 4'-O-glucuronide, particularly UGT1A8, which produces the monoglucuronide in high yield is enhanced for dihydroxychalcones with hydroxy substituents on the A-ring. Although UGT1A8 reacts with 3,2'-dihydroxychalcone and 4,2'-dihydroxychalcone to form 2'-O-glucuronides, the presence of the B-ring hydroxy group at the 4'-position in both cardamonin and 2',4'-dihydroxychalcone renders the OH-2'-position inactive to glucuronidation with the 1A8 isoform. For UGT1A7, hydroxy substituents on the chalcone A-ring enhance the overall yield of glucuronide product and especially promote formation of the corresponding flavanone glucuronide. UGT1A3 strongly promotes glucuronidation at the OH-7 position of the flavanone A-ring in 7-hydroxyflavanone and alpinetin, but leads to much lower glucuronide product yields for flavanones with B-ring hydroxy groups such as 3'-hydroxyflavanone and 4'-hydroxyflavanone. While UGT1A1 catalyzes the formation of glucuronide products in relatively high yields for all of the flavanones studied, in general, glucuronide product formation is less for the flavanones with a B-ring hydroxy group compared to those with an A-ring hydroxy moiety. Isozyme substrate specificity with analysis of multiple product reactions with dihydroxychalcones, product anaysis, detailed overview
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Substrates: no activity with 8-gingerol
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Substrates: no activity with 8-gingerol
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Substrates: no activity with 8-gingerol
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additional information
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Substrates: no activity with 8-gingerol
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additional information
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Substrates: no activity with 8-gingerol
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additional information
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Substrates: no activity with 8-gingerol
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additional information
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Substrates: no activity with 8-gingerol
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Substrates: no activity with 8-gingerol
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additional information
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Substrates: no activity with 8-gingerol
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Substrates: no activity with 8-gingerol
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additional information
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Substrates: no activity with 8-gingerol
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Substrates: no activity with 8-gingerol
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additional information
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Substrates: no activity with 8-gingerol
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additional information
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Substrates: no activity with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity with 8-gingerol and 10-gingerol
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Substrates: no activity by isozyme UGT2B15 with 8-gingerol and 10-gingerol
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Substrates: no activity by isozyme UGT2B15 with 8-gingerol and 10-gingerol
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Substrates: no activity by isozyme UGT2B15 with 8-gingerol and 10-gingerol
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Substrates: no activity by isozyme UGT2B15 with 8-gingerol and 10-gingerol
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Substrates: no activity by isozyme UGT2B15 with 8-gingerol and 10-gingerol
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Substrates: no activity by isozyme UGT2B15 with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity by isozyme UGT2B15 with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity by isozyme UGT2B15 with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity by isozyme UGT2B15 with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity by isozyme UGT2B15 with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity by isozyme UGT2B15 with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity by isozyme UGT2B15 with 8-gingerol and 10-gingerol
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additional information
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Substrates: no activity by isozyme UGT2B15 with 8-gingerol and 10-gingerol
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additional information
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Substrates: isoform UGT2B7 is not capable of converting quercetin
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Substrates: isoform UGT2B7 is not capable of converting quercetin
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Substrates: isoform UGT2B7 is not capable of converting quercetin
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additional information
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Substrates: isoform UGT2B7 is not capable of converting quercetin
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additional information
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Substrates: isoform UGT1A1 does not show activity with zidovudine
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additional information
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Substrates: isoform UGT1A1 does not show activity with zidovudine
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additional information
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Substrates: isoform UGT1A1 does not show activity with zidovudine
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additional information
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Substrates: isoform UGT1A1 does not show activity with zidovudine
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additional information
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Substrates: isoform UGT1A9 does not show activity with zidovudine
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additional information
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Substrates: isoform UGT1A9 does not show activity with zidovudine
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additional information
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Substrates: isoform UGT1A9 does not show activity with zidovudine
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additional information
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Substrates: isoform UGT1A9 does not show activity with zidovudine
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Substrates: isozyme UGT3A1 can also use UDP-N-acetylglucosamine as cosubstrate. UGT3A1-overexpressing microsomes also demonstrates activity against 8-hydroxy-benzo[a]pyrene (8-OH-BaP) and BaP-9,10-diol. Two GlcNAc conjugates are observed for BaP-9,10-diol, likely representing N-acetylglucosaminides at the 9- and 10-diol positions. No detectable glycosylation activity for any other PAH tested is seen with UGT3A1-overexpressing microsomes. No glycosylation is observed for microsomes from the parent HEK293 cell line for 1-OH-pyrene, 8-OH-BaP, or BaP-9,10-diol using UDP-GlcNAc as cosubstrate or when using either UDP-Glc, UDP-Xyl, or UDP-GlcUA as cosubstrate
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Substrates: isozyme UGT3A1 can also use UDP-N-acetylglucosamine as cosubstrate. UGT3A1-overexpressing microsomes also demonstrates activity against 8-hydroxy-benzo[a]pyrene (8-OH-BaP) and BaP-9,10-diol. Two GlcNAc conjugates are observed for BaP-9,10-diol, likely representing N-acetylglucosaminides at the 9- and 10-diol positions. No detectable glycosylation activity for any other PAH tested is seen with UGT3A1-overexpressing microsomes. No glycosylation is observed for microsomes from the parent HEK293 cell line for 1-OH-pyrene, 8-OH-BaP, or BaP-9,10-diol using UDP-GlcNAc as cosubstrate or when using either UDP-Glc, UDP-Xyl, or UDP-GlcUA as cosubstrate
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Substrates: isozyme UGT3A1 can also use UDP-N-acetylglucosamine as cosubstrate. UGT3A1-overexpressing microsomes also demonstrates activity against 8-hydroxy-benzo[a]pyrene (8-OH-BaP) and BaP-9,10-diol. Two GlcNAc conjugates are observed for BaP-9,10-diol, likely representing N-acetylglucosaminides at the 9- and 10-diol positions. No detectable glycosylation activity for any other PAH tested is seen with UGT3A1-overexpressing microsomes. No glycosylation is observed for microsomes from the parent HEK293 cell line for 1-OH-pyrene, 8-OH-BaP, or BaP-9,10-diol using UDP-GlcNAc as cosubstrate or when using either UDP-Glc, UDP-Xyl, or UDP-GlcUA as cosubstrate
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Substrates: UGT3A2 exhibits glycosylation activity against all of the simple and complex polycyclic aromatic hydrocarbons (PAHs)tested. Isozyme UGT3A2 can also use UDP-D-glucose and UDP-D-xylose as cosubstrates. After screening for activity against the PAH substrates, kinetic parameters are determined for UGT3A2 using UDP-Glc or UDPXyl as cosubstrates
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Substrates: UGT3A2 exhibits glycosylation activity against all of the simple and complex polycyclic aromatic hydrocarbons (PAHs)tested. Isozyme UGT3A2 can also use UDP-D-glucose and UDP-D-xylose as cosubstrates. After screening for activity against the PAH substrates, kinetic parameters are determined for UGT3A2 using UDP-Glc or UDPXyl as cosubstrates
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Substrates: UGT3A2 exhibits glycosylation activity against all of the simple and complex polycyclic aromatic hydrocarbons (PAHs)tested. Isozyme UGT3A2 can also use UDP-D-glucose and UDP-D-xylose as cosubstrates. After screening for activity against the PAH substrates, kinetic parameters are determined for UGT3A2 using UDP-Glc or UDPXyl as cosubstrates
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Substrates: chlorophenol mono-glucuronide is detected in the human liver microsomes (HLMs) incubation mixture with cofactor uridine-diphosphate glucuronic acid (UDPGA). HLMs-catalyzed glucuronidation metabolism reaction equations follow Michaelis-Menten or substrate inhibition type. Activity of UGT isozymes, overview
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Substrates: chlorophenol mono-glucuronide is detected in the human liver microsomes (HLMs) incubation mixture with cofactor uridine-diphosphate glucuronic acid (UDPGA). HLMs-catalyzed glucuronidation metabolism reaction equations follow Michaelis-Menten or substrate inhibition type. Activity of UGT isozymes, overview
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additional information
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Substrates: chlorophenol mono-glucuronide is detected in the human liver microsomes (HLMs) incubation mixture with cofactor uridine-diphosphate glucuronic acid (UDPGA). HLMs-catalyzed glucuronidation metabolism reaction equations follow Michaelis-Menten or substrate inhibition type. Activity of UGT isozymes, overview
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additional information
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Substrates: chlorophenol mono-glucuronide is detected in the human liver microsomes (HLMs) incubation mixture with cofactor uridine-diphosphate glucuronic acid (UDPGA). HLMs-catalyzed glucuronidation metabolism reaction equations follow Michaelis-Menten or substrate inhibition type. Activity of UGT isozymes, overview
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additional information
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Substrates: chlorophenol monoglucuronide is detected in the human liver microsomes (HLMs) incubation mixture with cofactor uridine-diphosphate glucuronic acid (UDPGA). HLMs-catalyzed glucuronidation metabolism reaction equations follow Michaelis-Menten or substrate inhibition type. Activity of UGT isozymes, overview
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additional information
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Substrates: chlorophenol monoglucuronide is detected in the human liver microsomes (HLMs) incubation mixture with cofactor uridine-diphosphate glucuronic acid (UDPGA). HLMs-catalyzed glucuronidation metabolism reaction equations follow Michaelis-Menten or substrate inhibition type. Activity of UGT isozymes, overview
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additional information
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Substrates: chlorophenol monoglucuronide is detected in the human liver microsomes (HLMs) incubation mixture with cofactor uridine-diphosphate glucuronic acid (UDPGA). HLMs-catalyzed glucuronidation metabolism reaction equations follow Michaelis-Menten or substrate inhibition type. Activity of UGT isozymes, overview
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additional information
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Substrates: chlorophenol monoglucuronide is detected in the human liver microsomes (HLMs) incubation mixture with cofactor uridine-diphosphate glucuronic acid (UDPGA). HLMs-catalyzed glucuronidation metabolism reaction equations follow Michaelis-Menten or substrate inhibition type. Activity of UGT isozymes, overview
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additional information
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Substrates: analysis of plasma concentration-time profiles of the 7 substrate drugs and their glucuronide metabolites in severe combined immunodeficiency mice transplanted with human-derived hepatocytes
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11alpha-hydroxyprogesterone + UDP-glucuronate
UDP + 11alpha-hydroxyprogesterone-11-O-D-glucuronate
Substrates: -
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16alpha-hydroxyprogesterone + UDP-glucuronate
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Substrates: UGT2B15 and UGT2B17 are the major enzyme forms involved in the high-affinity component of 16alpha-hydroxyprogesterone glucuronidation
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16alpha-hydroxyprogesterone + UDP-glucuronate
UDP + 16alpha-hydroxyprgesterone-16-O-D-glucuronate
2 UDP-D-glucuronate + 2 dexmedetomidine
2 UDP + dexmedetomidine N1-beta-D-glucuronoside + dexmedetomidine N3-beta-D-glucuronoside
Substrates: the major metabolic pathway of dexmedetomidine, i.e. (4S)-[1-(2,3-dimethylphenyl)ethyl]-1H-imidazole, in humans is N-glucuronidation at the imidazolate nitrogens to N3- and N1-glucuronides
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2 UDP-D-glucuronate + 2 levomedetomidine
2 UDP + levomedetomidine N1-beta-D-glucuronoside + dexmedetomidine N3-beta-D-glucuronoside
Substrates: the major metabolic pathway of levomedetomidine, i.e. (4R)-[1-(2,3-dimethylphenyl)ethyl]-1H-imidazole, in humans is N-glucuronidation at the imidazolate nitrogens to N3-glucuronide
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2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid + UDP-glucuronate
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2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid + UDPglucuronate
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Substrates: glucuronidation of 2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid is mainly catalyzed by UGT1A1, UGT1A9, and UGT2B7 in the liver, and by UGT1A1, UGT1A3, and UGT2B7 in the intestine in humans
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21-hydroxyprogesterone + UDP-glucuronate
UDP + 21-hydroxyprogesterone-21-O-D-glucuronate
Substrates: -
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6alpha-hydroxyprogesterone + UDP-glucuronate
UDP + 6alpha-hydroxyprogesteron-6-O-alpha-D-glucuronate
Substrates: -
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bilirubin + UDPglucuronate
UDP + bilirubin O-glucuronide
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Substrates: -
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estrogen + UDP-glucuronate
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Substrates: UDP-glucuronosyltransferase 1A10 has been identified as the major isoform involved in the biotransformation of a wide range of phenolic substrates, including native estrogens and their oxidized metabolites
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etoposide + UDP-glucuronate
UDP + etoposide glucuronide
Substrates: UGT1A1 is principally responsible for the formation of etoposide glucuronides, mainly in the form of phenolic glucuronide
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testosterone + UDP-glucuronate
UDP + testosterone beta-D-glucuronoside
Substrates: UGT2B15 and UGT2B17 are the major enzyme forms involved in human liver microsomal testosterone 17beta-glucuronidation
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UDP-alpha-D-glucuronate + (S)-naproxen
UDP + beta-D-glucuronosyl (S)-naproxen
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Substrates: -
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UDP-alpha-D-glucuronate + 3-hydroxyflavone
UDP + 3-[(beta-D-glucopyranurnosyl)oxy]-flavone
Substrates: isozyme UGT1A1
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UDP-D-glucuronate + 17beta-estradiol
UDP + 17beta-estradiol 3-O-beta-D-glucuronoside
Substrates: -
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UDP-D-glucuronate + 3-hydroxydesloratadine
UDP + 3-hydroxydesloratadine beta-O-D-glucuronoside
Substrates: specific substrate of isozyme UGT1A8
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UDP-D-glucuronate + 4'-hydroxy-warfarin
UDP + 4'-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A10
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UDP-D-glucuronate + 4-hydroxy-N-desmethyl-tamoxifen
UDP + 4-hydroxy-N-desmethyl-tamoxifen beta-D-glucuronoside
Substrates: the enzyme is involved in metabolism and elimination of tamoxifen, TAM, and its major active metabolites 4-hydroxytamoxifen and 4-hydroxy-N-desmethyl-tamoxifen, i.e. endoxifen, by glucuronidation, overview
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UDP-D-glucuronate + 6-hydroxy-warfarin
UDP + 6-hydroxy-warfarin beta-D-glucuronoside
UDP-D-glucuronate + 7-hydroxy-warfarin
UDP + 7-hydroxy-warfarin beta-D-glucuronoside
UDP-D-glucuronate + 8-hydroxy-warfarin
UDP + 8-hydroxy-warfarin beta-D-glucuronoside
UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
UDP-D-glucuronate + androstane-3alpha,17beta-diol
UDP + ?
UDP-D-glucuronate + androsterone
UDP + androsterone 3-O-beta-D-glucuronoside
UDP-D-glucuronate + bilirubin
UDP + bilirubin beta-D-glucuronoside
Substrates: isozyme UGT1A1
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UDP-D-glucuronate + bisdemethoxy-curcumin
UDP + bisdemethoxy-curcumin phenolic beta-D-monoglucuronide
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Substrates: -
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UDP-D-glucuronate + chenodeoxycholic acid
UDP + hyodeoxycholic acid 6-O-glucuronoside
Substrates: isozyme UGT2A3
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UDP-D-glucuronate + cis-4-hydroxytamoxifen
UDP + 4-hydroxytamoxifen beta-D-glucuronoside
Substrates: the enzyme is involved in metabolism and elimination of tamoxifen, TAM, and its major active metabolites 4-hydroxytamoxifen and 4-hydroxy-N-desmethyl-tamoxifen, i.e. endoxifen, by glucuronidation, overview
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UDP-D-glucuronate + cotinine
UDP + ?
Substrates: isozyme UGT2B10, cotinine is exclusively glucuronized in liver, no activity in intestinal microsomes
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UDP-D-glucuronate + curcumin
UDP + curcumin phenolic beta-D-monoglucuronide
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Substrates: glucuronidation is an important pathway in the metabolism of curcumin
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UDP-D-glucuronate + dehydrotestosterone
UDP + dehydrotestosterone 17-O-beta-D-glucuronoside
UDP-D-glucuronate + demethoxy-curcumin
UDP + demethoxy-curcumin phenolic beta-D-monoglucuronide
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Substrates: -
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UDP-D-glucuronate + deoxycholic acid
UDP + hyodeoxycholic acid 6-O-glucuronoside
Substrates: isozyme UGT2A3
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UDP-D-glucuronate + dihydrotestosterone
UDP + dihydrotestosterone 17-O-beta-D-glucuronoside
Substrates: in epithelial cells of the human prostate
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UDP-D-glucuronate + estradiol
UDP + estradiol 3-O-beta-D-glucuronoside
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Substrates: isozymes UGT1A1 and UGT1A9
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UDP-D-glucuronate + estradiol
UDP + estradiol-3-beta-D-glucuronoside
Substrates: liver microsomes
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UDP-D-glucuronate + flurbiprofen
UDP + flurbiprofen beta-D-glucuronoside
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Substrates: isozyme UGT2B7
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UDP-D-glucuronate + frusemide
UDP + frusemide beta-D-glucuronoside
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Substrates: -
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UDP-D-glucuronate + gemfibrozil
UDP + gemfibrozil beta-D-glucuronoside
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Substrates: gemfibrozil is a fibrate hypolipidemic agent, isozyme UGT2B7 in the liver
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UDP-D-glucuronate + hyodeoxycholic acid
UDP + hyodeoxycholic acid 6-O-glucuronoside
Substrates: isozyme UGT2A3
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UDP-D-glucuronate + labetalol
UDP + ?
UDP-D-glucuronate + morphine
UDP + morphine 3-O-beta-D-glucuronoside
UDP-D-glucuronate + morphine
UDP + morphine 6-beta-D-glucuronoside
Substrates: the metabolic conversion of morphine to morphine-6-glucuronide plays a significant role in mediation of the clinical effect of morphine because of the superior analgesic effect of morphine-6-glucuronide
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UDP-D-glucuronate + nicotine
UDP + ?
Substrates: isozyme UGT2B10, nicotine is mainly glucuronized in liver, very low activity in intestinal microsomes
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UDP-D-glucuronate + propofol
UDP + propofol beta-D-glucuronoside
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Substrates: isozymes UGT1A1 and UGT1A9
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UDP-D-glucuronate + protocatechuic aldehyde
UDP + ?
Substrates: -
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UDP-D-glucuronate + serotonin
UDP + serotonin beta-D-glucuronoside
Substrates: isozyme UGT1A6
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UDP-D-glucuronate + tamoxifen + H+
UDP + tamoxifen beta-D-glucuronoside
Substrates: the enzyme is involved in metabolism and elimination of tamoxifen, TAM, and its major active metabolites 4-hydroxytamoxifen and 4-hydroxy-N-desmethyl-tamoxifen, i.e. endoxifen, by glucuronidation, overview
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UDP-D-glucuronate + thyroxine
UDP + thyroxine beta-D-glucuronoside
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Substrates: glucuronidation of the thyroid hormone thyroxine, T4, in the human liver, the T4 glucuronidation activities of recombinant human UGT isoforms and microsomes
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UDP-D-glucuronate + trans-4-hydroxytamoxifen
UDP + 4-hydroxytamoxifen beta-D-glucuronoside
Substrates: the enzyme is involved in metabolism and elimination of tamoxifen, TAM, and its major active metabolites 4-hydroxytamoxifen and 4-hydroxy-N-desmethyl-tamoxifen, i.e. endoxifen, by glucuronidation, overview
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UDP-D-glucuronate + ursodeoxycholic acid
UDP + hyodeoxycholic acid 6-O-glucuronoside
Substrates: isozyme UGT2A3
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UDP-glucuronate + (E)-2,4-dimethoxy-6-(4-methoxystyryl)benzaldehyde oxime
UDP + 1-O-[(E)-2,4-dimethoxy-6-(4-methoxystyryl)benzaldehyde oxime]-beta-D-glucuronate
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Substrates: i.e. NI-ST-05, low activity, NI-ST-05 forms a distinct N-O-glucuronide. NI-ST-05 is primarily metabolized by an extrahepatic enzyme, UGT1A10
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UDP-glucuronate + (E)-3-(3-hydroxy-4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)acrylic acid
UDP + ?
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Substrates: i.e. NI-12a, low activity, NI-12a is glucuronidated at both the -COOH and -OH functions. NI-12a is primarily metabolized by the hepatic and renal enzyme UGT1A9
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UDP-glucuronate + 10-gingerol
UDP + 10-gingerol 4'-O-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
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UDP-glucuronate + 10-gingerol
UDP + 10-gingerol 5-O-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
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UDP-glucuronate + 3-epideacetycinobufagin
UDP + 3-epideacetycinobufagin 3-beta-D-glucuronoside
Substrates: 3-epideacetycinobufagin is a highly isoform-specific probe substrate for 3-glucuronidation mediated by UDP-glucuronosyltransferase 2B7 determined in recombinant UGT supersomes, overview
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UDP-glucuronate + 4-hydroxy-estrone
UDP + ?
Substrates: glucuronidation of 4-hydroxylated estrone is significantly reduced in breast carcinomas compared to healthy
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UDP-glucuronate + 6-gingerol
UDP + 6-gingerol 4'-O-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
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UDP-glucuronate + 6-gingerol
UDP + 6-gingerol 5-O-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
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UDP-glucuronate + 7-ethyl-10-hydroxycamptothecin
UDP + 7-ethyl-10-hydroxycamptothecin 10-O-beta-D-glucuronoside
Substrates: i.e. SN-38, an active metabolite of irinotecan
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UDP-glucuronate + 8-gingerol
UDP + 8-gingerol 4'-O-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
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UDP-glucuronate + 8-gingerol
UDP + 8-gingerol 5-O-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
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UDP-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
UDP-glucuronate + acceptor
UDP + acceptor beta-glucuronoside
UDP-glucuronate + estriol
UDP + estriol beta-D-glucuronoside
Substrates: -
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UDP-glucuronate + ethanol
UDP + ethyl beta-D-glucuronoside
Substrates: -
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UDP-glucuronate + genistein
UDP + genistein beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + gingerol
UDP + gingerol 4'-O-beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
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UDP-glucuronate + morphine
UDP + morphine-3-beta-D-glucuronide
UDP-glucuronate + morphine
UDP + morphine-6-beta-D-glucuronide
Substrates: -
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UDP-glucuronate + mycophenolic acid
UDP + mycophenolic acid-acyl-glucuronide
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Substrates: mycophenolic acid is the active metabolite of immunosuppressant mycophenolate mofetil
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UDP-glucuronate + mycophenolic acid
UDP + mycophenolic acid-phenyl-glucuronide
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Substrates: mycophenolic acid is the active metabolite of immunosuppressant mycophenolate mofetil
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UDP-glucuronate + propofol
UDP + propofol beta-D-glucuronoside
UDP-glucuronate + serotonin
UDP + serotonin beta-glucuronoside
Substrates: isozyme UGT2B7
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UDP-glucuronate + tamoxifen
UDP + tamoxifen N-beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + trans-resveratrol
UDP + trans-resveratrol beta-D-glucuronoside
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Substrates: -
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UDP-glucuronate + zidovudine
UDP + zidovudine beta-D-glucuronoside
UDP-glucuronic acid + bilirubin
UDP + bilirubin-glucuronoside
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Substrates: UGT1A1
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UDP-glucuronose + chlorophenol
UDP + chlorophenyl beta-D-glucuronide
Substrates: -
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UDP-glucuronose + chlorophenol
UDP + chlorophenyl beta-D-glucuronoide
Substrates: -
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UDPglucuronate + naproxen
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Substrates: UGT2B7 is responsible for human hepatic naproxen acyl glucuronidation, which is the primary elimination pathway for this drug
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additional information
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16alpha-hydroxyprogesterone + UDP-glucuronate

UDP + 16alpha-hydroxyprgesterone-16-O-D-glucuronate
Substrates: UGT2B15 and UGT2B17 are the major enzyme forms involved in the high-affinity component of 16alpha-hydroxyprogesterone glucuronidation
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16alpha-hydroxyprogesterone + UDP-glucuronate
UDP + 16alpha-hydroxyprgesterone-16-O-D-glucuronate
Substrates: -
Products: -
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2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid + UDP-glucuronate

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Substrates: glucuronidation of 2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid is mainly catalyzed by UGT1A1, UGT1A9, and UGT2B7 in the liver, and by UGT1A1, UGT1A3, and UGT2B7 in the intestine i humans
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2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid + UDP-glucuronate
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Substrates: glucuronidation of 2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid is mainly catalyzed by UGT1A1, UGT1A9, and UGT2B7 in the liver, and by UGT1A1, UGT1A3, and UGT2B7 in the intestine
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UDP-D-glucuronate + 6-hydroxy-warfarin

UDP + 6-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A1
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UDP-D-glucuronate + 6-hydroxy-warfarin
UDP + 6-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A10
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UDP-D-glucuronate + 7-hydroxy-warfarin

UDP + 7-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A1
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UDP-D-glucuronate + 7-hydroxy-warfarin
UDP + 7-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A10
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UDP-D-glucuronate + 8-hydroxy-warfarin

UDP + 8-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A9
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UDP-D-glucuronate + 8-hydroxy-warfarin
UDP + 8-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A1
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UDP-D-glucuronate + 8-hydroxy-warfarin
UDP + 8-hydroxy-warfarin beta-D-glucuronoside
Substrates: substrate of isozyme UGT1A10
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UDP-D-glucuronate + acceptor

UDP + acceptor beta-D-glucuronoside
Substrates: the enzyme plays a key role in the metabolism of endogenous and exogenous compounds
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
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Substrates: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
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Substrates: glucuronidation is a major phase II conjugation reaction of numerous xenobiotic as well as endobiotic compounds
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
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Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
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Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
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Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
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Substrates: protein kinases are involved in UGT regulation, UGTs inactivate aromatic-like metabolites and a vast number of dietary and environmental chemicals, which reduces the risk of toxicities, mutagenesis, and carcinogenesis, primarily in liver, kidney, and gastrointestinal tract, overview
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
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Substrates: potential role of UGTs in regulating aldosterone
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: conjugation by UDP-glucuronosyltransferase is the major pathway of androgen metabolism and elimination in the human
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
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Substrates: UDP-glucuronosyltransferases play important roles in the metabolism, detoxification,and clearance of many different xenobiotics, including drugs and endogenous compounds
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
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Substrates: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: UGT isozyme substrate specificity, overview
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: UDP-glucuronosyltransferases are membrane-bound proteins localized to the endoplasmic reticulum and catalyze the formation of beta-D-glucopyranosiduronic acids using UDP-D-glucuronic acid and acceptor substrates such as drugs, steroids, bile acids, xenobiotics, and dietary nutrients
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: the enzyme is involved in detoxification reactions
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
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UDP-D-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
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Substrates: -
Products: -
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UDP-D-glucuronate + androstane-3alpha,17beta-diol

UDP + ?
Substrates: in epithelial cells of the human prostate
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UDP-D-glucuronate + androstane-3alpha,17beta-diol
UDP + ?
Substrates: isozyme UGT2B7in the liver
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UDP-D-glucuronate + androstane-3alpha,17beta-diol
UDP + ?
Substrates: isozyme UGT2B15 in the liver
Products: -
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UDP-D-glucuronate + androstane-3alpha,17beta-diol
UDP + ?
Substrates: isozyme UGT2B17 in the liver
Products: -
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UDP-D-glucuronate + androsterone

UDP + androsterone 3-O-beta-D-glucuronoside
Substrates: in epithelial cells of the human prostate
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UDP-D-glucuronate + androsterone
UDP + androsterone 3-O-beta-D-glucuronoside
Substrates: isozyme UGT2B7in the liver
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UDP-D-glucuronate + androsterone
UDP + androsterone 3-O-beta-D-glucuronoside
Substrates: isozyme UGT2B15 in the liver
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UDP-D-glucuronate + androsterone
UDP + androsterone 3-O-beta-D-glucuronoside
Substrates: isozyme UGT2B17 in the liver
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UDP-D-glucuronate + dehydrotestosterone

UDP + dehydrotestosterone 17-O-beta-D-glucuronoside
Substrates: isozyme UGT2B7in the liver
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UDP-D-glucuronate + dehydrotestosterone
UDP + dehydrotestosterone 17-O-beta-D-glucuronoside
Substrates: isozyme UGT2B15in the liver
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UDP-D-glucuronate + dehydrotestosterone
UDP + dehydrotestosterone 17-O-beta-D-glucuronoside
Substrates: isozyme UGT2B17in the liver
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UDP-D-glucuronate + labetalol

UDP + ?
Substrates: the reaction is catalyzed mainly by isozymes UGT1A1 and UGT2B7, potential role for progesterone in regulating labetalol elimination by modulating the expression of UGT1A1, leading to enhanced drug metabolism during pregnancy, overview
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UDP-D-glucuronate + labetalol
UDP + ?
Substrates: -
Products: -
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UDP-D-glucuronate + labetalol
UDP + ?
Substrates: the reaction is catalyzed mainly by isozymes UGT1A1 and UGT2B7, overview
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UDP-D-glucuronate + morphine

UDP + morphine 3-O-beta-D-glucuronoside
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Substrates: isozyme UGT2B7
Products: -
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UDP-D-glucuronate + morphine
UDP + morphine 3-O-beta-D-glucuronoside
Substrates: isozyme UGT1A1
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UDP-glucuronate + acceptor

UDP + acceptor beta-D-glucuronoside
Substrates: UGT1A10 is an important detoxifier of polycyclic aromatic hydrocarbons
Products: -
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UDP-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + acceptor
UDP + acceptor beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + acceptor

UDP + acceptor beta-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + acceptor
UDP + acceptor beta-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + morphine

UDP + morphine-3-beta-D-glucuronide
Substrates: regioselectivity of activity is altered by cytochrome P450 enzyme CYP3A4 so that the ratio of morphine activation/detoxification is increased
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UDP-glucuronate + morphine
UDP + morphine-3-beta-D-glucuronide
Substrates: -
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UDP-glucuronate + propofol

UDP + propofol beta-D-glucuronoside
Substrates: -
Products: -
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UDP-glucuronate + propofol
UDP + propofol beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
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UDP-glucuronate + zidovudine

UDP + zidovudine beta-D-glucuronoside
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UDP-glucuronate + zidovudine
UDP + zidovudine beta-D-glucuronoside
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 Substrates: -
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Substrates: wide variety of endogenous steroidal hormones, bile acids, retinoids and tyroid hormones glucuronidated by isozymes of UGT1A family
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Substrates: elimination of lipid-soluble endogenous compounds and xenobiotics
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Substrates: elimination of lipid-soluble endogenous compounds and xenobiotics
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Substrates: elimination of lipid-soluble endogenous compounds and xenobiotics
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Substrates: steroid hormones, bile acids, all trans retinoic acids and fatty acids glucuronidated by isozymes of UGTB2 family
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Substrates: certain endogenous estrogens glucuronidated by UGT1.1 at 3-hydroxyl group of the A ring of steroids
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Substrates: isozyme UGT2B7 is involved in metabolism of mineralocorticoid and glucocorticoid hormones, two-cell mechanism of aldosterone action and metabolism in the kidney
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Substrates: isozyme UGT2B7 is involved in metabolism of mineralocorticoid and glucocorticoid hormones, two-cell mechanism of aldosterone action and metabolism in the kidney
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Substrates: isozymes are involved in detoxification of metabolites, drugs, toxins, and environmental chemicals via conjugation to glucuronic acid, physiological roles and overlapping activities
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Substrates: isozymes are involved in detoxification of metabolites, drugs, toxins, and environmental chemicals via conjugation to glucuronic acid, physiological roles and overlapping activities
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Substrates: isozymes are involved in detoxification of metabolites, drugs, toxins, and environmental chemicals via conjugation to glucuronic acid, physiological roles and overlapping activities
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Substrates: isozymes are involved in detoxification of metabolites, drugs, toxins, and environmental chemicals via conjugation to glucuronic acid, physiological roles and overlapping activities
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Substrates: isozymes are involved in detoxification of metabolites, drugs, toxins, and environmental chemicals via conjugation to glucuronic acid, physiological roles and overlapping activities
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Substrates: enzyme are involved in biosynthesis of HNK-1 carbohydrate
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Substrates: isozymes facilitate the excretion of estrogens to glucuronides, the most abundant estrogen conjugates
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Substrates: the enzyme is involved acyl glucuronidation, an important metabolic pathway for fluoroquinolone antobiotics
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Substrates: the enzyme is involved acyl glucuronidation, an important metabolic pathway for fluoroquinolone antobiotics
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Substrates: the enzyme is involved acyl glucuronidation, an important metabolic pathway for fluoroquinolone antobiotics
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Substrates: the enzyme is involved acyl glucuronidation, an important metabolic pathway for fluoroquinolone antobiotics
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Substrates: the enzyme is involved acyl glucuronidation, an important metabolic pathway for fluoroquinolone antobiotics
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Substrates: enzyme UGT2B7 plays a crucial role in drug detoxificiation
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Substrates: isozyme UGT2B7 is the major isozyme involved in metabolization of morphine in the liver
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Substrates: isozyme UGT2B7 is involved in glucuronidation of a wide array of clinically important drugs and endogenous compounds in humans
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Substrates: glucuronidation by the UDP glucuronosyltransferase 1A enzymes is a major pathway for elimination of drugs and endogenous substances, such as bilirubin
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Substrates: direct inhibition of UGT1A1-mediated bilirubin glucuronidation may provide a mechanism for the reversible hyperbilirubinemia associated with administration of atazanavir as well as indinavir
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Substrates: isozyme UGT2B15 is a critical enzyme for the local inactivation of androgens and major determinants of the androgen response in prostate cancer LNCaP cells, overview
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Substrates: isozyme UGT2B15 is a critical enzyme for the local inactivation of androgens and major determinants of the androgen response in prostate cancer LNCaP cells, overview
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Substrates: isozyme UGT2B15 is a critical enzyme for the local inactivation of androgens and major determinants of the androgen response in prostate cancer LNCaP cells, overview
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Substrates: The phenolic glucuronidation of the curcuminoids is predominantly catalyzed by hepatic isozyme UGT1A1 and intestinal isozymes UGT1A8 and UGT1A10, whereas isozymes UGT1A9, UGT2B7, and UGT1A8 exhibit high activities for hexahydro-curcuminoids, substrate specificities of recombinant isozymes in insect cell microsomes, overview
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Substrates: UGTs play an important role in the defense against potentially hazardous xenobiotics, and they participate in the metabolism and homeostasis of many endogenous compounds, including bilirubin and steroid hormones, overview
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Substrates: UGTs play an important role in the defense against potentially hazardous xenobiotics, and they participate in the metabolism and homeostasis of many endogenous compounds, including bilirubin and steroid hormones, overview
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Substrates: UGTs play an important role in the defense against potentially hazardous xenobiotics, and they participate in the metabolism and homeostasis of many endogenous compounds, including bilirubin and steroid hormones, overview
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Substrates: UGTs play an important role in the defense against potentially hazardous xenobiotics, and they participate in the metabolism and homeostasis of many endogenous compounds, including bilirubin and steroid hormones, overview
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Substrates: the role of UGT enzymes in the liver is recognized as a highly efficient and constitutive mechanism of detoxification of endogenous and exogenous compounds, particularly for steroid hormones, metabolism of adrenal and testicular steroid hormones, overview
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Substrates: the role of UGT enzymes in the liver is recognized as a highly efficient and constitutive mechanism of detoxification of endogenous and exogenous compounds, particularly for steroid hormones, metabolism of adrenal and testicular steroid hormones, overview
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Substrates: the role of UGT enzymes in the liver is recognized as a highly efficient and constitutive mechanism of detoxification of endogenous and exogenous compounds, particularly for steroid hormones, metabolism of adrenal and testicular steroid hormones, overview
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Substrates: regulation of isozyme UGT1A1 by progesterone and its impact on labetalol elimination, overview
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Substrates: regulation of isozyme UGT1A1 by progesterone and its impact on labetalol elimination, overview
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Substrates: regulation of isozyme UGT1A1 by progesterone and its impact on labetalol elimination, overview
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Substrates: regulation of isozyme UGT1A1 by progesterone and its impact on labetalol elimination, overview
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Substrates: regulation of isozyme UGT1A1 by progesterone and its impact on labetalol elimination, overview
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Substrates: regulation of isozyme UGT1A1 by progesterone and its impact on labetalol elimination, overview
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Substrates: regulation of isozyme UGT1A1 by progesterone and its impact on labetalol elimination, overview
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the UGT1A family of proteins forms oligomerized complexes in the membrane, a property that may influence function and substrate selectivity
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Substrates: the enzyme is involved in clearance and detoxification of many chemical compounds, overview
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Substrates: isozyme UGT2B17 is a critical enzyme for the local inactivation of androgens and major determinants of the androgen response in prostate cancer LNCaP cells, overview
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Substrates: isozyme UGT2B17 is a critical enzyme for the local inactivation of androgens and major determinants of the androgen response in prostate cancer LNCaP cells, overview
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Substrates: isozyme UGT2B17 is a critical enzyme for the local inactivation of androgens and major determinants of the androgen response in prostate cancer LNCaP cells, overview
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Substrates: no activity with (E)-4-(3,5-dimethoxystyryl)-2,6-dinitrophenol, i.e. DNR-1, glucuronide formation is verified by beta-glucuronidase hydrolysis and LC-MS/MS analysis
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Substrates: trans-Resveratrol has powerful antioxidant, anti-inflammatory, anticarcinogenic, and antiaging properties, but its use as a therapeutic agent is limited by its rapid metabolism into its conjugated forms by UDP-glucuronosyltransferases. The limited bioavailability of tRes can be improved by modifying its structure to create analogues which can be glucuronidated at a lower rate than tRes itself. Three synthetic stilbenoids ((E)-3-(3-hydroxy-4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)acrylic acid, (E)-2,4-dimethoxy-6-(4-methoxystyryl)benzaldehyde oxime, and (E)-4-(3,5-dimethoxystyryl)-2,6-dinitrophenol) are designed based on the structure of tRes and synthesized. UDP-glucuronosyltransferases recognize and glucuronidate trans-resveratrol at each of the 3 hydroxyl groups attached to its aromatic rings
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Substrates: the human UGTs of subfamily 2A, UGT2A1, 2A2, and 2A3, show bile acid-conjugating activity
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Substrates: the human UGTs of subfamily 2A, UGT2A1, 2A2, and 2A3, show bile acid-conjugating activity
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Q9Y4X1
Substrates: the human UGTs of subfamily 2A, UGT2A1, 2A2, and 2A3, show bile acid-conjugating activity
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. Formation of 5-O-glucuronide is mainly catalysed by UGT1A9
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B7 is the only isozyme that generates glucuronides at both 4'-OH and 5-OH sites, although a strong position preference is observed with 4'-OH of over 80.2%
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
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Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A1 generates glucuronides at 4'-OH sites
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Substrates: no activity with gingerols by enzyme UGT1A3
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Substrates: no activity with gingerols by enzyme UGT1A3
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Substrates: no activity with gingerols by enzyme UGT1A3
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Substrates: no activity with gingerols by enzyme UGT1A3
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Substrates: no activity with gingerols by enzyme UGT1A3
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Substrates: no activity with gingerols by enzyme UGT1A3
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Substrates: no activity with gingerols by enzyme UGT1A3
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Substrates: no activity with gingerols by enzyme UGT1A3
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Substrates: no activity with gingerols by enzyme UGT1A3
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Substrates: no activity with gingerols by enzyme UGT1A3
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Substrates: no activity with gingerols by enzyme UGT1A3
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Substrates: no activity with gingerols by enzyme UGT1A3
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Substrates: no activity with gingerols by enzyme UGT1A3
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Substrates: no activity with gingerols by enzyme UGT1A4
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Substrates: no activity with gingerols by enzyme UGT1A4
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Substrates: no activity with gingerols by enzyme UGT1A4
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Substrates: no activity with gingerols by enzyme UGT1A4
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Substrates: no activity with gingerols by enzyme UGT1A4
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Substrates: no activity with gingerols by enzyme UGT1A4
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Substrates: no activity with gingerols by enzyme UGT1A4
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Substrates: no activity with gingerols by enzyme UGT1A4
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Substrates: no activity with gingerols by enzyme UGT1A4
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Substrates: no activity with gingerols by enzyme UGT1A4
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Substrates: no activity with gingerols by enzyme UGT1A4
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Substrates: no activity with gingerols by enzyme UGT1A4
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Substrates: no activity with gingerols by enzyme UGT1A4
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Substrates: no activity with gingerols by enzyme UGT1A6
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Substrates: no activity with gingerols by enzyme UGT1A6
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Substrates: no activity with gingerols by enzyme UGT1A6
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Substrates: no activity with gingerols by enzyme UGT1A6
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Substrates: no activity with gingerols by enzyme UGT1A6
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Substrates: no activity with gingerols by enzyme UGT1A6
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Substrates: no activity with gingerols by enzyme UGT1A6
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Substrates: no activity with gingerols by enzyme UGT1A6
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Substrates: no activity with gingerols by enzyme UGT1A6
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Substrates: no activity with gingerols by enzyme UGT1A6
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Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
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additional information
?
-
Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
?
additional information
?
-
-
Substrates: no activity with gingerols by enzyme UGT1A6
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A7 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A8 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT1A10 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
-
Substrates: no activity with gingerols by enzyme UGT2B4
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B15 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
?
additional information
?
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-
Substrates: main UGT enzymes involved in regioselective glucuronidation of gingerols are isozymes UGT1A9 and UGT2B7. UGT2B17 generates glucuronides at 4'-OH sites
Products: -
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additional information
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Substrates: morphine glucuronidation and glucosidation represent complementary metabolic pathways that are both catalyzed by UDP-glucuronosyltransferase 2B7. Glucuronidation is the dominant metabolic pathway because the binding affinity of UDP-glucuronic acid to UGT2B7 is higher than that of UDPglucose
Products: -
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additional information
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Substrates: morphine glucuronidation and glucosidation represent complementary metabolic pathways that are both catalyzed by UDP-glucuronosyltransferase 2B7. Glucuronidation is the dominant metabolic pathway because the binding affinity of UDP-glucuronic acid to UGT2B7 is higher than that of UDPglucose
Products: -
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((2R)-2-hydroxy-2-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]ethyl)phosphonic acid
-
-
((2S)-2-hydroxy-2-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]ethyl)phosphonic acid
-
-
((3R)-3-hydroxy-3-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propyl)phosphonic acid
-
-
((3S)-3-hydroxy-3-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propyl)phosphonic acid
-
-
(+)-longifolol
a tricyclic sesquiterpenol
(1R)-1-cyclopropyl-2-methylpropan-1-ol
IC50: 0.0004 mM
(1R)-1-cyclopropylbut-3-en-1-ol
IC50: 0.0004 mM; IC50: 0.0009 mM
(1R)-1-cyclopropylbut-3-ene-1,3-diol
IC50: 0.0004 mM
(1R)-1-cyclopropylethanol
IC50: 0.0005 mM
(1R)-1-cyclopropylprop-2-en-1-ol
IC50: 0.0003 mM
(1R)-1-cyclopropylpropan-1-ol
IC50: 0.0002 mM
(1R)-1-cyclopropylpropane-1,3-diol
IC50: 0.0002 mM
(1R)-1-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]but-3-en-1-ol
-
-
(1R)-1-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]ethanol
-
-
(1R)-1-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]prop-2-en-1-ol
-
-
(1R)-1-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propan-1-ol
-
-
(1R)-1-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propane-1,3-diol
-
-
(1R)-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]but-3-en-1-ol
-
-
(1R)-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]ethan
-
-
(1R)-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]prop-2-en-1-ol
-
-
(1R)-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propan-1-ol
-
-
(1R)-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propane-1,3-diol
-
-
(1R)-2,2-dimethyl-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propan-1-ol
-
-
(1R)-2-chloro-1-cyclopropylethanol
IC50: 0.0002 mM
(1R)-2-chloro-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]ethanol
-
-
(1R)-2-methyl-1-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propan-1-ol
-
-
(1R)-2-methyl-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propan-1-ol
-
-
(1S)-1-cyclopropyl-2,2-dimethylpropan-1-ol
IC50: 0.0002 mM
(1S)-1-cyclopropyl-2-methylpropan-1-ol
IC50: 0.0004 mM
(1S)-1-cyclopropylbut-3-en-1-ol
IC50: 0.0002 mM
(1S)-1-cyclopropylethanol
IC50: 0.0007 mM
(1S)-1-cyclopropylprop-2-en-1-ol
IC50: 0.0006 mM
(1S)-1-cyclopropylpropan-1-ol
IC50: 0.0005 mM
(1S)-1-cyclopropylpropane-1,3-diol
IC50: 0.0003 mM
(1S)-1-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propane-1,3-diol
-
-
(1S)-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]but-3-en-1-ol
-
-
(1S)-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]ethanol
-
-
(1S)-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]prop-2-en-1-ol
-
-
(1S)-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propan-1-ol
-
-
(1S)-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propane-1,3-diol
-
-
(1S)-2,2-dimethyl-1-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propan-1-ol
-
-
(1S)-2,2-dimethyl-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propan-1-ol
-
-
(1S)-2-chloro-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]ethanol
-
-
(1S)-2-methyl-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propan-1-ol
-
-
(2-cyclopropylethyl)phosphonic acid
IC50: 0.012 mM
(2-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]ethyl)phosphonic acid
-
-
(2E)-3-(4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl)prop-2-en-1-ol
-
-
(2E)-3-(4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl)prop-2-enoic acid
-
-
(2E)-3-cyclopropylacrylic acid
IC50: 0.003 mM
(2E)-3-cyclopropylprop-2-en-1-ol
IC50: 0.0008 mM
(2R)-3,3-dimethyl-2-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]butan-2-ol
-
-
(2S)-2-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]but-3-en-2-ol
-
-
(2S)-2-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]butan-2-ol
-
-
(2S)-2-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]pent-4-en-2-ol
-
-
(2S)-3-methyl-2-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]butan-2-ol
-
-
(2Z)-3-(4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl)prop-2-en-1-ol
-
-
(2Z)-3-(4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl)prop-2-enoic acid
-
-
(2Z)-3-cyclopropylacrylic acid
IC50: 0.003 mM
(2Z)-3-cyclopropylprop-2-en-1-ol
IC50: 0.0007 mM
(3-(dimethylamino)-1-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propyl)phosphonic acid
-
-
(3-cyclopropylpropyl)phosphonic acid
IC50: 0.032 mM
(3-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propyl)phosphonic acid
-
-
(3R)-3-hydroxy-3-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propanoic acid
-
-
(3R)-3-hydroxy-3-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propanoic acid
-
-
(3S)-3-cyclopropyl-3-hydroxypropanoic acid
IC50: 0.001 mM
(3S)-3-hydroxy-3-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propanoic acid
-
-
(3S)-3-hydroxy-3-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propanoic acid
-
-
(4-(dimethylamino)-2-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]butyl)phosphonic acid
-
-
(4aS,8aR,9aS)-9a-hydroxy-3,8a-dimethyl-5-methylidene-4a,5,6,7,8,8a,9,9a-octahydronaphtho[2,3-b]furan-2(4H)-one
i.e. atractylenolide II, one of two important efficient herbal ingredients isolated from Atractylodes macrocepha exhibits specific inhibition towards UGT2B7, with negligible influence towards other UGT isoforms
(5alpha)-17-allyl-3,14-dihydroxy-4,5-epoxymorphinan-6-one
IC50 for morphine 3-glucuronide formation: 0.412 mM (noncompetitive), IC50 for morphine 3-glucuronide formation: 0.429 mM (competitive)
(8aS)-3,8a-dimethyl-5-methylidene-4a,5,6,7,8,8a-hexahydronaphtho[2,3-b]furan-2(4H)-one
i.e. atractylenolide I, one of two important efficient herbal ingredients isolated from Atractylodes macrocephala, exhibits specific competitive inhibition towards UGT2B7, with negligible influence towards other UGT isoforms
(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulene-9-carboxylic acid
-
-
(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulene-9-carboxylic acid
-
-
(R)-7-hydroxywarfarin
-
substrate (S)-7-hydroxywarfarin, noncompetitive
(R)-8-hydroxywarfarin
-
substrate (S)-6-hydroxywarfarin, noncompetitive
(R)-chloro(cyclopropyl)methanol
IC50: 0.0002 mM
(R)-cyclopropyl(phenyl)methanol
IC50: 0.00007 mM
(R)-phenyl[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]methanol
-
-
(S)-8-hydroxywarfarin
-
substrate (R)-8-hydroxywarfarin, noncompetitive
(S)-cyclopropyl(phenyl)methanol
IC50: 0.0009 mM
(S)-phenyl[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]methanol
-
-
(S)-phenyl[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]methanol
-
-
1-(4-methyl-1,4-diazepan-1-yl)-2-(6-(trifluoromethyl)-1H-indol-3-yl)ethane-1,2-dione
selective for isoform UGT1A1. About 50% inhibition at 0.005 mM
1-cyclopropyl-2,2-dimethylpropan-1-ol
IC50: 0.0008 mM
1-naphthol O-glucuronide
inhibitory effects on different isozymes with different substrates, overview; inhibitory effects on different isozymes with different substrates, overview; inhibitory effects on different isozymes with different substrates, overview
17alpha-ethinylestradiol
strongly inhibits the formation of etoposide alcoholic glucuronide EAG2 (IC50: 0.0 42 mM) but shows very similar and moderate inhibition on etoposide phenolic glucuronide (IC50: 0.2 mM) and etoposide alcoholic glucuronide EAG1 (IC50: 0.21 mM)
17alpha-ethynylestradiol
slightly activates the 3-beta-glucuronidation of estradiol to 116% at 0.005 mM, but inhibits it at 0.1 mM by 23%, inhibits glucuronidation of 4-methylumbelliferone at all concentration of 0.1 mM
2'-OH-PCB106
-
2'-hydroxy metabolite of polychlorinated biphenyl 106, competitive inhibition
2,3,4,5-Tetrachlorophenol
substrate inhibition; substrate inhibition
2,3,4,6-tetrachlorophenol
substrate inhibition
2,3,4-Trichlorophenol
substrate inhibition; substrate inhibition; substrate inhibition; substrate inhibition
2,3,5,6-Tetrachlorophenol
substrate inhibition
2,4,5-Trichlorophenol
substrate inhibition; substrate inhibition
2,4,6-tribromophenol
competitive inhibition; competitive inhibition; competitive inhibition; noncompetitive inhibition
2,4,6-Trichlorophenol
substrate inhibition; substrate inhibition
2,4-Dichlorophenol
substrate inhibition; substrate inhibition
2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid
-
2-bromophenol
competitive inhibition; competitive inhibition
2-chlorophenol
substrate inhibition
2-cyclopropyl-N,N-dimethylethanamine
IC50: 0.005 mM
2-cyclopropylethanol
IC50: 0.0005 mM
2-hydroxy-estradiol
-
38.5% inhibition at 0.1 mM, UGT1A3
2-hydroxyestradiol
-
inhibits 4-hydroxyestradiol glucuronidation catalyzed by UGT2B7Y
2-oxo-N-(3-(2-oxopyrrolidin-1-yl)propyl)-2-(6-(trifluoromethyl)-1H-indol-3-yl)acetamide
compound resensitizes FRII cells to ribavirin treatment by about 2 times; compound resensitizes FRII cells to ribavirin treatment by about 2 times
2-phenyl-4H-benzo[h]chromen-4-one
-
-
2-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]ethanol
-
-
2-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propan-2-ol
-
-
2-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]ethanol
-
-
20(R)-ginsenoside Rg2
reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition
20(R)-ginsenoside Rg3
reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition
20(R)-ginsenoside Rh1
reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition
20(R)-ginsenoside Rh2
reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition
20(R)-protopanaxadiol
reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition
20(R)-protopanaxatriol
reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition
20(S)-ginsenoside Rg2
reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition
20(S)-ginsenoside Rg3
reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition
20(S)-ginsenoside Rh1
reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition
20(S)-ginsenoside Rh2
reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition
20(S)-protopanaxadiol
reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition
20(S)-protopanaxatriol
reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition; reversible inhibition
3'-azido-3'-deoxythymidin
slight inhibition
3,4,5-trichlorophenol
substrate inhibition; substrate inhibition
3,5-dibromophenol
competitive inhibition; competitive inhibition; competitive inhibition; competitive inhibition
3-chlorophenol
substrate inhibition
3-cyclopropylpropan-1-ol
IC50: 0.0009 mM
3-cyclopropylpropanoic acid
IC50: 0.002 mM
3-hydroxyflavone
three-dimensional QSAR-model of UGT1A1 substrate inhibition, binding structure and modelling, overview
3-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propan-1-ol
-
-
4'-OH-PCB106
-
4'-hydroxy metabolite of polychlorinated biphenyl 106, competitive inhibition
4-azido-2-hydroxybenzoic acid
inhibition of UGT1A10 catalyzed glucuronidation of 4-nitrophenol
4-Chlorophenol
substrate inhibition
4-cyclopropylbutan-1-ol
IC50: 0.003 mM
4-cyclopropylbutanoic acid
IC50: 0.016 mM
4-demethyltranilast
bilirubin glucuronosyltransferase activity, tranilast glucuronosyltransferase activity
4-hydroxyestradiol
-
inhibits 2-hydroxyestradiol glucuronidation catalyzed by UGT1A1
4-hydroxyphenanthrene
-
-
4-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]butan-1-ol
-
-
4-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]butanoic acid
-
-
4-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]butan-1-ol
-
-
4-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]butanoic acid
-
-
5-diethylaminoethylamino-8-hydroxyimidazoacridinone
-
substrate inhibition with isoform UGT1A9
5-dimethylaminopropylamino-8-hydroxytriazoloacridinone
-
substrate inhibition with isoform UGT1A9
5-hydroxytryptophol
competitive inhibition of serotonin glucuronidation
6-hydroxywarfarin
-
competitive
7-hydroxy-4-trifluoromethylcoumarin
substrate inhibition
7-hydroxywarfarin
-
competitive
acalabrutinib
exhibits weak UGT inhibition towards all tested UGT isoforms; exhibits weak UGT inhibition towards all tested UGT isoforms; exhibits weak UGT inhibition towards all tested UGT isoforms
acetaminophen
3 mM, 90% inhibition
acetone
30% and 40% inhibition of isozyme UGT2B15 at 1%, respectively; 30% and 40% inhibition of isozyme UGT2B17 at 1%, respectively
acetonitrile
50% inhibition of isozyme UGT2B15 at 1%
aflatoxin B1
competitive, binding free energy -8.19 kcal/mol; competitive, binding free energy -9.04 kcal/mol
aflatoxin G1
noncompetitive, binding free energy -9.59 kcal/mol
amentoflavone
0.1 mM, 95.3% inhibition
arctigenin
about 20% inhibition at 0.1 mM; about 35% inhibition at 0.1 mM; about 50% inhibition at 0.1 mM; about 50% inhibition at 0.1 mM; about 65% inhibition at 0.1 mM; about 80% inhibition at 0.1 mM; about 82% inhibition at 0.1 mM; about 90% inhibition at 0.1 mM; noncompetitive inhibition toward isoform UGT2B15 with more than 80% inhibition at 0.1 mM
arctiin
about 20% inhibition at 0.1 mM; about 35% inhibition at 0.1 mM; about 50% inhibition at 0.1 mM; about 50% inhibition at 0.1 mM; about 65% inhibition at 0.1 mM; about 80% inhibition at 0.1 mM; about 82% inhibition at 0.1 mM; about 85% inhibition at 0.1 mM; competitive inhibition toward isoform UGT2B15 with more than 80% inhibition at 0.1 mM
asialo-orosomucoid
-
inhibits activity with paragloboside
-
atazanavir
-
a HIV protease inhibitor, linear mixed-type inhibition mechanism, UGT1A1, inhibition of isozymes UGT1A1, 1A3, 1A4, low inhibition of isozymes UGT1A6, 1A9, and 2B7
atractylenolide I
inhibitor of isoform UGT2B7
auriculasin
-
auriculasin inhibits isoforms UGT1A6, UGT1A8, UGT1A10, and UGT2B7 completely at 0.1 mM. Isoforms UGT1A1, UGT1A3, UGT1A7, UGT1A9, UGT2B4, and UGT2B15 show about 60%, 95%, 90%, 96%, 55% and 42% residual activity at 0.1 mM auriculasin, respectively
azidothymidine
-
selective for isozyme UGT2B7
baicalein
0.1 mM, 23.7% inhibition; 0.1 mM, 35.9% inhibition
BIBF 1202
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P06133, A0A0G2JMZ5, D6RH08 about 60% residual activity at 0.05 mM; about 70% residual activity at 0.05 mM; about 75% residual activity at 0.05 mM; about 75% residual activity at 0.05 mM; about 75% residual activity at 0.05 mM; about 85% residual activity at 0.05 mM; about 85% residual activity at 0.05 mM; about 87% residual activity at 0.05 mM; about 90% residual activity at 0.05 mM; about 90% residual activity at 0.05 mM
bisphenol A
i.e. BPA, inhibits glucuronidation of serotonin and 4-methylumbelliferone
C-1748
mixed-type inhibition of isoform UGT1A9
canagliflozin
0.1 mM, 42.3% inhibition; 0.1 mM, 49.2% inhibition
-
carbamazepine
IC50 for morphine 3-glucuronide formation: 0.431 mM (mixed type inhibition), IC50 for morphine 3-glucuronide formation: 0.456 mM (mixed type inhibition)
celecoxib
significantly inhibits glucuronidation of 20-hydroxyeicosatetraenoic acid
chenodeoxycholic acid
-
inhibits glucuronidation of bilirubin
cyclopropanecarboxylic acid
IC50: 0.001 mM
dabrafenib
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P06133, A0A0G2JMZ5, D6RH08 about 10% residual activity at 0.05 mM; about 17% residual activity at 0.05 mM; about 30% residual activity at 0.05 mM; about 38% residual activity at 0.05 mM; about 40% residual activity at 0.05 mM; about 40% residual activity at 0.05 mM; about 5% residual activity at 0.05 mM; about 55% residual activity at 0.05 mM; about 59% residual activity at 0.05 mM; about 68% residual activity at 0.05 mM; about 8% residual activity at 0.05 mM; about 8% residual activity at 0.05 mM
diazepam
IC50 for morphine 3-glucuronide formation: 0.057 mM (noncompetitive), IC50 for morphine 3-glucuronide formation: 0.053 mM (noncompetitive)
dictamine
competitive, strong inhibitor; competitive, strong inhibitor; competitive, strong inhibitor; competitive, strong inhibitor
-
diethyl ((2R)-2-hydroxy-2-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]ethyl)phosphonate
-
-
diethyl ((2S)-2-hydroxy-2-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]ethyl)phosphonate
-
-
diethyl ((3R)-3-hydroxy-3-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propyl)phosphonate
-
-
diethyl ((3S)-3-hydroxy-3-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propyl)phosphonate
-
-
diethyl [(2R)-2-cyclopropyl-2-hydroxyethyl]phosphonate
IC50: 0.01 mM
diethyl [(3R)-3-cyclopropyl-3-hydroxypropyl]phosphonate
IC50: 0.005 mM
diethyl [(3S)-3-cyclopropyl-3-hydroxypropyl]phosphonate
IC50: 0.004 mM
diethyl [(R)-cyclopropyl(hydroxy)methyl]phosphonate
IC50: 0.01 mM
Digitonin
-
inhibition above 0.6 mg/mg protein; no effect at saturating substrate concentrations
dimethyl ((3R)-3-hydroxy-3-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propyl)phosphonate
-
-
dimethyl ((3S)-3-hydroxy-3-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propyl)phosphonate
-
-
dimethyl [(3R)-3-cyclopropyl-3-hydroxypropyl]phosphonate
IC50: 0.003 mM
dimethyl [(3S)-3-cyclopropyl-3-hydroxypropyl]phosphonate
IC50: 0.004 mM
emodin
inhibits tizoxanide glucuronidation activities in the human liver and even more in intestinal microsomes; inhibits tizoxanide glucuronidation activities in the human liver and even more in intestinal microsomes
ethanol
50% inhibition of isozyme UGT2B17 at 1%
ethyl (3R)-3-hydroxy-3-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propanoate
-
-
ethyl (3R)-3-hydroxy-3-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propanoate
-
-
ethyl (3S)-3-cyclopropyl-3-hydroxypropanoate
IC50: 0.0003 mM
ethyl (3S)-3-hydroxy-3-[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propanoate
-
-
ethyl (3S)-3-hydroxy-3-[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]propanoate
-
-
eugenol
-
UGT2B7, 54.5% inhibition at 0.1 mM
Flufenamic acid
0.02-0.5 mM, completely inhibits glucuronidation of 4-methylumbelliferone; 0.02-0.5 mM, inhibits glucuronidation of 4-methylumbelliferone
flunitrazepam
-
competitive inhibition of estrogen and buprenorphine catalyzed by UGT1A1 and UGT2B7Y, not inhibition of UGT1A3
galangin
0.1 mM, 88.5% inhibition; 0.1 mM, 93.6% inhibition; 0.1 mM, 94.8% inhibition; 0.1 mM, 98.7% inhibition
gamma-fagarine
competitive, strong inhibitor; competitive, strong inhibitor; competitive, strong inhibitor; competitive, strong inhibitor
-
gemfibrozil
-
inhibits both UGT and CYP2C8, about 50% inhibition via a non-specific, competitive process in drug distribution to UGT
genistein
0.003 mM, 25.4% inhibition. 0.03 mM, 79.5% inhibition; 0.003 mM, 38.8% inhibition. 0.03 mM, 97.6% inhibition; weak; weak
gomisin J
inhibitor of isoform UGT1A9
gossypol
-
noncompetitive inhibitin of estradiol-3-glucuronidation and propofol O-glucuronidation, competitive inhibition towards 3'-azido-3'-deoxythymidine glucuronidation
haplopine
competitive, strong inhibitor; competitive, strong inhibitor; competitive, strong inhibitor; competitive, strong inhibitor
-
Ibuprofen
significantly inhibits glucuronidation of 20-hydroxyeicosatetraenoic acid
indinavir
-
a HIV protease inhibitor, linear mixed-type inhibition mechanism, UGT1A1, inhibition of isozymes UGT1A1, 1A3, 1A4, low inhibition of isozymes UGT1A6, 1A9, and 2B7
indomethacin
significantly inhibits glucuronidation of 20-hydroxyeicosatetraenoic acid
lacto-N-biose
-
22% inhibition of recombinant GlcAT-P and 77.3% of recombinant GlcAT-S at 5 mM
lactose
-
24.5% inhibition of recombinant GlcAT-S at 5 mM, no inhibition of recombinant GlcAT-P
lamotrigen
-
low-affinity substrate of isoform UGT1A4, noncompetitively inhibits dihydrotestosterone and trans-androsterone glucuronidation
long-chain unsaturated fatty acids
selective inhibition of some UGT isozymes
-
longifolol
-
and derivatives of primary alcohol series or carboxylic/phosphonic acids and amines, inhibitory potency, overview
lopinavir
-
a HIV protease inhibitor, inhibition of isozymes UGT1A1, 1A3, 1A4, low inhibition of isozymes UGT1A6, 1A9, and 2B7
lorazepam
IC50 for morphine 3-glucuronide formation: 0.065 mM (mixed type inhibition), IC50 for morphine 3-glucuronide formation: 0.056 mM (mixed type inhibition)
magnolol
combined treatment decreases IC50 values for 2,4-dibromophenol and vice versa. The 2 inhibitors and UGT1A9 can form a ternary complex
monobenzyl phthalate
-
isoform UGT1A9 shows 92.49% inhibition at 0.1 mM
monocyclohexyl phthalate
-
isoform UGT1A9 shows 95.9% inhibition at 0.1 mM
monoethylhexyl phthalate
-
isoform UGT1A7 shows 85.26% inhibition at 0.1 mM, isoform UGT1A9 shows 97.61% inhibition at 0.1 mM
monohexyl phthalate
-
isoform UGT1A9 shows 85.83% inhibition at 0.1 mM
monooctyl phthalate
-
isoform UGT1A9 shows 91.21% inhibition at 0.1 mM
morin
0.1 mM, 81.6% inhibition; 0.1 mM, 89.2% inhibition; 0.1 mM, 96.1% inhibition; 0.1 mM, 96.8% inhibition
mycophenolate
IC50 for morphine 3-glucuronide formation: 0.341 mM (noncompetitive), IC50 for morphine 3-glucuronide formation: 0.389 mM (noncompetitive)
myricetin
competitive; mixed type; non-competitive; non-competitive; non-competitive; non-competitive; non-competitive
N-(2-((dimethylamino)methyl)benzyl)-2-oxo-2-(6-(trifluoromethyl)-1H-indol-3-yl)acetamide
0.005 mM, 80% inhibition. Kd value 0.0337 mM. Compound resensitizes FRII cells to ribavirin treatment by about 2 times; compound resensitizes FRII cells to ribavirin treatment by about 2 times
N-(3-(dimethylamino)propyl)-N-methyl-2-oxo-2-(6-(trifluoromethyl)-1H-indol-3-yl)acetamide
compound resensitizes FRII cells to ribavirin treatment by about 2 times; compound resensitizes FRII cells to ribavirin treatment by about 2 times
N-acetyllactosamine
-
87.4% inhibition of recombinant GlcAT-P and 83.7% of recombinant GlcAT-S at 5 mM
naphthol
-
UGT1A6, 87.0% inhibition at 0.05 mM
naproxen
significantly inhibits glucuronidation of 20-hydroxyeicosatetraenoic acid
nelfinavir
-
a HIV protease inhibitor, inhibition of isozymes UGT1A1, 1A3, 1A4, low inhibition of isozymes UGT1A6, 1A9, and 2B7
nintedanib
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P06133, A0A0G2JMZ5, D6RH08 about 1% residual activity at 0.05 mM; about 10% residual activity at 0.05 mM; about 15% residual activity at 0.05 mM; about 18% residual activity at 0.05 mM; about 25% residual activity at 0.05 mM; about 3% residual activity at 0.05 mM; about 38% residual activity at 0.05 mM; about 40% residual activity at 0.05 mM; about 5% residual activity at 0.05 mM; about 5% residual activity at 0.05 mM
niotinib
a selective inhibitor of UGT1A1
-
nordihydroguaiaretic acid
-
opicabone
IC50 values increase at higher substrate concentrations; IC50 values increase at higher substrate concentrations; IC50 values increase at higher substrate concentrations; IC50 values increase at higher substrate concentrations; IC50 values increase at higher substrate concentrations
-
oxazepam
IC50 for morphine 3-glucuronide formation: 0.109 mM (competitive), IC50 for morphine 3-glucuronide formation: 0.119 mM (mixed type inhibition)
p-[di-n-Propylsulfamoyl]benzoic acid
-
i.e. probenecid
Pentachlorophenol
substrate inhibition
protopanaxadiol
-
competitive inhibition
ritonavir
-
a HIV protease inhibitor, inhibition of isozymes UGT1A1, 1A3, 1A4, low inhibition of isozymes UGT1A6, 1A9, and 2B7
salvigenin
0.1 mM, 55.2% inhibition; 0.1 mM, 60% inhibition
-
saquinavir
-
a HIV protease inhibitor, inhibition of isozymes UGT1A1, 1A3, 1A4, low inhibition of isozymes UGT1A6, 1A9, and 2B7
sauchinone
noncompetitive inhibition; noncompetitive inhibition
schisandrin A
inhibitor of isoform UGT1A1; inhibitor of isoform UGT1A3
skimmianine
competitive, strong inhibitor; competitive, strong inhibitor; competitive, strong inhibitor; competitive, strong inhibitor
-
sulfinpyrazone
-
a UGT1A selective inhibitor
tacrolimus
IC50 for morphine 3-glucuronide formation: 0.384 mM (mixed type inhibition), IC50 for morphine 3-glucuronide formation: 0.488 mM (mixed type inhibition)
trametinib
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P06133, A0A0G2JMZ5, D6RH08 about 10% residual activity at 0.05 mM; about 2% residual activity at 0.05 mM; about 25% residual activity at 0.05 mM; about 25% residual activity at 0.05 mM; about 25% residual activity at 0.05 mM; about 30% residual activity at 0.05 mM; about 45% residual activity at 0.05 mM; about 45% residual activity at 0.05 mM; about 5% residual activity at 0.05 mM; about 6% residual activity at 0.05 mM; about 60% residual activity at 0.05 mM; about 85% residual activity at 0.05 mM
tranilast
bilirubin glucuronosyltransferase activity, activity in human jejunum microsomes is strongly inhibited (0.0753 mM)
trans-androsterone
-
uncompetitive substrate inhibition
Triphenylacetic acid
-
competitive to bilirubin
troglitazone
-
inhibition of bilirubin glucuronidation by UGT1A1
UDP-glucose
competitive inhibition, predicted binding sites in isozyme UGT1A10 are sites N292, K314, K315, and K404, overview
UDP-hexanol amine
competitive inhibition, predicted binding sites in isozyme UGT1A10 are sites N292, K314, K315, and K404
wogonin
0.1 mM, 38.4% inhibition; 0.1 mM, 38.8% inhibition
xanthotoxol
substrate inhibition of isoform UGT1A1; substrate inhibition of isoform UGT1A10; substrate inhibition of isoform UGT1A8
[(1E)-3-(4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl)prop-1-en-1-yl]phosphonic acid
-
-
[(1E)-3-cyclopropylprop-1-en-1-yl]phosphonic acid
IC50: 0.041 mM
[(2R)-2-cyclopropyl-2-hydroxyethyl]phosphonic acid
IC50: 0.013 mM
[(3R)-3-cyclopropyl-3-hydroxypropyl]phosphonic acid
IC50: 0.028 mM
[(3S)-3-cyclopropyl-3-hydroxypropyl]phosphonic acid
IC50: 0.018 mM
[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]acetic acid
-
-
[(9R)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]methanol
-
-
[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]acetic acid
-
-
[(9S)-4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl]methanol
-
-
[(E)-2-(4,8,8-trimethyldecahydro-1,4-methanoazulen-9-yl)ethenyl]phosphonic acid
-
-
[(E)-2-cyclopropylvinyl]phosphonic acid
IC50: 0.008 mM
[(R)-cyclopropyl(hydroxy)methyl]phosphonic acid
IC50: 0.018 mM
1-naphthol

substrate inhibition; substrate inhibition; substrate inhibition; substrate inhibition; substrate inhibition; substrate inhibition; substrate inhibition; substrate inhibition; substrate inhibition; substrate inhibition
1-naphthol
inhibitory effects on different isozymes with different substrates, overview; inhibitory effects on different isozymes with different substrates, overview; inhibitory effects on different isozymes with different substrates, overview
2,4-Dibromophenol

competitive inhibition; competitive inhibition; competitive inhibition; competitive inhibition
2,4-Dibromophenol
combined treatment decreases IC50 values for magnolol and vice versa. The 2 inhibitors and UGT1A9 can form a ternary complex
2,5-dibromophenol

competitive inhibition; competitive inhibition; competitive inhibition; competitive inhibition
4-Methylumbelliferone

substrate inhibition; substrate inhibition; substrate inhibition; substrate inhibition; substrate inhibition; substrate inhibition; substrate inhibition; substrate inhibition; substrate inhibition; substrate inhibition
4-Methylumbelliferone
-
substrate inhibition
4-nitrophenol

-
uncompetitive to chenodeoxycholic acid
4-nitrophenol
inhibits the etoposide glucuronosyltransferase activity in liver microsomes
4-nitrophenol
-
competitive
amitriptyline

IC50 for morphine 3-glucuronide formation: 0.159 mM (noncompetitive), IC50 for morphine 3-glucuronide formation: 0.136 mM (mixed type inhibition)
amitriptyline
substrate inhibition
androsterone

-
inhibition of glucuronidation of troglitazone catalyzed by isozymes of UGT2 family
androsterone
inhibits protocatechuic aldehyde glucuronidation by isozyme UGT1A9 and slightly by liver microsomes
beta-estradiol

completely inhibits the etoposide glucuronosyltransferase activity in liver microsomes at 0.5 mM
beta-estradiol
-
61.5% inhibition at 0.2 mM, UGT1A1
beta-estradiol
exhibits strong inhibition on etoposide phenolic glucuronide (IC50: 0.068 mM) and etoposide alcoholic glucuronide EAG2 (IC50: 0.086 mM). The inhibitory effect of beta-estradiol on the formation of etoposide alcoholic glucuronide EAG1 is not so significant in comparison with the other two etoposide glucuronide isomers, even at very high concentration of beta-estradiol (about 80% at 2 mM)
beta-phenyllongifolol

highly selective for isozyme UGT2B7, the mode of inhibition is rapidly reversible and competitive, inhibitor is not glucuronidated by UGT2B7 or other hepatic UGTs
beta-phenyllongifolol
specific for isozyme UGT2B7
bilirubin

-
competitive to chenodeoxycholic acid
bilirubin
completely inhibits the etoposide glucuronosyltransferase activity in liver microsomes at 0.5 mM
bilirubin
specific for isozyme UGT1A1, strong inhibition of sitafloxacin and moxifloxacin glucuronidation, moderate inhibition of levofloxacin glucuronidation, and weak inhibition of grepafloxacin glucuronidation
bilirubin
strongly inhibits the formation of etoposide phenolic glucuronide (IC50: 0.075 mM) and EAG1 (I50: 0.054 mM), and significantly inhibits the formation of etoposide alcoholic glucuronide EAG2 (IC50: 0.140 mM)
bilirubin
tranilast glucuronosyltransferase activity, activity in human jejunum microsomes is strongly inhibited (IC50: 0.0811 mM)
bilirubin
0.1 mM, 95.7% inhibition. 0.003 mM, 64.7% inhibition; 0.1 mM, very weak inhibition; very weak inhibition
bilirubin
three-dimensional QSAR-model of UGT1A1 substrate inhibition, binding structure and modelling, overview
bilirubin
very low inhibition
clomipramine

IC50 for morphine 3-glucuronide formation: 0.04 mM (noncompetitive), IC50 for morphine 3-glucuronide formation: 0.037 mM (mixed type inhibition)
curcumin

-
curcumin
-
reversable by low glucuronidation activity with curcumin as substrate, overview
desipramine

-
diclofenac

-
inhibits the in vitro glucuronidation of morphine and codeine by liver microsomes
diclofenac
inhibition of denopamine glucuroniation
diclofenac
0.01 mM, 40.6% inhibition. 0.03 mM, 67% inhibition; very weak inhibition; weak; weak
diclofenac
IC50 for morphine 3-glucuronide formation: 0.032 mM (noncompetitive), IC50 for morphine 3-glucuronide formation: 0.031 mM (noncompetitive)
diclofenac
high inhibition
diclofenac
significantly inhibits glucuronidation of 20-hydroxyeicosatetraenoic acid, competitive inhibition. Diclofenac decreases 20-hydroxyeicosatetraenoic acid glucuronidation in human liver microsomes carrying UGT2B7*2 alleles
DMSO

50% inhibition of isozyme UGT2B17 at 0.5%
DMSO
2% v/v reduces enzyme activity in liver microsomes; 2% v/v reduces enzyme activity in liver microsomes; 2% v/v reduces enzyme activity in liver microsomes; 2% v/v reduces enzyme activity in liver microsomes; 2% v/v reduces enzyme activity in liver microsomes; 2% v/v reduces enzyme activity in liver microsomes; 2% v/v reduces enzyme activity in liver microsomes; 2% v/v reduces enzyme activity in liver microsomes; 2% v/v reduces enzyme activity in liver microsomes; 2% v/v reduces enzyme activity in liver microsomes; 2% v/v reduces enzyme activity in liver microsomes
efavirenz

-
estradiol

-
competitive to chenodeoxycholic acid
estradiol
inhibits tizoxanide glucuronidation activities in the human liver and intestinal microsomes; inhibits tizoxanide glucuronidation activities in the human liver and intestinal microsomes
fluconazole

2.5 mM, 0.075 mM naproxen, 72% inhibition
fluconazole
-
a UGT2B7 selective inhibitor
fluconazole
a UGT2B7 selective inhibitor
fluconazole
high inhibition
hecogenin

-
48.0% inhibition at 0.05 mM, UGT1A4
hecogenin
a selective UGT1A4 inhibitor, complete inhibition of UGT1A4 at 0.05 mM
hecogenin
-
noncompetitive inhibition of senecionine glucuronidation, more than 80% inhibition at 0.2 mM
ibrutinib

P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P06133, A0A0G2JMZ5, D6RH08 about 12% residual activity at 0.05 mM; about 12% residual activity at 0.05 mM; about 12% residual activity at 0.05 mM; about 2% residual activity at 0.05 mM; about 20% residual activity at 0.05 mM; about 20% residual activity at 0.05 mM; about 20% residual activity at 0.05 mM; about 25% residual activity at 0.05 mM; about 5% residual activity at 0.05 mM; about 5% residual activity at 0.05 mM; about 50% residual activity at 0.05 mM
ibrutinib
competitive inhibition against UGT1A1, exerts broad inhibition on most UGTs; competitive inhibition against UGT1A1, exerts broad inhibition on most UGTs; competitive inhibition against UGT1A1, exerts broad inhibition on most UGTs
imipramine

inhibits the etoposide glucuronosyltransferase activity in liver microsomes
imipramine
IC50 for morphine 3-glucuronide formation: 0.129 mM (noncompetitive), IC50 for morphine 3-glucuronide formation: 0.116 mM (mixed type inhibition)
imipramine
substrate inhibition
isolongifolol

IC50: 0.0001 mM
isolongifolol
-
and derivatives of primary alcohol series or carboxylic/phosphonic acids and amines, inhibitory potency, overview
kaempferol

the formation of ethylglucuronoside is inhibited by the flavonoids for all UGT enzymes except for UGT2B15, mechanism-based inhibition; the formation of ethylglucuronoside is inhibited by the flavonoids for all UGT enzymes except for UGT2B15, mechanism-based inhibition; the formation of ethylglucuronoside is inhibited by the flavonoids for all UGT enzymes except for UGT2B15, mechanism-based inhibition; the formation of ethylglucuronoside is inhibited by the flavonoids for all UGT enzymes except for UGT2B15, mechanism-based inhibition; the formation of ethylglucuronoside is inhibited by the flavonoids for all UGT enzymes except for UGT2B15, mechanism-based inhibition; the formation of ethylglucuronoside is inhibited by the flavonoids for all UGT enzymes except for UGT2B15, mechanism-based inhibition; the formation of ethylglucuronoside is inhibited by the flavonoids for all enzymes except for UGT2B15, mechanism-based inhibition
kaempferol
0.1 mM, 96.5% inhibition
ketoconazole

-
-
Mefenamic acid

specific for isozyme UGT1A9, strong inhibition of grepafloxacin glucuronidation, weak inhibition of levofloxacin, sitafloxacin and moxifloxacin glucuronidation
Mefenamic acid
0.02-0.5 mM, completely inhibits glucuronidation of 4-methylumbelliferone; 0.02-0.5 mM, inhibits glucuronidation of 4-methylumbelliferone
Mefenamic acid
almoste complete inhibition
Mefenamic acid
significantly inhibits glucuronidation of 20-hydroxyeicosatetraenoic acid
morphine

inhibits the etoposide glucuronosyltransferase activity in liver microsomes
morphine
three-dimensional QSAR-model of UGT1A1 substrate inhibition, binding structure and modelling, overview
niflumic acid

0.02-0.5 mM, 66% inhibition of glucuronidation of 4-methylumbelliferone; 0.02-0.5 mM, inhibits glucuronidation of 4-methylumbelliferone
niflumic acid
0.01 mM, 90.7% inhibition
olanzapine

IC50 for morphine 3-glucuronide formation: 0.368 mM (noncompetitive), IC50 for morphine 3-glucuronide formation: 0.4 mM (mixed type inhibition)
Phenylbutazone

above 1 mM
Phenylbutazone
-
a UGT1A selective inhibitor
Phenylbutazone
inhibits protocatechuic aldehyde glucuronidation by isozyme UGT1A6 and liver microsomes
Phenylbutazone
very low inhibition
propofol

-
UGT1A9, 37.0% inhibition at 0.05 mM
propofol
0.03 mM, weak inhibition; 0.1 mM, weak; weak inhibition at 0.03 mM, moderate inhibition at 0.1 mM
propofol
inhibits 3-beta-glucuronidation of estradiol by recombinant isozyme UGT1A1 and by liver microsomes
quercetin

the formation of ethylglucuronoside is inhibited by the flavonoids for all UGT enzymes except for UGT2B15, mechanism-based inhibition; the formation of ethylglucuronoside is inhibited by the flavonoids for all UGT enzymes except for UGT2B15, mechanism-based inhibition; the formation of ethylglucuronoside is inhibited by the flavonoids for all UGT enzymes except for UGT2B15, mechanism-based inhibition; the formation of ethylglucuronoside is inhibited by the flavonoids for all UGT enzymes except for UGT2B15, mechanism-based inhibition; the formation of ethylglucuronoside is inhibited by the flavonoids for all UGT enzymes except for UGT2B15, mechanism-based inhibition; the formation of ethylglucuronoside is inhibited by the flavonoids for all UGT enzymes except for UGT2B15, mechanism-based inhibition; the formation of ethylglucuronoside is inhibited by the flavonoids for all enzymes except for UGT2B15, mechanism-based inhibition
quercetin
0.1 mM, 88.3% inhibition; 0.1 mM, 91% inhibition; 0.1 mM, 96.1% inhibition
tamoxifen

IC50 for morphine 3-glucuronide formation: 0.093 mM (noncompetitive), IC50 for morphine 3-glucuronide formation: 0.107 mM (noncompetitive)
tamoxifen
-
uncompetitive substrate inhibition. Coincubation with tamoxifen, a high-affinity substrate of isoform UGT1A4, results in a concentration-dependent activation/inhibition effect on dihydrotestosterone and trans-androsterone glucuronidation
testosterone

-
noncompetitive to chenodeoxycholic acid
testosterone
-
inhibition of glucuronidation of troglitazone catalyzed by isozymes of UGT2 family, other 8 steroids tested on hUGT2A1
Triton X-100

-
above 0.01% v/v; no effect at saturating substrate concentrations
Triton X-100
-
inhibition of UGT2B and almost all of the UGT1A isozymes, not inhibit glucuronidation of 1-naphthol nor scopoletin by UGT1A9, inhibition of entacapone glucuronidation tested on isozymes of UGT1A and UGT1B families, only for UGT1A9 showed reversible inhibition
Triton X-100
inhibition of recombinant soluble isozyme UGT1A9
UDP

strongly inhibits isozymes UGT1A1 and UGT1A4 in a competitive manner for the 5'-diphosphoglucuronic acid binding; strongly inhibits isozymes UGT1A1 and UGT1A4 in a competitive manner for the 5'-diphosphoglucuronic acid binding; strongly inhibits isozymes UGT1A1 and UGT1A4 in a competitive manner for the 5'-diphosphoglucuronic acid binding
additional information

-
norepinephrine does not inhibit UGT2B7Y, UGT1A1 nor UGT1A3
-
additional information
-
acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview
-
additional information
acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview
-
additional information
acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview
-
additional information
acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview
-
additional information
acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview
-
additional information
acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview
-
additional information
acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview
-
additional information
acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview
-
additional information
acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview
-
additional information
acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview; acetone, acetonitrile, dimethyl sulfoxide, ethanol, and methanol have only little inhibitory effect on the isozyme, overview
-
additional information
-
no effect by 1% v/v DMSO and 2% v/v methanol on denopamine glucuronidation
-
additional information
no effect by 1% v/v DMSO and 2% v/v methanol on denopamine glucuronidation
-
additional information
no effect by 1% v/v DMSO and 2% v/v methanol on denopamine glucuronidation
-
additional information
no effect by 1% v/v DMSO and 2% v/v methanol on denopamine glucuronidation
-
additional information
no effect by 1% v/v DMSO and 2% v/v methanol on denopamine glucuronidation
-
additional information
no effect by 1% v/v DMSO and 2% v/v methanol on denopamine glucuronidation
-
additional information
no effect by 1% v/v DMSO and 2% v/v methanol on denopamine glucuronidation
-
additional information
no effect by 1% v/v DMSO and 2% v/v methanol on denopamine glucuronidation
-
additional information
no effect by 1% v/v DMSO and 2% v/v methanol on denopamine glucuronidation
-
additional information
no effect by 1% v/v DMSO and 2% v/v methanol on denopamine glucuronidation
-
additional information
no effect by 1% v/v DMSO and 2% v/v methanol on denopamine glucuronidation
-
additional information
-
IC50 values for HIV protease inhibitors with UGT isozymes, overview
-
additional information
-
detailed structure-activity relationships, the glucuronidation of substrate compounds is prevented by the introduction of bulky substituents such as isopropyl, tert-butyl, and phenyl groups, overview
-
additional information
design of UGT inhibitors based on rational principles such as detailed structure-activity relationships, synthesis of twenty-four homochiral and epimeric longifolol derivatives and screening for UGT2B7 inhibitory potency, determination of the absolute configuration at the stereogenic center C1' by X-ray crystallography and 2D NMR spectroscopy, gHSQC, gNOESY, stereochemistry, overview, substrate-dependent and substrate-independent inhibition, overview
-
additional information
-
design of UGT inhibitors based on rational principles such as detailed structure-activity relationships, synthesis of twenty-four homochiral and epimeric longifolol derivatives and screening for UGT2B7 inhibitory potency, determination of the absolute configuration at the stereogenic center C1' by X-ray crystallography and 2D NMR spectroscopy, gHSQC, gNOESY, stereochemistry, overview, substrate-dependent and substrate-independent inhibition, overview
-
additional information
isozyme UGT1A6 is more sensitive to detergent inhibition as isozyme UGT1A9; isozyme UGT1A6 is more sensitive to detergent inhibition as isozyme UGT1A9
-
additional information
isozyme UGT1A6 is more sensitive to detergent inhibition as isozyme UGT1A9; isozyme UGT1A6 is more sensitive to detergent inhibition as isozyme UGT1A9
-
additional information
isozyme UGT1A6 is more sensitive to detergent inhibition as isozyme UGT1A9; isozyme UGT1A6 is more sensitive to detergent inhibition as isozyme UGT1A9
-
additional information
isozyme UGT1A6 is more sensitive to detergent inhibition as isozyme UGT1A9; isozyme UGT1A6 is more sensitive to detergent inhibition as isozyme UGT1A9
-
additional information
-
1-naphthol, 2-naphthol, 4-nitrophenol, and 4-methylumbelliferone with high turnover rates show more potent inhibition of the activity in human liver microsomes compared with that by the recombinant UGT1A1, inhibitory effects of UDP on UGT, overview; 1-naphthol, 2-naphthol, 4-nitrophenol, and 4-methylumbelliferone with high turnover rates show more potent inhibition of the activity in human liver microsomes, inhibitory effects of UDP on UGT, overview; 1-naphthol, 2-naphthol, 4-nitrophenol, and 4-methylumbelliferone with high turnover rates show more potent inhibition of the activity in human liver microsomes, inhibitory effects of UDP on UGT, overview
-
additional information
1-naphthol, 2-naphthol, 4-nitrophenol, and 4-methylumbelliferone with high turnover rates show more potent inhibition of the activity in human liver microsomes compared with that by the recombinant UGT1A1, inhibitory effects of UDP on UGT, overview; 1-naphthol, 2-naphthol, 4-nitrophenol, and 4-methylumbelliferone with high turnover rates show more potent inhibition of the activity in human liver microsomes, inhibitory effects of UDP on UGT, overview; 1-naphthol, 2-naphthol, 4-nitrophenol, and 4-methylumbelliferone with high turnover rates show more potent inhibition of the activity in human liver microsomes, inhibitory effects of UDP on UGT, overview
-
additional information
1-naphthol, 2-naphthol, 4-nitrophenol, and 4-methylumbelliferone with high turnover rates show more potent inhibition of the activity in human liver microsomes compared with that by the recombinant UGT1A1, inhibitory effects of UDP on UGT, overview; 1-naphthol, 2-naphthol, 4-nitrophenol, and 4-methylumbelliferone with high turnover rates show more potent inhibition of the activity in human liver microsomes, inhibitory effects of UDP on UGT, overview; 1-naphthol, 2-naphthol, 4-nitrophenol, and 4-methylumbelliferone with high turnover rates show more potent inhibition of the activity in human liver microsomes, inhibitory effects of UDP on UGT, overview
-
additional information
-
inhibition of UGT activity by PKCepsilon-specific antagonist peptide or by PKCapsilon-targeted destruction with PKCepsilon-specific small interference RNA and activation of curcumin-down-regulated UGTs with typical PKC agonists verify a central PKC role in glucuronidation, overview. UGT down-regulation by the tyrosine kinase-specific inhibitor, herbimycin-A, suggests cellular oxidant-/H2O2-activated PKC via tyrosine phosphorylation also plays a role in sustaining UGT activity
-
additional information
the formation of ethylglucuronoside is inhibited by the flavonoids kaempferol and quercetin for all enzymes except for UGT2B15, mechanism-based inhibition
-
additional information
the formation of ethylglucuronoside is inhibited by the flavonoids kaempferol and quercetin for all enzymes except for UGT2B15, mechanism-based inhibition
-
additional information
the formation of ethylglucuronoside is inhibited by the flavonoids kaempferol and quercetin for all enzymes except for UGT2B15, mechanism-based inhibition
-
additional information
the formation of ethylglucuronoside is inhibited by the flavonoids kaempferol and quercetin for all enzymes except for UGT2B15, mechanism-based inhibition
-
additional information
the formation of ethylglucuronoside is inhibited by the flavonoids kaempferol and quercetin for all enzymes except for UGT2B15, mechanism-based inhibition
-
additional information
the formation of ethylglucuronoside is inhibited by the flavonoids kaempferol and quercetin for all enzymes except for UGT2B15, mechanism-based inhibition
-
additional information
the formation of ethylglucuronoside is inhibited by the flavonoids kaempferol and quercetin for all enzymes except for UGT2B15, mechanism-based inhibition
-
additional information
the formation of ethylglucuronoside is inhibited by the flavonoids kaempferol and quercetin for all enzymes except for UGT2B15, mechanism-based inhibition
-
additional information
-
the formation of ethylglucuronoside is inhibited by the flavonoids kaempferol and quercetin for all enzymes except for UGT2B15, mechanism-based inhibition
-
additional information
no inhibition by hecogenin; no inhibition by hecogenin; no inhibition by nicotine
-
additional information
no inhibition by hecogenin; no inhibition by hecogenin; no inhibition by nicotine
-
additional information
no inhibition by hecogenin; no inhibition by hecogenin; no inhibition by nicotine
-
additional information
-
no inhibition by hecogenin; no inhibition by hecogenin; no inhibition by nicotine
-
additional information
the majority of antidepressant and antipsychotic drugs screened for effects on UGT2B10 inhibit the enzyme activity with IC50 values below 0.1 mM. The most potent inhibition is observed with the tricyclic antidepressants amitriptyline and doxepin and the tetracyclic antidepressant mianserin, and the structurally related compounds desloratadine and loratadine. Molecular modeling using a ligand-based approach indicates that hydrophobic and charge interactions are involved in inhibitor binding, whereas spatial features influence the potency of UGT2B10 inhibition. UGT enzyme-selective inhibitor screening, overview
-
additional information
-
the majority of antidepressant and antipsychotic drugs screened for effects on UGT2B10 inhibit the enzyme activity with IC50 values below 0.1 mM. The most potent inhibition is observed with the tricyclic antidepressants amitriptyline and doxepin and the tetracyclic antidepressant mianserin, and the structurally related compounds desloratadine and loratadine. Molecular modeling using a ligand-based approach indicates that hydrophobic and charge interactions are involved in inhibitor binding, whereas spatial features influence the potency of UGT2B10 inhibition. UGT enzyme-selective inhibitor screening, overview
-
additional information
in silico docking and molecular homology modeling for inhibition mechanism elucidation. Atractylenolide I exerts stronger inhibition potential than atractylenolide III towards UGT2B7, which is attributed to the different hydrogen bonds and hydrophobic interactions. Inhibition kinetic analysis for the inhibition of atractylenolide I towards UGT2B7 reveals competitive inhibition by atractylenolide I
-
additional information
-
isoforms UGT2B4, UGT2B7, UGT2B15 and UGT2B17 are not inhibited by lapatinib. Isoforms UGT2B4 and UGT2B17 are not inhibited by pazopanib. Isoforms UGT2B4 and UGT2B15 are not inhibited by regorafenib
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additional information
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0.1 mM phthalate monoesters exhibit weak inhibition towards isoforms UGT1A10, UGT2B4, UGT2B7, UGT2B15 and UGT2B17 by reducing the glucuronidation less than 80%
-
additional information
not inhibited by 2,4-dibromophenol, 2,5-dibromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol; not inhibited by 2-bromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol and 2,4-dibromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 2,5-dibromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 2,5-dibromophenol and 3,5-dibromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 3,5-dibromophenol and 2,4,6-tribromophenol
-
additional information
not inhibited by 2,4-dibromophenol, 2,5-dibromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol; not inhibited by 2-bromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol and 2,4-dibromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 2,5-dibromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 2,5-dibromophenol and 3,5-dibromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 3,5-dibromophenol and 2,4,6-tribromophenol
-
additional information
not inhibited by 2,4-dibromophenol, 2,5-dibromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol; not inhibited by 2-bromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol and 2,4-dibromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 2,5-dibromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 2,5-dibromophenol and 3,5-dibromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 3,5-dibromophenol and 2,4,6-tribromophenol
-
additional information
not inhibited by 2,4-dibromophenol, 2,5-dibromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol; not inhibited by 2-bromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol and 2,4-dibromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 2,5-dibromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 2,5-dibromophenol and 3,5-dibromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 3,5-dibromophenol and 2,4,6-tribromophenol
-
additional information
not inhibited by 2,4-dibromophenol, 2,5-dibromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol; not inhibited by 2-bromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol and 2,4-dibromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 2,5-dibromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 2,5-dibromophenol and 3,5-dibromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 3,5-dibromophenol and 2,4,6-tribromophenol
-
additional information
not inhibited by 2,4-dibromophenol, 2,5-dibromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol; not inhibited by 2-bromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol and 2,4-dibromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 2,5-dibromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 2,5-dibromophenol and 3,5-dibromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 3,5-dibromophenol and 2,4,6-tribromophenol
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additional information
not inhibited by 2,4-dibromophenol, 2,5-dibromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol; not inhibited by 2-bromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol and 2,4-dibromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 2,5-dibromophenol and 2,4,6-tribromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 2,5-dibromophenol and 3,5-dibromophenol; not inhibited by 2-bromophenol, 2,4-dibromophenol, 3,5-dibromophenol and 2,4,6-tribromophenol
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additional information
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not inhibited by glabridin, liquiritigenin, licochalcone A, isoliquiritin, astragaloside IV, alisol A, ergosterol, ginsenoside Rb1, E-arasone, saikosaponin A, linarin, luteolin, luteolin-7-O-glucoside, perilaldehyde, beta-eudesmol, apigenin 7-O-glucoside, betulinic acid, and oleanolic acid
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additional information
minimally affecting inhibitors: acetaminophen, amentoflavone
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additional information
minimally affecting inhibitors: acetaminophen, amentoflavone
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6-phosphofructokinase deficiency
Phosphofructokinase deficiency (Tarui disease) associated with hepatic glucuronyltransferase deficiency (Gilbert's syndrome): a case and family study.
Acquired Immunodeficiency Syndrome
Cost-effectiveness analysis of UGT1A1 genetic testing to inform antiretroviral prescribing in HIV disease.
Acquired Immunodeficiency Syndrome
Impact of UGT1A1 Gilbert variant on discontinuation of ritonavir-boosted atazanavir in AIDS Clinical Trials Group Study A5202.
Acute Coronary Syndrome
Study of the Association of PEAR1, P2Y12, and UGT2A1 Polymorphisms with Platelet Reactivity in Response to Dual Antiplatelet Therapy in Chinese Patients.
Adenocarcinoma
Clinical significance of UGT1A1 polymorphism and expression of ERCC1, BRCA1, TYMS, RRM1, TUBB3, STMN1 and TOP2A in gastric cancer.
Adenocarcinoma
Evaluation of the Association of Perioperative UGT1A1 Genotype-Dosed gFOLFIRINOX With Margin-Negative Resection Rates and Pathologic Response Grades Among Patients With Locally Advanced Gastroesophageal Adenocarcinoma: A Phase 2 Clinical Trial.
Adenocarcinoma
Expression of glutathione S-transferase and phenol sulfotransferase, but not of UDP-glucuronosyltransferase, in the human lung tumor cell lines NCI-H322 and NCI-H358.
Adenocarcinoma
Expression of UDP-glucuronosyltransferase 1A, nuclear factor erythroid-E2-related factor 2 and Kelch-like ECH-associated protein 1 in colonic mucosa, adenoma and adenocarcinoma tissue.
Adenocarcinoma
Glycoside conjugation in microsomes from hepatic and renal carcinoma of man.
Adenocarcinoma
Multicenter, Randomized, Phase III Trial of Neoadjuvant Chemoradiation With Capecitabine and Irinotecan Guided by UGT1A1 Status in Patients With Locally Advanced Rectal Cancer.
Adenocarcinoma
Polymorphic expression of the UDP-glucuronosyltransferase UGT1A gene locus in human gastric epithelium.
Adenocarcinoma
Polymorphisms of UDP-glucuronosyltransferase 1A7 are not involved in pancreatic diseases.
Adenocarcinoma
Prognosis genes in gastric adenocarcinoma identified by cross talk genes in disease?related pathways.
Adenocarcinoma
UGT2B17 and miR-224 contribute to hormone dependency trends in adenocarcinoma and squamous cell carcinoma of esophagus.
Adenocarcinoma
[A Case of Unresectable Advanced Rectal Cancer with a Pancreatic Tumor That Was Successfully Treated with FOLFIRINOX].
Adenocarcinoma of Lung
Combination of hesperetin and platinum enhances anticancer effect on lung adenocarcinoma.
Adenocarcinoma of Lung
Identification of lung adenocarcinoma-specific exosome RNAs in peripheral blood by RNA-Seq analysis.
Adenocarcinoma of Lung
Interception of Benzo[a]pyrene-7,8-dione by UDP Glucuronosyltransferases (UGTs) in Human Lung Cells.
Adenocarcinoma of Lung
The UDP-glucuronosyltransferase 2B17 gene deletion polymorphism: sex-specific association with urinary 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol glucuronidation phenotype and risk for lung cancer.
Adenocarcinoma of Lung
UDP-glucuronosyltransferase 2B17 genotype and the risk of lung cancer among Austrian Caucasians.
Adenocarcinoma of Lung
[Correlation of polymorphisms of UDP-glucuronosyltransferase 1A7 gene to genetic susceptibility of lung cancer]
Adenoma
Association of CYP1B1 germ line mutations with hepatocyte nuclear factor 1alpha-mutated hepatocellular adenoma.
Adenoma
C-reactive protein genotypes and haplotypes, polymorphisms in NSAID-metabolizing enzymes, and risk of colorectal polyps.
Adenoma
Chondroitin synthases I, II, III and chondroitin sulfate glucuronyltransferase expression in colorectal cancer.
Adenoma
CYP2C9 and UGT1A6 genotypes modulate the protective effect of aspirin on colon adenoma risk.
Adenoma
Differential down-regulation of the UDP-glucuronosyltransferase 1A locus is an early event in human liver and biliary cancer.
Adenoma
Expression of UDP-glucuronosyltransferase 1A, nuclear factor erythroid-E2-related factor 2 and Kelch-like ECH-associated protein 1 in colonic mucosa, adenoma and adenocarcinoma tissue.
Adenoma
Genetic variants in the UGT1A6 enzyme, aspirin use, and the risk of colorectal adenoma.
Adenoma
Genetic variants of UGT1A6 influence risk of colorectal adenoma recurrence.
Adenoma
No association between cyclooxygenase-2 and uridine diphosphate glucuronosyltransferase 1A6 genetic polymorphisms and colon cancer risk.
Adenoma
Novel Methods of Risk Stratifying Patients for Metachronous, Pre-Malignant Colorectal Polyps: A Systematic Review.
Adenoma
Polymorphisms in heterocyclic aromatic amines metabolism-related genes are associated with colorectal adenoma risk.
Adenoma
Relationship between the Expression of CES2, UGT1A1, and GUSB in colorectal cancer tissues and aberrant methylation.
Adenoma
Relationship between the expression of CES2, UGT1A1, and GUSB in colorectal cancer tissues and aberrant methylation.
Adenoma
The influence of UGT1A6 variants and aspirin use in a randomized trial of celecoxib for prevention of colorectal adenoma.
alpha-Thalassemia
Do Alpha Thalassemia, Fetal Hemoglobin, and the UGT1A1 Polymorphism have an Influence on Serum Bilirubin Levels and Cholelithiasis in Patients with Sickle Cell Disease?
alpha-Thalassemia
Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes.
alpha-Thalassemia
Influence of UGT1A1 promoter polymorphism, ?-thalassemia and ?s haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort.
alpha-Thalassemia
Risk assessment of gene variants for neonatal hyperbilirubinemia in Taiwan.
alpha-Thalassemia
Serum Total Bilirubin, not Cholelithiasis, is Influenced by UGT1A1 Polymorphism, Alpha Thalassemia and ?(s) Haplotype: First Report on Comparison between Arab-Indian and African ?(s) Genes.
alpha-Thalassemia
UGT1A1 (TA)
alpha-Thalassemia
UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemia.
Altitude Sickness
Pharmacokinetics of Acetaminophen and Metformin Hydrochloride in Rats After Exposure to Simulated High Altitude Hypoxia.
Anemia
A case of concomitant Gilbert's syndrome and hereditary spherocytosis.
Anemia
A cross-sectional clinic-based study exploring whether variants within the glutathione S-transferase, haptoglobin and uridine 5'-diphospho-glucuronosyltransferase 1A1 genes are associated with interindividual phenotypic variation in sickle cell anaemia in Jamaica.
Anemia
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
Anemia
Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia.
Anemia
Bilirubin concentrations in thalassemia heterozygotes in university students.
Anemia
Do Alpha Thalassemia, Fetal Hemoglobin, and the UGT1A1 Polymorphism have an Influence on Serum Bilirubin Levels and Cholelithiasis in Patients with Sickle Cell Disease?
Anemia
Early complication in Sickle Cell Anemia children due to A(TA)_n TAA polymorphism at the promoter of UGT1A1 gene.
Anemia
Early complication in sickle cell anemia children due to A(TA)nTAA polymorphism at the promoter of UGT1A1 gene.
Anemia
Genetic diagnosis and pathogenic analysis of an atypical hereditary spherocytosis combined with UGT1A1 partial deficiency: A case report.
Anemia
Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1.
Anemia
Hepatic bilirubin UDP-glucuronyltransferase in patients with sickle cell anemia.
Anemia
Influence of bilirubin uridine diphosphate-glucuronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in children with sickle cell anemia.
Anemia
Influence of SLCO1B1 521T>C, UGT2B7 802C>T and IMPDH1 -106G>A Genetic Polymorphisms on Mycophenolic Acid Levels and Adverse Reactions in Chinese Autoimmune Disease Patients.
Anemia
Influence of UGT1A1 promoter polymorphism, ?-thalassemia and ?s haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort.
Anemia
Serum Total Bilirubin, not Cholelithiasis, is Influenced by UGT1A1 Polymorphism, Alpha Thalassemia and ?(s) Haplotype: First Report on Comparison between Arab-Indian and African ?(s) Genes.
Anemia
The effect of UGT1A1 promoter polymorphism in the development of hyperbilirubinemia and cholelithiasis in hemoglobinopathy patients.
Anemia
The effect of UGT1A1 promoter polymorphism on bilirubin response to hydroxyurea therapy in hemoglobinopathies.
Anemia
UDP-glucuronosyltransferase 1 gene promoter polymorphism is associated with increased serum bilirubin levels and cholecystectomy in patients with sickle cell anemia.
Anemia
UGT1A promoter polymorphisms influence bilirubin response to hydroxyurea therapy in sickle cell anemia.
Anemia
UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemia.
Anemia
UGT1A1 promoter polymorphisms and the development of hyperbilirubinemia and gallbladder disease in children with sickle cell anemia.
Anemia
Uridine diphosphate glucuronosyl transferase 1A (UGT1A1) promoter polymorphism in young patients with sickle cell anaemia: report of the first cohort study from Nigeria.
Anemia, Hemolytic
Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome.
Anemia, Hemolytic
Hereditary spherocytosis in 3 children coexisting with UDP-glucuronyl transferase 1A1 deficiency.
Anemia, Hemolytic
Prevalence of clinically relevant UGT1A alleles and haplotypes in African populations.
Anemia, Hemolytic
Prevalence of UGT1A1 gene polymorphism in patients with hemolytic anemia in southern Brazil.
Anemia, Iron-Deficiency
Bilirubin concentrations in thalassemia heterozygotes in university students.
Anemia, Sickle Cell
(281) Genetic variability of UGT2B7, CYP3A4, CYP3A5 and CYP2B6 DMETs in a sickle cell disease patient cohort.
Anemia, Sickle Cell
A cross-sectional clinic-based study exploring whether variants within the glutathione S-transferase, haptoglobin and uridine 5'-diphospho-glucuronosyltransferase 1A1 genes are associated with interindividual phenotypic variation in sickle cell anaemia in Jamaica.
Anemia, Sickle Cell
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
Anemia, Sickle Cell
Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia.
Anemia, Sickle Cell
Do Alpha Thalassemia, Fetal Hemoglobin, and the UGT1A1 Polymorphism have an Influence on Serum Bilirubin Levels and Cholelithiasis in Patients with Sickle Cell Disease?
Anemia, Sickle Cell
Early complication in Sickle Cell Anemia children due to A(TA)_n TAA polymorphism at the promoter of UGT1A1 gene.
Anemia, Sickle Cell
Early complication in sickle cell anemia children due to A(TA)nTAA polymorphism at the promoter of UGT1A1 gene.
Anemia, Sickle Cell
Early modification of sickle cell disease clinical course by UDP-glucuronosyltransferase 1A1 gene promoter polymorphism.
Anemia, Sickle Cell
Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1.
Anemia, Sickle Cell
Hepatic bilirubin UDP-glucuronyltransferase in patients with sickle cell anemia.
Anemia, Sickle Cell
Influence of bilirubin uridine diphosphate-glucuronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in children with sickle cell anemia.
Anemia, Sickle Cell
Influence of UGT1A1 promoter polymorphism, ?-thalassemia and ?s haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort.
Anemia, Sickle Cell
Serum Total Bilirubin, not Cholelithiasis, is Influenced by UGT1A1 Polymorphism, Alpha Thalassemia and ?(s) Haplotype: First Report on Comparison between Arab-Indian and African ?(s) Genes.
Anemia, Sickle Cell
The effect of UGT1A1 promoter polymorphism on bilirubin response to hydroxyurea therapy in hemoglobinopathies.
Anemia, Sickle Cell
The linear effects of alpha-thalassaemia, the UGT1A1 and HMOX1 polymorphisms on cholelithiasis in sickle cell disease.
Anemia, Sickle Cell
UDP-glucuronosyltransferase 1 gene promoter polymorphism is associated with increased serum bilirubin levels and cholecystectomy in patients with sickle cell anemia.
Anemia, Sickle Cell
UGT1A promoter polymorphisms influence bilirubin response to hydroxyurea therapy in sickle cell anemia.
Anemia, Sickle Cell
UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemia.
Anemia, Sickle Cell
UGT1A1 promoter polymorphism associated with serum bilirubin level in Saudi patients with sickle cell disease.
Anemia, Sickle Cell
UGT1A1 promoter polymorphisms and the development of hyperbilirubinemia and gallbladder disease in children with sickle cell anemia.
Anemia, Sickle Cell
UGT1A1 variation and gallstone formation in sickle cell disease.
Anemia, Sickle Cell
UGT2B7 promoter variant -840G>A contributes to the variability in hepatic clearance of morphine in patients with sickle cell disease.
Anemia, Sickle Cell
Uridine diphosphate glucuronosyl transferase 1A (UGT1A1) promoter polymorphism in young patients with sickle cell anaemia: report of the first cohort study from Nigeria.
Arthritis
Profiling of hepatic metabolizing enzymes and nuclear receptors in rats with adjuvant arthritis by targeted proteomics.
Arthritis, Rheumatoid
Tocilizumab-induced hyperbilirubinemia in Japanese patients with rheumatoid arthritis: its association with UDP glucuronosyltransferase 1A1 gene polymorphisms.
Ascorbic Acid Deficiency
Ascorbic acid deficiency and hepatic UDP-glucuronyl transferase. Qualitative and quantitative differences.
Ascorbic Acid Deficiency
Ascorbic acid deficiency and hepatic UDP-glucuronyltransferase.
Asthma
Genetic variation of genes for xenobiotic-metabolizing enzymes and risk of bronchial asthma: the importance of gene-gene and gene-environment interactions for disease susceptibility.
Asthma, Aspirin-Induced
Characterization of six base pair deletion in the putative HNF1-binding site of human PXR promoter.
Autoimmune Diseases
Influence of SLCO1B1 521T>C, UGT2B7 802C>T and IMPDH1 -106G>A Genetic Polymorphisms on Mycophenolic Acid Levels and Adverse Reactions in Chinese Autoimmune Disease Patients.
beta-Thalassemia
Genetic modulators of sickle cell disease in French Guiana: Markers of the slave trade.
beta-Thalassemia
Gilbert syndrome associated with beta-thalassemia.
beta-Thalassemia
Persistent jaundice in an infant with homozygous beta thalassemia due to co-inherited Crigler-Najjar syndrome.
beta-Thalassemia
Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients.
Biliary Tract Neoplasms
A UGT1A1 genotype-guided dosing study of modified FOLFIRINOX in previously untreated patients with advanced gastrointestinal malignancies.
Biliary Tract Neoplasms
Relationship between UGT1A1*6/*28 polymorphisms and severe toxicities in Chinese patients with pancreatic or biliary tract cancer treated with irinotecan-containing regimens.
Bone Diseases, Metabolic
The importance of the UGT1A1 variants in the development of osteopenia and osteoporosis in postmenopausal women.
Brain Injuries, Traumatic
Effect of Traumatic Brain Injury, Erythropoietin, and Anakinra on Hepatic Metabolizing Enzymes and Transporters in an Experimental Rat Model.
Brain Neoplasms
A phase I/II pharmacokinetics/pharmacodynamics study of irinotecan combined with S-1 for recurrent/metastatic breast cancer in patients with selected UGT1A1 genotypes (the JBCRG-M01 study).
Breast Neoplasms
A phase I/II pharmacokinetics/pharmacodynamics study of irinotecan combined with S-1 for recurrent/metastatic breast cancer in patients with selected UGT1A1 genotypes (the JBCRG-M01 study).
Breast Neoplasms
A signature of balancing selection in the region upstream to the human UGT2B4 gene and implications for breast cancer risk.
Breast Neoplasms
A Uridine Glucuronosyltransferase 2B7 Polymorphism Predicts Epirubicin Clearance and Outcomes in Early-Stage Breast Cancer.
Breast Neoplasms
ABCC2 c.-24 C>T single-nucleotide polymorphism was associated with the pharmacokinetic variability of deferasirox in Chinese subjects.
Breast Neoplasms
Activity Levels of Tamoxifen Metabolites at the Estrogen Receptor and the Impact of Genetic Polymorphisms of Phase I and II Enzymes on Their Concentration Levels in Plasma.
Breast Neoplasms
Age-related changes in mRNA levels of hepatic transporters, cytochrome P450 and UDP-glucuronosyltransferase in female rats.
Breast Neoplasms
Alterations in Hepatic mRNA Expression of Phase-II Enzymes and Xenobiotic Transporters after Targeted Disruption of Hepatocyte Nuclear Factor 4 alpha.
Breast Neoplasms
Androgen and estrogen receptors in breast cancer co-regulate human UDP-glucuronosyltransferases 2B15 and 2B17.
Breast Neoplasms
Antiretroviral therapy-induced liver alterations.
Breast Neoplasms
Association between ESR1, ESR2, HER2, UGT1A4, and UGT2B7 polymorphisms and breast Cancer in Jordan: a case-control study.
Breast Neoplasms
Association between UDP-glucuronosyltransferase 2B7 tagSNPs and breast cancer risk in Chinese females.
Breast Neoplasms
Association of genetic polymorphisms in UGT1A1 with breast cancer and plasma hormone levels.
Breast Neoplasms
Association of genetic variation in tamoxifen-metabolizing enzymes with overall survival and recurrence of disease in breast cancer patients.
Breast Neoplasms
Bilirubin UDP-glucuronosyltransferase 1A1 gene polymorphisms: susceptibility to oxidative damage and cancer?
Breast Neoplasms
Breast Cancer Resistance Protein-Mediated Efflux of Luteolin Glucuronides in HeLa Cells Overexpressing UDP-Glucuronosyltransferase 1A9.
Breast Neoplasms
Characterization of UDP-glucuronosyltransferase (UGT1A1) Promoter Polymorphisms and Gene Expression on Ethnicity, Stage of Disease, and Menopausal Status in Breast Cancer.
Breast Neoplasms
Combined UGT1A1 and UGT1A6 genotypes together with a stressful life event increase breast cancer risk.
Breast Neoplasms
Correction: Impacts of the Glucuronidase Genotypes UGT1A4, UGT2B7, UGT2B15 and UGT2B17 on Tamoxifen Metabolism in Breast Cancer Patients.
Breast Neoplasms
Correlation of UGT2B7 Polymorphism with Cardiotoxicity in Breast Cancer Patients Undergoing Epirubicin/Cyclophosphamide-Docetaxel Adjuvant Chemotherapy.
Breast Neoplasms
CYP2D6 and UGT2B7 Genotype and Risk of Recurrence in Tamoxifen-Treated Breast Cancer Patients.
Breast Neoplasms
Differential effect of over-expressing UGT1A1 and CYP1A1 on xenobiotic assault in MCF-7 cells.
Breast Neoplasms
Disposition of Mianserin and Cyclizine in UGT2B10-Overexpressing Human Embryonic Kidney 293 Cells: Identification of UGT2B10 as a Novel N-Glucosidation Enzyme and Breast Cancer Resistance Protein as an N-Glucoside Transporter.
Breast Neoplasms
Disturbance of Mammary UDP-Glucuronosyltransferase Represses Estrogen Metabolism and Exacerbates Experimental Breast Cancer.
Breast Neoplasms
Effect of Genetic Polymorphisms on the Pharmacokinetics of Deferasirox in Healthy Chinese Subjects and an Artificial Neural Networks Model for Pharmacokinetic Prediction.
Breast Neoplasms
Effects of CYP2D6 and UGT2B7 polymorphisms on pharmacokinetics of tamoxifen in Thai breast cancer patients.
Breast Neoplasms
Efflux excretion of bisdemethoxycurcumin-O-glucuronide in UGT1A1-overexpressing HeLa cells: Identification of breast cancer resistance protein (BCRP) and multidrug resistance-associated proteins 1 (MRP1) as the glucuronide transporters.
Breast Neoplasms
Estrogen pathway polymorphisms and mammographic density.
Breast Neoplasms
Estrogen receptor alpha, fos-related antigen-2, and c-Jun coordinately regulate human UDP glucuronosyltransferase 2B15 and 2B17 expression in response to 17beta-estradiol in MCF-7 cells.
Breast Neoplasms
Estrogen regulation of the glucuronidation enzyme UGT2B15 in estrogen receptor-positive breast cancer cells.
Breast Neoplasms
Evaluation of Tissue Stem Cell-Derived Human Intestinal Organoids, a Physiologically Relevant Model to Evaluate Cytochrome P450 Induction in Gut.
Breast Neoplasms
Evaluation of UDP-glucuronosyltransferase 2B17 (UGT2B17) and dihydrofolate reductase (DHFR) genes deletion and the expression level of NGX6 mRNA in breast cancer.
Breast Neoplasms
Exemestane and Its Active Metabolite 17-Hydroexemestane Induce UDP-Glucuronosyltransferase (UGT) 2B17 Expression in Breast Cancer Cells.
Breast Neoplasms
Exemestane may be less detrimental than letrozole to bone health in women homozygous for the UGT2B17*2 gene deletion.
Breast Neoplasms
Expression and Inducibility of UDP-glucuronosyltransferase 1As in MCF-7 Human Breast Carcinoma Cells.
Breast Neoplasms
Genetic polymorphisms in human SULT1A1 and UGT1A1 genes associate with breast tumor characteristics: a case-series study.
Breast Neoplasms
Genetic Polymorphisms in the UGT1A1 Gene and Breast Cancer Risk in Greek Women.
Breast Neoplasms
Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 (UGT1A1) and risk of breast cancer.
Breast Neoplasms
Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and association with breast cancer among African Americans.
Breast Neoplasms
Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and breast cancer risk in Africans.
Breast Neoplasms
Genetic polymorphisms of drug-metabolising enzymes and drug transporters in the chemotherapeutic treatment of cancer.
Breast Neoplasms
Genetic variants in hormone-related genes and risk of breast cancer.
Breast Neoplasms
Genetic variants of CYP3A5, CYP2D6, SULT1A1, UGT2B15 and tamoxifen response in postmenopausal patients with breast cancer.
Breast Neoplasms
Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia.
Breast Neoplasms
Glucuronidation of the soyabean isoflavones genistein and daidzein by human liver is related to levels of UGT1A1 and UGT1A9 activity and alters isoflavone response in the MCF-7 human breast cancer cell line.
Breast Neoplasms
Gly71Arg UGT1A1 polymorphism is associated with breast cancer susceptibility in Han Chinese women.
Breast Neoplasms
Identification of UDP-glucuronosyltransferase 1A10 in non-malignant and malignant human breast tissues.
Breast Neoplasms
Impact of quercetin?induced changes in drug?metabolizing enzyme and transporter expression on the pharmacokinetics of cyclosporine in rats.
Breast Neoplasms
Impact of UGT2B7 His268Tyr polymorphism on the outcome of adjuvant epirubicin treatment in breast cancer.
Breast Neoplasms
Impacts of the Glucuronidase Genotypes UGT1A4, UGT2B7, UGT2B15 and UGT2B17 on Tamoxifen Metabolism in Breast Cancer Patients.
Breast Neoplasms
Induction of UDP-glucuronosyltransferase 2B15 gene expression by the major active metabolites of tamoxifen, 4-hydroxytamoxifen and endoxifen, in breast cancer cells.
Breast Neoplasms
Investigation of prognostic value of polymorphisms within estrogen metabolizing genes in Lithuanian breast cancer patients.
Breast Neoplasms
Irinotecan pathway genotype analysis to predict pharmacokinetics.
Breast Neoplasms
Mechanism of the efflux transport of demethoxycurcumin-O-glucuronides in HeLa cells stably transfected with UDP-glucuronosyltransferase 1A1.
Breast Neoplasms
Mechanisms and Predictions of Drug-Drug Interactions of the Hepatitis C Virus Three Direct-Acting Antiviral Regimen: Paritaprevir/Ritonavir, Ombitasvir, and Dasabuvir.
Breast Neoplasms
Networking of differentially expressed genes in human cancer cells resistant to methotrexate.
Breast Neoplasms
Novel identification of UDP-glucuronosyltransferase 1A10 as an estrogen-regulated target gene.
Breast Neoplasms
Pazopanib: the newest tyrosine kinase inhibitor for the treatment of advanced or metastatic renal cell carcinoma.
Breast Neoplasms
Pharmacogenetic Analysis of OATP1B1, UGT1A1, and BCRP Variants in Relation to the Pharmacokinetics of Letermovir in Previously Conducted Clinical Studies.
Breast Neoplasms
Pharmacogenetic study of deferasirox, an iron chelating agent.
Breast Neoplasms
Pharmacogenetics in pancreatic cancer. Highlights from the 45th ASCO annual meeting. Orlando, FL, USA. May 29-June 2, 2009.
Breast Neoplasms
Pharmacogenetics of UGT1A4, UGT2B7 and UGT2B15 and Their Influence on Tamoxifen Disposition in Asian Breast Cancer Patients.
Breast Neoplasms
Phase II clinical trial of metronomic chemotherapy with combined irinotecan and tegafur-gimeracil-oteracil potassium in metastatic and recurrent breast cancer.
Breast Neoplasms
Polymorphic variants in NR1I3 and UGT2B7 predict taxane neurotoxicity and have prognostic relevance in breast cancer patients: a case-control study.
Breast Neoplasms
Polymorphisms of ESR1, UGT1A1, HCN1, MAP3K1 and CYP2B6 are associated with the prognosis of hormone receptor-positive early breast cancer.
Breast Neoplasms
Potential influence of UGT1A8 genotype on osteoporosis and breast cancer treatment outcome.
Breast Neoplasms
Prevalence of the UGT1A1*28 promoter polymorphism and breast cancer risk among African American women in Memphis, TN.
Breast Neoplasms
Prognostic impact of genetic variants of CYP19A1 and UGT2B17 in a randomized trial for endocrine-responsive postmenopausal breast cancer.
Breast Neoplasms
Racial differences in genetic factors associated with breast cancer.
Breast Neoplasms
Re: CYP2D6 Genotype and Tamoxifen Response in Postmenopausal Women With Endocrine-Responsive Breast Cancer: The Breast International Group 1-98 Trial and Re: CYP2D6 and UGT2B7 Genotype and Risk of Recurrence in Tamoxifen-Treated Breast Cancer Patients.
Breast Neoplasms
Regioselective Glucuronidation of Diosmetin and Chrysoeriol by the Interplay of Glucuronidation and Transport in UGT1A9-Overexpressing HeLa Cells.
Breast Neoplasms
Representation of CYP3A4, CYP3A5 and UGT1A4 Polymorphisms within Croatian Breast Cancer Patients' Population.
Breast Neoplasms
Resveratrol represses estrogen-induced mammary carcinogenesis through NRF2-UGT1A8-estrogen metabolic axis activation.
Breast Neoplasms
RS7435335 located in the UGT2B7 gene may be a possible genetic marker for the clinical response and prognosis of breast cancer patients receiving neoadjuvant chemotherapy.
Breast Neoplasms
Src supports UDP-glucuronosyltransferase-2B7 detoxification of catechol estrogens associated with breast cancer.
Breast Neoplasms
The association between TA-repeat polymorphism in the promoter region of UGT1A1 and breast cancer risk: a meta-analysis.
Breast Neoplasms
The Effect of Polymorphism in UGT1A4 on Clinical Outcomes of Adjuvant Tamoxifen Therapy for Patients With Breast Cancer in China.
Breast Neoplasms
The influence of genetic polymorphisms on the efficacy and side effects of anastrozole in postmenopausal breast cancer patients.
Breast Neoplasms
UDP-glucuronosyltransferase (UGT) 1A9-overexpressing HeLa cells is an appropriate tool to delineate the kinetic interplay between breast cancer resistance protein (BRCP) and UGT and to rapidly identify the glucuronide substrates of BCRP.
Breast Neoplasms
UDP-glucuronosyltransferase 1A6 overexpression in breast cancer cells resistant to methotrexate.
Breast Neoplasms
UDP-glucuronosyltransferase and sulfotransferase polymorphisms, sex hormone concentrations, and tumor receptor status in breast cancer patients.
Breast Neoplasms
UGT2B4 previously implicated in the risk of breast cancer is associated with menarche timing in Ukrainian females.
Breast Neoplasms
Uridine Glucuronosyltransferase 2B7 Polymorphism-Based Pharmacogenetic Dosing of Epirubicin in FEC Chemotherapy for Early-Stage Breast Cancer.
Breast Neoplasms
[Association of polymorphisms in SULT1A1 and UGT1A1 Genes with breast cancer risk and phenotypes in Russian women]
Breast Neoplasms
[Effect of single nucleotide polymorphisms of RS1826690 located in UGT2B4 gene on the pathological complete response to neoadjuvant chemotherapy in breast cancer patients].
Breast Neoplasms
[Glucuronic acid, glucuronyltransferase and estrogens in breast cancer and precancer]
Breast Neoplasms
[Predictive biomarkers for response to irinotecan, platinum drugs, and taxanes].
Carcinogenesis
Association of genetic polymorphisms in UGT1A1 with breast cancer and plasma hormone levels.
Carcinogenesis
Bile acid inhibition of xenobiotic-metabolizing enzymes is a factor in the mechanism of colon carcinogenesis: tests of aspects of the concept with glucuronosyltransferase.
Carcinogenesis
Characterization of UDP-glucuronosyltransferase (UGT1A1) Promoter Polymorphisms and Gene Expression on Ethnicity, Stage of Disease, and Menopausal Status in Breast Cancer.
Carcinogenesis
Characterization of UDP-glucuronosyltransferase 2A1 (UGT2A1) variants and their potential role in tobacco carcinogenesis.
Carcinogenesis
Combined effect of genetic polymorphisms in phase I and II biotransformation enzymes on head and neck cancer risk.
Carcinogenesis
Cruciferae interact with the UGT1A1*28 polymorphism to determine serum bilirubin levels in humans.
Carcinogenesis
Effect of cigarette smoke on mutagenic activation of environmental carcinogens by cytochrome P450 2A8 and inactivation by glucuronidation in hamster liver.
Carcinogenesis
Effect of ethanol treatment on metabolic activation and detoxification of esophagus carcinogenic N-nitrosamines in rat liver.
Carcinogenesis
Effects of alpha-naphthyl isothiocyanate and a heterocyclic amine, PhIP, on cytochrome P-450, mutagenic activation of various carcinogens and glucuronidation in rat liver.
Carcinogenesis
Effects of anticarcinogenic monoterpenes on phase II hepatic metabolizing enzymes.
Carcinogenesis
Effects of usnic acid exposure on human hepatoblastoma HepG2 cells in culture.
Carcinogenesis
Expression of UDP-glucuronosyltransferase 1A in bladder cancer: Association with prognosis and regulation by estrogen.
Carcinogenesis
Expression of UDP-glucuronosyltransferase 1A, nuclear factor erythroid-E2-related factor 2 and Kelch-like ECH-associated protein 1 in colonic mucosa, adenoma and adenocarcinoma tissue.
Carcinogenesis
Genetic polymorphism in the conjugating enzyme UGT1A1 and the risk of head and neck cancer.
Carcinogenesis
Genetic polymorphisms in CYP1A1, CYP2D6, UGT1A6, UGT1A7, and SULT1A1 genes and correlation with benzene exposure in a Chinese occupational population.
Carcinogenesis
Genetic polymorphisms in the tobacco smoke carcinogens detoxifying enzyme UGT1A7 and the risk of head and neck cancer.
Carcinogenesis
Genetic polymorphisms of the uridine diphosphate glucuronosyltransferase 1A7 and colorectal cancer risk in relation to cigarette smoking and alcohol drinking in a Chinese population.
Carcinogenesis
Genetic variants of UGT1A6 influence risk of colorectal adenoma recurrence.
Carcinogenesis
Identification and functional characterization of a novel UGT2A1 splice variant: Potential importance in tobacco-related cancer susceptibility.
Carcinogenesis
Increased UDP-glucuronyltransferase and gamma-glutamyltranspeptidase in enzyme-altered rat liver lesions produced by low doses of aflatoxin B1.
Carcinogenesis
Modification by curcumin of mutagenic activation of carcinogenic N-nitrosamines by extrahepatic cytochromes P-450 2B1 and 2E1 in rats.
Carcinogenesis
Nrf2-Keap1 signaling pathway regulates human UGT1A1 expression in vitro and in transgenic UGT1 mice.
Carcinogenesis
Polymorphism of UDP-glucuronosyltransferase and drug metabolism.
Carcinogenesis
Polymorphisms of the human UDP-glucuronosyltransferase (UGT) 1A7 gene in colorectal cancer.
Carcinogenesis
Regulation and function of family 1 and family 2 UDP-glucuronosyltransferase genes (UGT1A, UGT2B) in human oesophagus.
Carcinogenesis
Species differences in phenobarbital-mediated UGT gene induction in rat and human liver microtissues.
Carcinogenesis
Sulforaphane suppresses carcinogenesis of colorectal cancer through the ERK/Nrf2?UDP glucuronosyltransferase 1A metabolic axis activation.
Carcinogenesis
Suppression of AhR signaling pathway is associated with the down-regulation of UDP-glucuronosyltransferases during BBN-induced urinary bladder carcinogenesis in mice.
Carcinogenesis
The functional UGT1A1 promoter polymorphism decreases endometrial cancer risk.
Carcinogenesis
The Influence of Curcumin, Quercetin, and Eicosapentaenoic Acid on the Expression of Phase II Detoxification Enzymes in the Intestinal Cell Lines HT-29, Caco-2, HuTu 80, and LT97.
Carcinogenesis
UDP-glucuronosyltransferase 2B17 genotype and the risk of lung cancer among Austrian Caucasians.
Carcinogenesis
UDP-glucuronosyltransferase polymorphisms affect diethylnitrosamine-induced carcinogenesis in humanized transgenic mice.
Carcinogenesis
UDP-glucuronosyltransferase UGT1A7 genetic polymorphisms in hepatocellular carcinoma: a differential impact according to seropositivity of HBV or HCV markers?
Carcinogenesis
[Association between genetic polymorphism of UGT1A7 and susceptibility of bladder cancer]
Carcinogenesis
[The UGT1A, Nrf2 and Keap1 protein expression and significance in colon tumor].
Carcinoid Tumor
Dual polymorphisms in UDP-glucuronosyltransferases 1A1 and 1A6: a novel mechanism for hyperserotoninaemia in Gilbert's syndrome mimicking carcinoid syndrome?
Carcinoma
AH receptor-controlled transcriptional regulation and function of rat and human UDP-glucuronosyltransferase isoforms.
Carcinoma
Alternative-splicing forms of the major phase II conjugating UGT1A gene negatively regulate glucuronidation in human carcinoma cell lines.
Carcinoma
Aryl hydrocarbon receptor-inducible or constitutive expression of human UDP glucuronosyltransferase UGT1A6.
Carcinoma
Association between UGT1A1 Polymorphism and Risk of Laryngeal Squamous Cell Carcinoma.
Carcinoma
Association between UGT1A1*28*28 genotype and lung cancer in the Japanese population.
Carcinoma
Contribution of UGT1A1 genetic polymorphisms related to axitinib pharmacokinetics to safety and efficacy in patients with renal cell carcinoma.
Carcinoma
Detection of UGT1A10 polymorphisms and their association with orolaryngeal carcinoma risk.
Carcinoma
Expression of UDP-glucuronosyltransferase 1A6 isoform in Caco-2 cells stimulated with lipopolysaccharide.
Carcinoma
Expression of UGT2B7, a UDP-glucuronosyltransferase implicated in the metabolism of 4-hydroxyestrone and all-trans retinoic acid, in normal human breast parenchyma and in invasive and in situ breast cancers.
Carcinoma
Genetic polymorphisms in human UDP-glucuronosyltransferases 1A7 and the risk of gastrointestinal carcinomas: A systematic review and network meta-analysis.
Carcinoma
Genetic polymorphisms in the tobacco smoke carcinogens detoxifying enzyme UGT1A7 and the risk of head and neck cancer.
Carcinoma
Germline copy number loss of UGT2B28 and gain of PLEC contribute to increased human esophageal squamous cell carcinoma risk in Southwest China.
Carcinoma
High enzyme activity UGT1A1 or low activity UGT1A8 and UGT2B4 genotypes increase esophageal cancer risk.
Carcinoma
Homozygous deletions of UGT2B17 modifies effects of smoking on TP53-mutations and relapse of head and neck carcinoma.
Carcinoma
Induction of human UDP glucuronosyltransferases (UGT1A6, UGT1A9, and UGT2B7) by t-butylhydroquinone and 2,3,7,8-tetrachlorodibenzo-p-dioxin in Caco-2 cells.
Carcinoma
Pazopanib-Induced Liver Toxicity in Patients With Metastatic Renal Cell Carcinoma: Effect of UGT1A1 Polymorphism on Pazopanib Dose Reduction, Safety, and Patient Outcomes.
Carcinoma
Regulation and function of family 1 and family 2 UDP-glucuronosyltransferase genes (UGT1A, UGT2B) in human oesophagus.
Carcinoma
The association between UGT1A7 polymorphism and cancer risk: A meta-analysis.
Carcinoma
The role of xenobiotic glucuronidating enzymes in drug resistance of tumour tissues and cells.
Carcinoma
UDP-glucuronosyltransferases (UGTs): from purification of Ah-receptor-inducible UGT1A6 to coordinate regulation of subsets of CYPs, UGTs, and ABC transporters by nuclear receptors.
Carcinoma
UGT1A1 polymorphism as a prognostic indicator of stage I ovarian clear cell carcinoma patients treated with irinotecan.
Carcinoma
UGT2B17 and miR-224 contribute to hormone dependency trends in adenocarcinoma and squamous cell carcinoma of esophagus.
Carcinoma
Valproic acid induces neuroendocrine differentiation and UGT2B7 up-regulation in human prostate carcinoma cell line.
Carcinoma
[A Case of Unresectable Advanced Rectal Cancer with a Pancreatic Tumor That Was Successfully Treated with FOLFIRINOX].
Carcinoma
[Correlation of polymorphisms of UDP-glucuronosyltransferase 1A7 gene to genetic susceptibility of lung cancer]
Carcinoma
[The UGT1A, Nrf2 and Keap1 protein expression and significance in colon tumor].
Carcinoma, Hepatocellular
Ages of hepatocellular carcinoma occurrence and life expectancy are associated with a UGT2B28 genomic variation.
Carcinoma, Hepatocellular
Bisphenol A induces Nrf2-dependent drug-metabolizing enzymes through nitrosylation of Keap1.
Carcinoma, Hepatocellular
C/EBPalpha is a regulator of the UDP glucuronosyltransferase UGT2B1 gene.
Carcinoma, Hepatocellular
Cloning and characterization of cDNAs encoding mouse Ugt1.6 and rabbit UGT1.6: differential induction by 2,3,7,8-tetrachlorodibenzo-p-dioxin.
Carcinoma, Hepatocellular
Contribution of the Ah receptor to the phenolic antioxidant-mediated expression of human and rat UDP-glucuronosyltransferase UGT1A6 in Caco-2 and rat hepatoma 5L cells.
Carcinoma, Hepatocellular
Development and application of test methods for the detection of dietary constituents which protect against heterocyclic aromatic amines.
Carcinoma, Hepatocellular
Different properties of microsomal UDP-glucuronyltransferase in buffalo rat liver and a clonal strain of rat hepatoma cells derived from the same rat strain.
Carcinoma, Hepatocellular
Differential down-regulation of the UDP-glucuronosyltransferase 1A locus is an early event in human liver and biliary cancer.
Carcinoma, Hepatocellular
Effect of aflatoxin B1 on UDP-glucuronosyltransferase mRNA expression in HepG2 cells.
Carcinoma, Hepatocellular
Epigenetic regulation of UDP-Glucuronosyltransferase by microRNA-200a/-183: implications for responses to sorafenib treatment in patients with hepatocellular carcinoma.
Carcinoma, Hepatocellular
Epirubicin Upregulates UDP Glucuronosyltransferase 2B7 Expression in Liver Cancer Cells Via the p53 Pathway.
Carcinoma, Hepatocellular
Genetic link of hepatocellular carcinoma with polymorphisms of the UDP-glucuronosyltransferase UGT1A7 gene.
Carcinoma, Hepatocellular
Genetic polymorphisms in human UDP-glucuronosyltransferases 1A7 and the risk of gastrointestinal carcinomas: A systematic review and network meta-analysis.
Carcinoma, Hepatocellular
Glucuronyltransferase activity in transplantable rat hepatomas.
Carcinoma, Hepatocellular
Glycoside conjugation in microsomes from hepatic and renal carcinoma of man.
Carcinoma, Hepatocellular
Identification and characterization of genes associated with human hepatocellular carcinogenesis.
Carcinoma, Hepatocellular
Increased expression of drug-metabolizing enzymes in human hepatocarcinoma FLC-4 cells cultured on micro-space cell culture plates.
Carcinoma, Hepatocellular
Inducibility of UDP-glucuronosyltransferase 1As by beta-naphthoflavone in HepG2 cells.
Carcinoma, Hepatocellular
Induction of Human UDP-glucuronosyltransferase 2B7 Gene Expression by Cytotoxic Anticancer Drugs in Liver Cancer HepG2 Cells.
Carcinoma, Hepatocellular
Induction of UDP-glucuronosyltransferase 1A8 mRNA by 3-methylcholanthene in rat hepatoma cells.
Carcinoma, Hepatocellular
Induction of UDP-glucuronosyltransferase activity in the Reuber H-4-II-E hepatoma cell culture.
Carcinoma, Hepatocellular
Induction of UDP-glucuronosyltransferase UGT1A1 by the flavonoid chrysin in the human hepatoma cell line hep G2.
Carcinoma, Hepatocellular
Involvement of the xenobiotic response element (XRE) in Ah receptor-mediated induction of human UDP-glucuronosyltransferase 1A1.
Carcinoma, Hepatocellular
Mixed function oxidase and UDP-glucuronyltransferase activities in the human Hep G2 hepatoma cell line.
Carcinoma, Hepatocellular
Nuclear factor ?B down-regulates human UDP-glucuronosyltransferase 1A1: a novel mechanism involved in inflammation-associated hyperbilirubinaemia.
Carcinoma, Hepatocellular
Occurrence of steroid glucuronyltransferases in a hepatoma.
Carcinoma, Hepatocellular
Persistently increased expression of a 3-methylcholanthrene-inducible phenol uridine diphosphate-glucuronosyltransferase in rat hepatocyte nodules and hepatocellular carcinomas.
Carcinoma, Hepatocellular
Pharmacokinetic interaction involving sorafenib and the calcium-channel blocker felodipine in a patient with hepatocellular carcinoma.
Carcinoma, Hepatocellular
Proceedings: Substrate specificity of UDP-glucuronyltransferase in rat liver and in Morris hepatomas: studies on a connection with the monooxygenase-epoxide hydrase system.
Carcinoma, Hepatocellular
Quantitative relationship of UDP- glucuronosyltransferase to the NADPH and NADH electron-transport systems in Morris hepatomas with varying growth rates.
Carcinoma, Hepatocellular
Regulation of UDP-Glucuronosyltransferases UGT2B4 and UGT2B7 by MicroRNAs in Liver Cancer Cells.
Carcinoma, Hepatocellular
The effects of inducing agents on cytochrome P450 and UDP-glucuronyltransferase activities in human HEPG2 hepatoma cells.
Carcinoma, Hepatocellular
The role of chrysin and the ah receptor in induction of the human UGT1A1 gene in vitro and in transgenic UGT1 mice.
Carcinoma, Hepatocellular
Transcriptional Regulation of Human UDP-Glucuronosyltransferase 2B10 by Farnesoid X Receptor in Human Hepatoma HepG2 Cells.
Carcinoma, Hepatocellular
UDP-glucuronosyltransferase 1A7 genetic polymorphisms are associated with hepatocellular carcinoma in japanese patients with hepatitis C virus infection.
Carcinoma, Hepatocellular
UDP-glucuronosyltransferase 1A7 genetic polymorphisms are associated with hepatocellular carcinoma risk and onset age.
Carcinoma, Hepatocellular
UDP-glucuronosyltransferase 1A7 polymorphisms are associated with liver cirrhosis.
Carcinoma, Hepatocellular
UDP-glucuronosyltransferase polymorphisms affect diethylnitrosamine-induced carcinogenesis in humanized transgenic mice.
Carcinoma, Hepatocellular
UDP-glucuronosyltransferase UGT1A7 genetic polymorphisms in hepatocellular carcinoma: a differential impact according to seropositivity of HBV or HCV markers?
Carcinoma, Hepatocellular
UGT1A polymorphisms as genetic biomarkers for hepatocellular carcinoma risk in Caucasian population.
Carcinoma, Hepatocellular
UGT1A7 haplotype is associated with an increased risk of hepatocellular carcinoma in hepatitis B carriers.
Carcinoma, Hepatocellular
Variation of hepatic glucuronidation: Novel functional polymorphisms of the UDP-glucuronosyltransferase UGT1A4.
Carcinoma, Hepatocellular
[Genetic polymorphism of UDP-glucuronosyltransferase 1F and susceptibility to hepatocellular carcinoma]
Carcinoma, Non-Small-Cell Lung
Correlations of UGT1A1 gene polymorphisms with onset and prognosis of non-small cell lung cancer.
Carcinoma, Non-Small-Cell Lung
Phase I/II pharmacokinetic and pharmacogenomic study of UGT1A1 polymorphism in elderly patients with advanced non-small cell lung cancer treated with irinotecan.
Carcinoma, Non-Small-Cell Lung
Potentially functional genetic variants in PLIN2, SULT2A1 and UGT1A9 genes of the ketone pathway and survival of nonsmall cell lung cancer.
Carcinoma, Non-Small-Cell Lung
Weekly regimen of irinotecan/docetaxel in previously treated non-small cell lung cancer patients and correlation with uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) polymorphism.
Carcinoma, Renal Cell
Contribution of UGT1A1 genetic polymorphisms related to axitinib pharmacokinetics to safety and efficacy in patients with renal cell carcinoma.
Carcinoma, Renal Cell
Pazopanib-Induced Liver Toxicity in Patients With Metastatic Renal Cell Carcinoma: Effect of UGT1A1 Polymorphism on Pazopanib Dose Reduction, Safety, and Patient Outcomes.
Carcinoma, Squamous Cell
Association between UGT1A1*28*28 genotype and lung cancer in the Japanese population.
Carcinoma, Squamous Cell
UGT2B17 and miR-224 contribute to hormone dependency trends in adenocarcinoma and squamous cell carcinoma of esophagus.
Carcinoma, Squamous Cell
[Correlation of polymorphisms of UDP-glucuronosyltransferase 1A7 gene to genetic susceptibility of lung cancer]
Cardiomyopathies
Clinical and Genetic Determinants of Cardiomyopathy Risk among Hematopoietic Cell Transplantation Survivors.
Cardiotoxicity
Correlation of UGT2B7 Polymorphism with Cardiotoxicity in Breast Cancer Patients Undergoing Epirubicin/Cyclophosphamide-Docetaxel Adjuvant Chemotherapy.
Cardiotoxicity
Pharmacogenetic testing to guide therapeutic decision-making and improve outcomes for children undergoing anthracycline-based chemotherapy.
Cardiotoxicity
Validation of Variants in SLC28A3 and UGT1A6 as Genetic Markers Predictive of Anthracycline-Induced Cardiotoxicity in Children.
Cardiovascular Diseases
Bilirubin, renal hemodynamics, and blood pressure.
Cardiovascular Diseases
Mixed modeling of meta-analysis P-values (MixMAP) suggests multiple novel gene loci for low density lipoprotein cholesterol.
Cardiovascular Diseases
Relation of Conjugated Bilirubin Concentrations to the Presence of Coronary Artery Calcium.
Cardiovascular Diseases
The Implication of the Polymorphisms of COX-1, UGT1A6, and CYP2C9 among Cardiovascular Disease (CVD) Patients Treated with Aspirin.
Cardiovascular Diseases
Three novel single nucleotide polymorphisms in UGT1A9.
Cerebrovascular Disorders
Association between the UGT1A1 TA-repeat polymorphism and bilirubin concentration in patients with intermittent claudication: results from the CAVASIC study.
Chemical and Drug Induced Liver Injury
Absence of significant association between UGT2B4 genetic variants and the susceptibility to anti-tuberculosis drug-induced liver injury in a Western Chinese population.
Chemical and Drug Induced Liver Injury
Association of CYP2C19 and UGT1A4 polymorphisms with voriconazole-induced liver injury.
Chemical and Drug Induced Liver Injury
Comparison of the inhibition potentials of icotinib and erlotinib against human UDP-glucuronosyltransferase 1A1.
Cholangiocarcinoma
Differential down-regulation of the UDP-glucuronosyltransferase 1A locus is an early event in human liver and biliary cancer.
Cholangitis, Sclerosing
Genetic variants of UDP-glucuronosyltransferase 1A genes are associated with disease presentation and outcome in primary sclerosing cholangitis.
Choledocholithiasis
Uridine diphosphate glucuronosyl transferase 1A1 promoter polymorphism is associated with choledocholithiasis in Taiwanese patients.
Cholelithiasis
Association between promoter and coding region mutations of UDP-glucuronosyltransferase 1A1 and beta-thalassemia/Hb E with cholelithiasis.
Cholelithiasis
Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia.
Cholelithiasis
Cholelithiasis in thalassemia major.
Cholelithiasis
Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next-generation sequencing: First South Asian study.
Cholelithiasis
Do Alpha Thalassemia, Fetal Hemoglobin, and the UGT1A1 Polymorphism have an Influence on Serum Bilirubin Levels and Cholelithiasis in Patients with Sickle Cell Disease?
Cholelithiasis
Early complication in Sickle Cell Anemia children due to A(TA)_n TAA polymorphism at the promoter of UGT1A1 gene.
Cholelithiasis
Early modification of sickle cell disease clinical course by UDP-glucuronosyltransferase 1A1 gene promoter polymorphism.
Cholelithiasis
Effect of Mutations on mRNA and Globin Stability: The Cases of Hb Bernalda/Groene Hart and Hb Southern Italy.
Cholelithiasis
Effects of variant UDP-glucuronosyltransferase 1A1 gene, glucose-6-phosphate dehydrogenase deficiency and thalassemia on cholelithiasis.
Cholelithiasis
Gallstone disease in Swedish twins is associated with the Gilbert variant of UGT1A1.
Cholelithiasis
Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1.
Cholelithiasis
Gilbert syndrome acts as a risk factor of developing gallstone among ? hemoglobinopathy Tunisian patients.
Cholelithiasis
Gilbert Syndrome as a Predisposing Factor for Cholelithiasis Risk in the Greek Adult Population.
Cholelithiasis
Gilbert syndrome as a predisposing factor for cholelithiasis risk in the Greek adult population.
Cholelithiasis
Gilbert's syndrome as a predisposing factor for idiopathic cholelithiasis in children.
Cholelithiasis
Implication of genetic variation at the promoter and exon1 of UGT1A1 in occurrence of cholelithiasis in Tunisia.
Cholelithiasis
Influence of bilirubin uridine diphosphate-glucuronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in children with sickle cell anemia.
Cholelithiasis
Influence of UGT1A1 promoter polymorphism, ?-thalassemia and ?s haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort.
Cholelithiasis
Loci From a Genome-Wide Analysis of Bilirubin Levels Are Associated With Gallstone Risk and Composition.
Cholelithiasis
Serum Total Bilirubin, not Cholelithiasis, is Influenced by UGT1A1 Polymorphism, Alpha Thalassemia and ?(s) Haplotype: First Report on Comparison between Arab-Indian and African ?(s) Genes.
Cholelithiasis
The effect of UGT1A1 promoter polymorphism in the development of hyperbilirubinemia and cholelithiasis in hemoglobinopathy patients.
Cholelithiasis
The linear effects of alpha-thalassaemia, the UGT1A1 and HMOX1 polymorphisms on cholelithiasis in sickle cell disease.
Cholelithiasis
UGT1A1 (TA)
Cholelithiasis
UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemia.
Cholestasis
Altered expression of MRP2, MRP3 and UGT2B1 in the liver affects the disposition of morphine and its glucuronide conjugate in a rat model of cholestasis.
Cholestasis
Dose-related increase in liver heme catabolism during rabbit aflatoxicosis.
Cholestasis
Identification of UDP glycosyltransferase 3A1 as a UDP N-acetylglucosaminyltransferase.
Cholestasis
Regulation of the human bile acid UDP-glucuronosyltransferase 1A3 by the farnesoid X receptor and bile acids.
Cholestasis
The effects of total parenteral nutrition on the hepatic handling of bilirubin in the rat.
Cholestasis
The human UGT1A3 enzyme conjugates norursodeoxycholic acid into a C23-ester glucuronide in the liver.
Cholestasis
Unexplained cholestasis in adults and adolescents: diagnostic benefit of genetic examination.
Cholestasis
Upregulation of UGT2B4 Expression by 3'-Phosphoadenosine-5'-Phosphosulfate Synthase Knockdown: Implications for Coordinated Control of Bile Acid Conjugation.
Cholestasis
Yinchenhao Decoction Ameliorates Alpha-Naphthylisothiocyanate Induced Intrahepatic Cholestasis in Rats by Regulating Phase II Metabolic Enzymes and Transporters.
Cholestasis
[Phospholipid composition of the hepatic microsomal membrane and its relationship to bilirubin UDP glucuronyltransferase in human cholestasis]
Cholestasis, Intrahepatic
Pyrimidine-5'-nucleotidase Campinas, a new mutation (p.R56G) in the NT5C3 gene associated with pyrimidine-5'-nucleotidase type I deficiency and influence of Gilbert's Syndrome on clinical expression.
Choline Deficiency
The effect of choline deficiency on the activity of a phosphatidylcholine-requiring enzyme: activity and properties of UDP-glucuronyltransferase in choline-deficient rats.
Coinfection
Interactions with other human UDP-glucuronosyltransferases attenuate the consequences of the Y485D mutation on the activity and substrate affinity of UGT1A6.
Colitis
Bacterial Outer Membrane Vesicles from Dextran Sulfate Sodium-Induced Colitis Differentially Regulate Intestinal UDP-Glucuronosyltransferase 1A1 Partially Through Toll-Like Receptor 4/Mitogen-Activated Protein Kinase/Phosphatidylinositol 3-Kinase Pathway.
Colitis
Disturbance of Hepatic and Intestinal UDP-Glucuronosyltransferase in Rats with Trinitrobenzene Sulfonic Acid-Induced Colitis.
Colitis
Insight into the pharmacokinetic behavior of tanshinone IIA in the treatment of Crohn's disease: comparative data for tanshinone IIA and its two glucuronidated metabolites in normal and recurrent colitis models after oral administration.
Colitis, Ulcerative
Expression of selected cytochrome P450 isoforms and of cooperating enzymes in colorectal tissues in selected pathological conditions.
Colonic Neoplasms
Bile acid inhibition of xenobiotic-metabolizing enzymes is a factor in the mechanism of colon carcinogenesis: tests of aspects of the concept with glucuronosyltransferase.
Colonic Neoplasms
Concurrence of UGT1A polymorphism and end-stage renal disease leads to severe toxicities of irinotecan in a patient with metastatic colon cancer.
Colonic Neoplasms
Cross-Talk between Alternatively Spliced UGT1A Isoforms and Colon Cancer Cell Metabolism.
Colonic Neoplasms
Dapagliflozin Inhibits Cell Adhesion to Collagen I and IV and Increases Ectodomain Proteolytic Cleavage of DDR1 by Increasing ADAM10 Activity.
Colonic Neoplasms
Differential activation of pregnane X receptor by carnosic acid, carnosol, ursolic acid, and rosmarinic acid.
Colonic Neoplasms
Dual deficiency of DPD and UGT1A1 in a case of colon cancer.
Colonic Neoplasms
Effects of co-treatment with sulforaphane and autophagy modulators on uridine 5'-diphospho-glucuronosyltransferase 1A isoforms and cytochrome P450 3A4 expression in Caco-2 human colon cancer cells.
Colonic Neoplasms
Effects of phytochemicals sulforaphane on uridine diphosphate-glucuronosyltransferase expression as well as cell-cycle arrest and apoptosis in human colon cancer Caco-2 cells.
Colonic Neoplasms
FOLFIRI and regorafenib combination therapy with dose escalation of irinotecan as fourth-line treatment for patients with metastatic colon cancer according to UGT1A1 genotyping.
Colonic Neoplasms
Glucuronidation of PhIP and N-OH-PhIP by UDP-glucuronosyltransferase 1A10.
Colonic Neoplasms
Hydroxylated Chalcones as Aryl Hydrocarbon Receptor Agonists: Structure-Activity Effects.
Colonic Neoplasms
Irinotecan cytotoxicity does not necessarily depend on the UGT1A1 polymorphism but on fluoropyrimidine: a molecular case report.
Colonic Neoplasms
Irinotecan inactivation is modulated by epigenetic silencing of UGT1A1 in colon cancer.
Colonic Neoplasms
Isoflavones as Ah Receptor Agonists in Colon-Derived Cell Lines: Structure-Activity Relationships.
Colonic Neoplasms
Joint effects between UDP-glucuronosyltransferase 1A7 genotype and dietary carcinogen exposure on risk of colon cancer.
Colonic Neoplasms
Modulation of colonic xenobiotic metabolizing enzymes by feeding bile acids: comparative effects of cholic, deoxycholic, lithocholic and ursodeoxycholic acids.
Colonic Neoplasms
Modulation of NRF2 and UGT1A expression by epigallocatechin-3-gallate in colon cancer cells and BALB/c mice.
Colonic Neoplasms
No association between cyclooxygenase-2 and uridine diphosphate glucuronosyltransferase 1A6 genetic polymorphisms and colon cancer risk.
Colonic Neoplasms
Reduction of p53 by knockdown of the UGT1 locus in colon epithelial cells causes an increase in tumorigenesis.
Colonic Neoplasms
Regulation of UGT1A1 and HNF1 transcription factor gene expression by DNA methylation in colon cancer cells.
Colonic Neoplasms
Serotonin glucuronidation by Ah receptor- and oxidative stress-inducible human UDP-glucuronosyltransferase (UGT) 1A6 in Caco-2 cells.
Colonic Neoplasms
Structure-Dependent Modulation of Aryl Hydrocarbon Receptor-Mediated Activities by Flavones.
Colonic Neoplasms
The cost-effectiveness of UGT1A1 genotyping before colorectal cancer treatment with irinotecan from the perspective of the German statutory health insurance.
Colonic Neoplasms
UDP-glucuronosyltransferase 1A compromises intracellular accumulation and anti-cancer effect of tanshinone IIA in human colon cancer cells.
Colonic Neoplasms
UDP-Glucuronosyltransferase 1A Determinates Intracellular Accumulation and Anti-Cancer Effect of ?-Lapachone in Human Colon Cancer Cells.
Colonic Neoplasms
UGT1A1 and UGT1A9 functional variants, meat intake, and colon cancer, among Caucasians and African-Americans.
Colonic Neoplasms
[Effects of autophagy modulator on autophagy and uridine 5'-diphospho-glucuronosyltransferase 1A1 induced by sulforaphane].
Colonic Neoplasms
[The role of NF-E2-related factor 2 in the induction of uridine 5'-diphosphate-glucuronosyltransferase 1A and its isoforms by epigallocatechin gallate in colon cancer cells]
Colorectal Neoplasms
A novel genetic score model of UGT1A1 and TGFB pathway as predictor of severe irinotecan-related diarrhea in metastatic colorectal cancer patients.
Colorectal Neoplasms
A novel system for predicting the toxicity of irinotecan based on statistical pattern recognition with UGT1A genotypes.
Colorectal Neoplasms
A personalized approach to cancer treatment: how biomarkers can help.
Colorectal Neoplasms
A Phase I Study of UGT1A1 * 28/ * 6 Genotype-Directed Dosing of Irinotecan (CPT-11) in Korean Patients with Metastatic Colorectal Cancer Receiving FOLFIRI.
Colorectal Neoplasms
A Phase II study of clinical outcomes of 3-week cycles of irinotecan and S-1 in patients with previously untreated metastatic colorectal cancer: influence of the UGT1A1 and CYP2A6 polymorphisms on clinical activity.
Colorectal Neoplasms
A phase II study of FOLFOXIRI with bevacizumab in untreated metastatic colorectal cancer patients: A UGT1A1 genotype and safety results (QUATTRO study).
Colorectal Neoplasms
A pilot study on the safety of combining chrysin, a non-absorbable inducer of UGT1A1, and irinotecan (CPT-11) to treat metastatic colorectal cancer.
Colorectal Neoplasms
A study of the association between UGT1A1*28 variant allele of UGT1A1 gene and colonic phenotype of sporadic colorectal cancer.
Colorectal Neoplasms
A UGT1A1*28 and *6 genotype-directed phase I dose-escalation trial of irinotecan with fixed-dose capecitabine in Korean patients with metastatic colorectal cancer.
Colorectal Neoplasms
ABCB1, SLCO1B1 and UGT1A1 gene polymorphisms are associated with toxicity in metastatic colorectal cancer patients treated with first-line irinotecan.
Colorectal Neoplasms
An internally and externally validated nomogram for predicting the risk of irinotecan-induced severe neutropenia in advanced colorectal cancer patients.
Colorectal Neoplasms
Association between Polymorphisms in UDP- glucuronosyltransferase 1A6 and 1A7 and Colorectal Cancer Risk.
Colorectal Neoplasms
Association of serum bilirubin and promoter variations in HMOX1 and UGT1A1 genes with sporadic colorectal cancer.
Colorectal Neoplasms
Association of UGT1A1*28 polymorphisms with irinotecan-induced toxicities in colorectal cancer: a meta-analysis in Caucasians.
Colorectal Neoplasms
Associations between UGT2B7 polymorphisms and cancer susceptibility: A meta-analysis.
Colorectal Neoplasms
Brain-derived neurotrophic factor involved epigenetic repression of UGT2B7 in colorectal carcinoma: A mechanism to alter morphine glucuronidation in tumor.
Colorectal Neoplasms
Can UGT1A1 genotyping reduce morbidity and mortality in patients with metastatic colorectal cancer treated with irinotecan? An evidence-based review.
Colorectal Neoplasms
Clinical Implication of UGT1A1 Promoter Polymorphism for Irinotecan Dose Escalation in Metastatic Colorectal Cancer Patients Treated with Bevacizumab Combined with FOLFIRI in the First-line Setting.
Colorectal Neoplasms
Clinical significance of UGT1A1 gene polymorphisms on irinotecan-based regimens as the treatment in metastatic colorectal cancer.
Colorectal Neoplasms
Clinical utility of ABCB1 genotyping for preventing toxicity in treatment with irinotecan.
Colorectal Neoplasms
Correlation between plasma concentration ratios of SN-38 glucuronide and SN-38 and neutropenia induction in patients with colorectal cancer and wild-type UGT1A1 gene.
Colorectal Neoplasms
Correlation between UGT1A1 gene polymorphism and irinotecan chemotherapy in metastatic colorectal cancer: a study from Guangxi Zhuang.
Colorectal Neoplasms
Correlative analysis of plasma SN-38 levels and DPD activity with outcomes of FOLFIRI regimen for metastatic colorectal cancer with UGT1A1 *28 and *6 wild type and its implication for individualized chemotherapy.
Colorectal Neoplasms
Cost effectiveness of pharmacogenetic testing for uridine diphosphate glucuronosyltransferase 1A1 before irinotecan administration for metastatic colorectal cancer.
Colorectal Neoplasms
Cost-Effectiveness Analysis of Ugt1a1 Genotyping Before Colorectal Cancer Treatment with Irinotecan.
Colorectal Neoplasms
Cost-effectiveness of UGT1A1 genotyping in second-line, high-dose, once every 3 weeks irinotecan monotherapy treatment of colorectal cancer.
Colorectal Neoplasms
Cost-effectiveness of UGT1A1*28 genotyping in preventing severe neutropenia following FOLFIRI therapy in colorectal cancer.
Colorectal Neoplasms
CpG island methylation of BNIP3 predicts resistance against S-1/CPT-11 combined therapy in colorectal cancer patients.
Colorectal Neoplasms
Determination of the UGT1A1 polymorphism as guidance for irinotecan dose escalation in metastatic colorectal cancer treated with first-line bevacizumab and FOLFIRI (PURE FIST).
Colorectal Neoplasms
Development of Pyrosequencing Method for Detection of UGT1A1 Polymorphisms in Thai Colorectal Cancers.
Colorectal Neoplasms
Dose adjustment of irinotecan based on UGT1A1 polymorphisms in patients with colorectal cancer.
Colorectal Neoplasms
DPD and UGT1A1 deficiency in colorectal cancer patients receiving triplet chemotherapy with fluoropyrimidines, oxaliplatin and irinotecan.
Colorectal Neoplasms
Effect of drug metabolizing enzymes and transporters in Thai colorectal cancer patients treated with irinotecan-based chemotherapy.
Colorectal Neoplasms
Erratum to: UDP-glucuronosyltransferase 1A1*6 and *28 polymorphisms as indicators of initial dose level of irinotecan to reduce risk of neutropenia in patients receiving FOLFIRI for colorectal cancer.
Colorectal Neoplasms
Examination of multiple UGT1A and DPYD polymorphisms has limited ability to predict the toxicity and efficacy of metastatic colorectal cancer treated with irinotecan-based chemotherapy: a retrospective analysis.
Colorectal Neoplasms
Expression Patterns of Xenobiotic-Metabolizing Enzymes in Tumor and Adjacent Normal Mucosa Tissues among Patients with Colorectal Cancer: The ColoCare Study.
Colorectal Neoplasms
Feasibility of Integrating Panel-Based Pharmacogenomics Testing for Chemotherapy and Supportive Care in Patients With Colorectal Cancer.
Colorectal Neoplasms
Feasibility of preemptive pharmacogenetic testing in colorectal cancer patients within a community oncology setting.
Colorectal Neoplasms
FOLFIRI and regorafenib combination therapy with dose escalation of irinotecan as fourth-line treatment for patients with metastatic colon cancer according to UGT1A1 genotyping.
Colorectal Neoplasms
FOLFIRI Combined with Bevacizumab as First-Line Treatment for Metastatic Colorectal Cancer Patients with Hyperbilirubinemia after UGT1A1 Genotyping.
Colorectal Neoplasms
Genetic polymorphism in UDP-glucuronosyltransferase 2B7 and colorectal cancer risk.
Colorectal Neoplasms
Genetic polymorphisms in human UDP-glucuronosyltransferases 1A7 and the risk of gastrointestinal carcinomas: A systematic review and network meta-analysis.
Colorectal Neoplasms
Genetic polymorphisms of the uridine diphosphate glucuronosyltransferase 1A7 and colorectal cancer risk in relation to cigarette smoking and alcohol drinking in a Chinese population.
Colorectal Neoplasms
Genetic variation in UGT genes modify the associations of NSAIDs with risk of colorectal cancer: Colon cancer family registry.
Colorectal Neoplasms
Gilbert's Syndrome and Irinotecan Toxicity: Combination with UDP-Glucuronosyltransferase 1A7 Variants Increases Risk.
Colorectal Neoplasms
High Resectability Rate of Initially Unresectable Colorectal Liver Metastases After UGT1A1-Adapted High-Dose Irinotecan Combined with LV5FU2 and Cetuximab: A Multicenter Phase II Study (ERBIFORT).
Colorectal Neoplasms
High-Dose FOLFIRI plus Bevacizumab in the Treatment of Metastatic Colorectal Cancer Patients with Two Different UGT1A1 Genotypes: FFCD 0504 Study.
Colorectal Neoplasms
Impact of UGT1A1 genotype on the efficacy and safety of irinotecan-based chemotherapy in metastatic colorectal cancer.
Colorectal Neoplasms
Influence of UGT1A1 gene methylation level in colorectal cancer cells on the sensitivity of the chemotherapy drug CPT-11.
Colorectal Neoplasms
Interactions between CYP2C9 and UGT1A6 polymorphisms and nonsteroidal anti-inflammatory drugs in colorectal cancer prevention.
Colorectal Neoplasms
Link between colorectal cancer and polymorphisms in the uridine-diphosphoglucuronosyltransferase 1A7 and 1A1 genes.
Colorectal Neoplasms
No evidence that polymorphisms in CYP2C8, CYP2C9, UGT1A6, PPARdelta and PPARgamma act as modifiers of the protective effect of regular NSAID use on the risk of colorectal carcinoma.
Colorectal Neoplasms
Novel personalized medicine technology: UGT1A1 testing for irinotecan as a case study.
Colorectal Neoplasms
Oncologic Outcomes in Metastatic Colorectal Cancer with Regorafenib with FOLFIRI as a Third- or Fourth-Line Setting.
Colorectal Neoplasms
Pharmacogenetic clinical randomised phase II trial to evaluate the efficacy and safety of FOLFIRI with high-dose irinotecan (HD-FOLFIRI) in metastatic colorectal cancer patients according to their UGT1A 1 genotype.
Colorectal Neoplasms
Pharmacogenetic clinical randomized phase II trial to evaluate the efficacy and safety of FOLFIRI with high dose of irinotecan (FOLFIRI-HD) in metastatic colorectal cancer patients according to UGT1A 1 genotype.
Colorectal Neoplasms
Pharmacogenetic tailoring of irinotecan-based first-line chemotherapy in metastatic colorectal cancer: results of a pilot study.
Colorectal Neoplasms
Pharmacogenetics of irinotecan: clinical perspectives on the utility of genotyping.
Colorectal Neoplasms
Pharmacogenetics of solid tumors: directed therapy in breast, lung, and colorectal cancer: a paper from the 2008 william beaumont hospital symposium on molecular pathology.
Colorectal Neoplasms
Pharmacokinetic and pharmacogenetic determinants of the activity and toxicity of irinotecan in metastatic colorectal cancer patients.
Colorectal Neoplasms
Pharmacokinetics, safety, and efficacy of FOLFIRI plus bevacizumab in Japanese colorectal cancer patients with UGT1A1 gene polymorphisms.
Colorectal Neoplasms
Phase I/II Study of FOLFIRI in Japanese Patients with Advanced Colorectal Cancer.
Colorectal Neoplasms
Polymorphic Expression of UDP-Glucuronosyltransferase UGTlA Gene in Human Colorectal Cancer.
Colorectal Neoplasms
Polymorphisms of the human UDP-glucuronosyltransferase (UGT) 1A7 gene in colorectal cancer.
Colorectal Neoplasms
Prediction of irinotecan and 5-fluorouracil toxicity and response in patients with advanced colorectal cancer.
Colorectal Neoplasms
Predictive and prognostic biomarkers with therapeutic targets in breast, colorectal, and non-small cell lung cancers: A systemic review of current development, evidence, and recommendation.
Colorectal Neoplasms
Predictive effects of bilirubin on response of colorectal cancer to irinotecan-based chemotherapy.
Colorectal Neoplasms
Predictive Role of the UGT1A1, UGT1A7, and UGT1A9 Genetic Variants and Their Haplotypes on the Outcome of Metastatic Colorectal Cancer Patients Treated With Fluorouracil, Leucovorin, and Irinotecan.
Colorectal Neoplasms
Prognostic advantage of irinotecan dose escalation according to uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) genotyping in patients with metastatic colorectal cancer treated with bevacizumab combined with 5-fluorouracil/leucovorin with irinotecan in a first-line setting.
Colorectal Neoplasms
Promoter length polymorphism in UGT1A1 and the risk of sporadic colorectal cancer.
Colorectal Neoplasms
Prospective analysis of UGT1A1 promoter polymorphism for irinotecan dose escalation in metastatic colorectal cancer patients treated with bevacizumab plus FOLFIRI as the first-line setting: study protocol for a randomized controlled trial.
Colorectal Neoplasms
Prospective phase II trial of second-line FOLFIRI in patients with advanced colorectal cancer including analysis of UGT1A1 polymorphisms: FLIGHT 2 study.
Colorectal Neoplasms
Randomized Phase II Trial of CapOX plus Bevacizumab and CapIRI plus Bevacizumab as First-Line Treatment for Japanese Patients with Metastatic Colorectal Cancer (CCOG-1201 Study).
Colorectal Neoplasms
Rapid and sensitive detection of UGT1A1 polymorphisms associated with irinotecan toxicity by a novel DNA microarray.
Colorectal Neoplasms
Recommendations from the EGAPP Working Group: can UGT1A1 genotyping reduce morbidity and mortality in patients with metastatic colorectal cancer treated with irinotecan?
Colorectal Neoplasms
Refining the UGT1A Haplotype Associated with Irinotecan-Induced Hematological Toxicity in Metastatic Colorectal Cancer Patients Treated with 5-Fluorouracil/Irinotecan-Based Regimens.
Colorectal Neoplasms
Regimen Selection for First-line FOLFIRI and FOLFOX Based on UGT1A1 Genotype and Physical Background is Feasible in Japanese Patients with Advanced Colorectal Cancer.
Colorectal Neoplasms
Regorafenib plus FOLFIRI with irinotecan dose escalated according to uridine diphosphate glucuronosyltransferase 1A1 genotyping in patients with metastatic colorectal cancer.
Colorectal Neoplasms
Regorafenib plus FOLFIRI with irinotecan dose escalated according to uridine diphosphate glucuronosyltransferase 1A1genotyping in previous treated metastatic colorectal cancer patients:study protocol for a randomized controlled trial.
Colorectal Neoplasms
Regulation and expression of aberrant methylation on irinotecan metabolic genes CES2, UGT1A1 and GUSB in the in-vitro cultured colorectal cancer cells.
Colorectal Neoplasms
Regulation of UGT1A1 and HNF1 transcription factor gene expression by DNA methylation in colon cancer cells.
Colorectal Neoplasms
Relationship between the Expression of CES2, UGT1A1, and GUSB in colorectal cancer tissues and aberrant methylation.
Colorectal Neoplasms
Relationship between the expression of CES2, UGT1A1, and GUSB in colorectal cancer tissues and aberrant methylation.
Colorectal Neoplasms
Severe irinotecan-induced toxicity in a patient with UGT1A1 28 and UGT1A1 6 polymorphisms.
Colorectal Neoplasms
Single nucleotide polymorphisms of ABCC5 and ABCG1 transporter genes correlate to irinotecan-associated gastrointestinal toxicity in colorectal cancer patients: a DMET microarray profiling study.
Colorectal Neoplasms
Splice isoforms as therapeutic targets for colorectal cancer.
Colorectal Neoplasms
Sulforaphane suppresses carcinogenesis of colorectal cancer through the ERK/Nrf2?UDP glucuronosyltransferase 1A metabolic axis activation.
Colorectal Neoplasms
The coffee ingredients caffeic acid and caffeic acid phenylethyl ester protect against irinotecan-induced leukopenia and oxidative stress response.
Colorectal Neoplasms
The Correlation Between UGT1A1 Gene Phenotypes and the Clinical Prognosis of Advanced Colorectal Cancer After FOLFIRI Therapy.
Colorectal Neoplasms
The cost-effectiveness of UGT1A1 genotyping before colorectal cancer treatment with irinotecan from the perspective of the German statutory health insurance.
Colorectal Neoplasms
The effect of copy number variation in the phase II detoxification genes UGT2B17 and UGT2B28 on colorectal cancer risk.
Colorectal Neoplasms
The effect of UGT1A and UGT2B polymorphisms on colorectal cancer risk: haplotype associations and geneenvironment interactions.
Colorectal Neoplasms
UDP glucuronosyltransferase 1A expression levels determine the response of colorectal cancer cells to the heat shock protein 90 inhibitor ganetespib.
Colorectal Neoplasms
UDP-glucuronosyltransferase (UGT) 1A1*28 polymorphism-directed phase II study of irinotecan with 5'-deoxy-5-fluorouridine (5'-DFUR) for metastatic colorectal cancer.
Colorectal Neoplasms
UDP-glucuronosyltransferase 1A1*6 and *28 polymorphisms as indicators of initial dose level of irinotecan to reduce risk of neutropenia in patients receiving FOLFIRI for colorectal cancer.
Colorectal Neoplasms
UGT1A and TYMS genetic variants predict toxicity and response of colorectal cancer patients treated with first-line irinotecan and fluorouracil combination therapy.
Colorectal Neoplasms
UGT1A polymorphisms associated with worse outcome in colorectal cancer patients treated with irinotecan-based chemotherapy.
Colorectal Neoplasms
UGT1A1 6/28 polymorphisms could predict irinotecan-induced severe neutropenia not diarrhea in Chinese colorectal cancer patients.
Colorectal Neoplasms
UGT1A1 gene polymorphism is associated with toxicity and clinical efficacy of irinotecan-based chemotherapy in patients with advanced colorectal cancer.
Colorectal Neoplasms
UGT1A1 gene polymorphism: impact on toxicity and efficacy of irinotecan-based regimens in metastatic colorectal cancer.
Colorectal Neoplasms
UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancer.
Colorectal Neoplasms
UGT1A1 genotyping: a predictor of irinotecan-associated side effects and drug efficacy?
Colorectal Neoplasms
UGT1A1 Polymorphism for Irinotecan Dose Escalation in Patients with BRAF-Mutated Metastatic Colorectal Cancer Treated with First-Line Bevacizumab and FOLFIRI.
Colorectal Neoplasms
UGT1A1 polymorphisms and colorectal cancer susceptibility.
Colorectal Neoplasms
UGT1A1 predicts outcome in colorectal cancer treated with irinotecan and fluorouracil.
Colorectal Neoplasms
UGT1A1 regulatory variant with potential effect on efficacy of HIV and cancer drugs commonly prescribed in South Africa.
Colorectal Neoplasms
UGT1A1*28 genotype predicts gastrointestinal toxicity in patients treated with intermediate-dose irinotecan.
Colorectal Neoplasms
UGT1A1*6, 1A7*3, and 1A9*22 genotypes predict severe neutropenia in FOLFIRI-treated mCRC in two prospective studies in Japan.
Colorectal Neoplasms
UGT1A7 and UGT1A9 polymorphisms predict response and toxicity in colorectal cancer patients treated with capecitabine/irinotecan.
Colorectal Neoplasms
Understanding chemotherapy treatment pathways of advanced colorectal cancer patients to inform an economic evaluation in the United Kingdom.
Colorectal Neoplasms
Utility of Pretreatment Bilirubin Level and UGT1A1 Polymorphisms in Multivariate Predictive Models of Neutropenia Associated with Irinotecan Treatment in Previously Untreated Patients with Colorectal Cancer.
Colorectal Neoplasms
[Association between genetic polymorphisms of metabolic enzymes and susceptibility of colorectal cancer]
Colorectal Neoplasms
[Examination of UGT1A1 polymorphisms and irinotecan-induced neutropenia in patients with Colorectal cancer].
Colorectal Neoplasms
[Interest of UGT1A1 genotyping within digestive cancers treatment by irinotecan].
Colorectal Neoplasms
[Polymorphisms of UGT1A gene and irinotecan toxicity in Chinese colorectal cancer patients]
Congenital Hypothyroidism
Bilirubin uridine diphosphate glucuronosyltransferase hepatic activity in jaundice associated with congenital hypothyroidism.
Coronary Artery Disease
Is bilirubin a marker of vascular disease and/or cancer and is it a potential therapeutic target?
Coronary Artery Disease
Serum bilirubin levels, UGT1A1 polymorphisms and risk for coronary artery disease.
Coronary Artery Disease
UGT1A1 Promoter Genotype is not Strongly Associated With Severity of Coronary Artery Disease.
Coronary Artery Disease
UGT1A1 rs4148323 A Allele is Associated With Increased 2-Hydroxy Atorvastatin Formation and Higher Death Risk in Chinese Patients With Coronary Artery Disease.
COVID-19
Pharmacogenomics landscape of COVID-19 therapy response in Serbian population and comparison with worldwide populations.
COVID-19
[Clinical characteristics and influencing factors of patients with novel coronavirus pneumonia combined with liver injury in Shaanxi region].
Crigler-Najjar Syndrome
A case of anorexia nervosa with hyperbilirubinaemia in a patient homozygous for a mutation in the bilirubin UDP-glucuronosyltransferase gene.
Crigler-Najjar Syndrome
A case report of a novel 22?bp duplication within exon 1 of the UGT1A1 in a Sudanese infant with Crigler-Najjar syndrome type I.
Crigler-Najjar Syndrome
A new frame-shifting mutation of UGT1A1 gene causes type I Crigler-Najjar syndrome.
Crigler-Najjar Syndrome
A novel deletion with two pathogenic variants of UGT1A1 causing Crigler-Najjar syndrome in two unrelated Chinese.
Crigler-Najjar Syndrome
A novel intronic mutation results in the use of a cryptic splice acceptor site within the coding region of UGT1A1, causing Crigler-Najjar syndrome type 1.
Crigler-Najjar Syndrome
A novel missense mutation of the bilirubin UDP-glucuronosyltransferase gene in a Turkish patient with Crigler-Najjar syndrome type 1.
Crigler-Najjar Syndrome
A Novel Pathogenic UGT1A1 Variant in a Sudanese Child with Type 1 Crigler-Najjar Syndrome.
Crigler-Najjar Syndrome
A novel stop codon mutation in exon 1 (558C>A) of the UGT1A1 gene in a Thai neonate with Crigler-Najjar syndrome type I.
Crigler-Najjar Syndrome
A novel strategy for in vivo expansion of transplanted hepatocytes using preparative hepatic irradiation and FasL-induced hepatocellular apoptosis.
Crigler-Najjar Syndrome
A novel UGT1A1 gene mutation causing severe unconjugated hyperbilirubinemia: a case report.
Crigler-Najjar Syndrome
A Rare Case Report of Crigler Najjar Syndrome Type II.
Crigler-Najjar Syndrome
A rare UGT1A1 genotype causes Crigler-Najjar syndrome type 2 in a Caucasian boy.
Crigler-Najjar Syndrome
A translationally optimized AAV-UGT1A1 vector drives safe and long-lasting correction of Crigler-Najjar syndrome.
Crigler-Najjar Syndrome
Acute hepatitis in Crigler-Najjar syndrome.
Crigler-Najjar Syndrome
Adeno-associated viral vector serotype 5 poorly transduces liver in rat models.
Crigler-Najjar Syndrome
Analysis of bilirubin UDP-glucuronosyltransferase gene mutations in an unusual Crigler-Najjar syndrome patient.
Crigler-Najjar Syndrome
Bilirubin UDP-glucuronosyltransferase 1 is the only relevant bilirubin glucuronidating isoform in man.
Crigler-Najjar Syndrome
Biochemical and molecular aspects of genetic disorders of bilirubin metabolism.
Crigler-Najjar Syndrome
Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome.
Crigler-Najjar Syndrome
Co-occurrence of three different mutations in the bilirubin UDP-glucuronosyltransferase gene in a Chinese family with Crigler-Najjar syndrome type I and Gilbert's syndrome.
Crigler-Najjar Syndrome
Complete correction of hyperbilirubinemia in the Gunn rat model of Crigler-Najjar syndrome type I following transient in vivo adenovirus-mediated expression of human bilirubin UDP-glucuronosyltransferase.
Crigler-Najjar Syndrome
Compound heterozygosity of a novel exon 3 frameshift (p.R357P fs*24) mutation and Y486D mutation in exon 5 of the UGT1A1 gene in a Thai infant with Crigler-Najjar syndrome type 2.
Crigler-Najjar Syndrome
Conformational change of UGT1A1 by a novel missense mutation (p.L131P) causing Crigler-Najjar syndrome type I.
Crigler-Najjar Syndrome
Correction of congenital indirect hyperbilirubinemia by small intestinal transplantation.
Crigler-Najjar Syndrome
Correction of the UDP-glucuronosyltransferase gene defect in the gunn rat model of crigler-najjar syndrome type I with a chimeric oligonucleotide.
Crigler-Najjar Syndrome
CORRIGENDUM: Quantitative Systems Pharmacology Model of hUGT1A1-modRNA Encoding for the UGT1A1 Enzyme to Treat Crigler-Najjar Syndrome Type 1.
Crigler-Najjar Syndrome
Crigler-Najjar syndrome type 2: Novel UGT1A1 mutation.
Crigler-Najjar Syndrome
Crigler-Najjar syndrome type I in a Turkish newborn caused by a novel mutation and Gilbert type genetic defect.
Crigler-Najjar Syndrome
Crigler-Najjar Syndrome Type II Caused by a Homozygous Triple Mutation [T-3279G, A(TA)7TAA, and H39D] of UGT1A1.
Crigler-Najjar Syndrome
Crigler-Najjar Syndrome Type II Diagnosed in a Patient with Jaundice Since Birth.
Crigler-Najjar Syndrome
Crigler-Najjar syndrome type II is inherited both as a dominant and as a recessive trait.
Crigler-Najjar Syndrome
Crigler-Najjar syndrome: therapeutic options and consequences of mutations in the UGT1A1 complex.
Crigler-Najjar Syndrome
Diagnosis and management of Crigler-Najjar syndrome.
Crigler-Najjar Syndrome
Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II.
Crigler-Najjar Syndrome
Disease burden of Crigler-Najjar syndrome: systematic review and future perspectives.
Crigler-Najjar Syndrome
Disruption of HNF1? binding site causes inherited severe unconjugated hyperbilirubinemia.
Crigler-Najjar Syndrome
Ex Vivo Lentivirus Transduction and Immediate Transplantation of Uncultured Hepatocytes for Treating Hyperbilirubinemic Gunn Rat.
Crigler-Najjar Syndrome
Frequencies of A(TA)(7)TAA, G71R, and G493R Mutations of the UGT1A1 Gene in the Malaysian Population.
Crigler-Najjar Syndrome
Functional characterization of hepatocytes for cell transplantation: customized cell preparation for each receptor.
Crigler-Najjar Syndrome
Gene mapping of human bilirubin UDP-glucuronosyl transferase on 1q21-q23 by a cell sorter and in situ hybridization.
Crigler-Najjar Syndrome
Gene Replacement Therapy for Genetic Hepatocellular Jaundice.
Crigler-Najjar Syndrome
Gene symbol: UGT1A1. Disease: Crigler-Najjar syndrome 1.
Crigler-Najjar Syndrome
Generation of Ugt1-deficient murine liver cell lines using TALEN technology.
Crigler-Najjar Syndrome
Genes and Pathways Promoting Long-Term Liver Repopulation by Ex Vivo hYAP-ERT2 Transduced Hepatocytes and Treatment of Jaundice in Gunn Rats.
Crigler-Najjar Syndrome
Genetic factors in neonatal hyperbilirubinemia and kernicterus.
Crigler-Najjar Syndrome
Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects.
Crigler-Najjar Syndrome
Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome.
Crigler-Najjar Syndrome
Gilbert and Crigler Najjar syndromes: An update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database.
Crigler-Najjar Syndrome
Gilbert syndrome with systemic lupus erythematosus presenting with persistent unconjugated hyperbilirubinemia: A case report.
Crigler-Najjar Syndrome
Glucuronidation of 3'-azido-3'-deoxythymidine in human liver microsomes: enzyme inhibition by drugs and steroid hormones.
Crigler-Najjar Syndrome
Hepatic Parenchymal Injury in Crigler-Najjar Type I.
Crigler-Najjar Syndrome
Hereditary spherocytosis coexisting with UDP-glucuronosyltransferase deficiency highly suggestive of Crigler-Najjar syndrome type II.
Crigler-Najjar Syndrome
Human liver stem cells express UGT1A1 and improve phenotype of immunocompromised Crigler Najjar syndrome type I mice.
Crigler-Najjar Syndrome
Identification of a genetic alteration in the code for bilirubin UDP-glucuronosyltransferase in the UGT1 gene complex of a Crigler-Najjar type I patient.
Crigler-Najjar Syndrome
Identification of a novel deletion in UDP-glucuronosyltransferase gene in a patient with Crigler-Najjar syndrome type I.
Crigler-Najjar Syndrome
Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from Slovakia.
Crigler-Najjar Syndrome
Immunochemical analysis of uridine diphosphate-glucuronosyltransferase in four patients with the Crigler-Najjar syndrome type I.
Crigler-Najjar Syndrome
Improved efficacy and reduced toxicity by ultrasound-guided intrahepatic injections of helper-dependent adenoviral vector in gunn rats.
Crigler-Najjar Syndrome
Influence of mutations associated with Gilbert and Crigler-Najjar type II syndromes on the glucuronidation kinetics of bilirubin and other UDP-glucuronosyltransferase 1A substrates.
Crigler-Najjar Syndrome
Intestinal excretion of unconjugated bilirubin in man and rats with inherited unconjugated hyperbilirubinemia.
Crigler-Najjar Syndrome
Investigation of the molecular basis of the genetic deficiency of UDP-glucuronosyltransferase in Crigler-Najjar syndrome.
Crigler-Najjar Syndrome
Isolated hepatocyte transplantation for Crigler-Najjar syndrome type 1.
Crigler-Najjar Syndrome
Kernicterus in an adult who is heterozygous for Crigler-Najjar syndrome and homozygous for Gilbert-type genetic defect.
Crigler-Najjar Syndrome
Life-long correction of hyperbilirubinemia with a neonatal liver-specific AAV-mediated gene transfer in a lethal mouse model of Crigler-Najjar Syndrome.
Crigler-Najjar Syndrome
Linkage disequilibrium of UGT1A1 *6 and UGT1A1 *28 in relation to UGT1A6 and UGT1A7 polymorphisms.
Crigler-Najjar Syndrome
Liver irradiation: a potential preparative regimen for hepatocyte transplantation.
Crigler-Najjar Syndrome
Management of Crigler-Najjar syndrome.
Crigler-Najjar Syndrome
Marked endogenous activation of the CYP1A1 and CYP1A2 genes in the congenitally jaundiced Gunn rat.
Crigler-Najjar Syndrome
Mechanisms of inherited deficiencies of multiple UDP-glucuronosyltransferase isoforms in two patients with Crigler-Najjar syndrome, type I.
Crigler-Najjar Syndrome
Meta-analysis diagnostic accuracy of SNP-based pathogenicity detection tools: a case of UTG1A1 gene mutations.
Crigler-Najjar Syndrome
Molecular Analysis of the UGT1A1 Gene in Korean Patients with Crigler-Najjar Syndrome Type II.
Crigler-Najjar Syndrome
Mutation of UGT1A1 gene in a case of Crigler-Najjar syndrome type II.
Crigler-Najjar Syndrome
Nonviral gene transfer into liver and muscle for treatment of hyperbilirubinemia in the gunn rat.
Crigler-Najjar Syndrome
Novel human pathological mutations. Gene symbol: UGT1A1. Disease: Crigler-Najjar syndrome 1.
Crigler-Najjar Syndrome
p.Cys223Tyr mutation causing Crigler-Najjar syndrome type II.
Crigler-Najjar Syndrome
Paternal isodisomy for chromosome 2 as the cause of Crigler-Najjar type I syndrome.
Crigler-Najjar Syndrome
Persistent jaundice in an infant with homozygous beta thalassemia due to co-inherited Crigler-Najjar syndrome.
Crigler-Najjar Syndrome
Polymorphism of UDP-glucuronosyltransferase and drug metabolism.
Crigler-Najjar Syndrome
Prenatal diagnosis of bilirubin-UDP-glucuronosyltransferase deficiency in rats by genomic DNA analysis.
Crigler-Najjar Syndrome
Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate- glucuronosyltransferase gene.
Crigler-Najjar Syndrome
Quantitative Systems Pharmacology Model of hUGT1A1-modRNA Encoding for the UGT1A1 Enzyme to Treat Crigler-Najjar Syndrome Type 1.
Crigler-Najjar Syndrome
Rapid proteasomal degradation of translocation-deficient UDP-glucuronosyltransferase 1A1 proteins in patients with Crigler-Najjar type II.
Crigler-Najjar Syndrome
Reduction of hyperbilirubinemia with hypericum extract (St. John's Wort) in a patient with Crigler-Najjar syndrome type II.
Crigler-Najjar Syndrome
Removal of protein-bound and unbound unconjugated bilirubin by perfusion of plasma through an anion-exchange resin in a case of Crigler-Najjar syndrome type I.
Crigler-Najjar Syndrome
Retrovirus-mediated expression of HUG Br1 in Crigler-Najjar syndrome type I human fibroblasts and correction of the genetic defect in Gunn rat hepatocytes.
Crigler-Najjar Syndrome
Role of a homozygous A(TA)7TAA promoter polymorphism and an exon 1 heterozygous frameshift mutation UGT1A1 in Crigler-Najjar syndrome type II in a Thai neonate.
Crigler-Najjar Syndrome
Spectrum of UGT1A1 variants in Pakistani children affected with inherited unconjugated hyperbilirubinemias.
Crigler-Najjar Syndrome
Spectrum of UGT1A1 Variations in Chinese Patients with Crigler-Najjar Syndrome Type II.
Crigler-Najjar Syndrome
Stimulation of transcriptional expression of human UDP-glucuronosyltransferase 1A1 by dexamethasone.
Crigler-Najjar Syndrome
Sustained Reduction of Hyperbilirubinemia in Gunn Rats after Adeno-Associated Virus-Mediated Gene Transfer of Bilirubin UDP-Glucuronosyltransferase Isozyme 1A1 to Skeletal Muscle.
Crigler-Najjar Syndrome
The anesthetic implications of Crigler-Najjar syndrome.
Crigler-Najjar Syndrome
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.
Crigler-Najjar Syndrome
Three Japanese patients with Crigler-Najjar syndrome type I carry an identical nonsense mutation in the gene for UDP-glucuronosyltransferase.
Crigler-Najjar Syndrome
Treatment of Crigler-Najjar type 1 disease: relevance of early liver transplantation.
Crigler-Najjar Syndrome
Truncated UDP-glucuronosyltransferase (UGT) from a Crigler-Najjar syndrome type II patient colocalizes with intact UGT in the endoplasmic reticulum.
Crigler-Najjar Syndrome
Two Different UGT1A1 Mutations causing Crigler-Najjar Syndrome types I and II in an Iranian Family.
Crigler-Najjar Syndrome
Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome.
Crigler-Najjar Syndrome
Two unrelated patients with rare Crigler-Najjar syndrome type I: two novel mutations and a patient with loss of heterozygosity of UGT1A1 gene.
Crigler-Najjar Syndrome
Type I crigler najjar syndrome in Tunisia: a study of 30 cases.
Crigler-Najjar Syndrome
UGT1A1 gene mutation due to Crigler-Najjar syndrome in Iranian patients: identification of a novel mutation.
Crigler-Najjar Syndrome
UGT1A1 Gene Mutations in Pakistani Children Suffering from Inherited Nonhemolytic Unconjugated Hyperbilirubinemias.
Crigler-Najjar Syndrome
UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children: A retrospective analysis and quantitative correlation.
Crigler-Najjar Syndrome
UGT1A1 polymorphisms in cancer: impact on irinotecan treatment.
Crigler-Najjar Syndrome
UGT1A1 Variants c.864+5G>T and c.996+2_996+5del of a Crigler-Najjar Patient Induce Aberrant Splicing in Minigene Assays.
Crigler-Najjar Syndrome
UGT1A1(TA)n promoter polymorphism--a new case of a (TA)8 allele in Caucasians.
Crigler-Najjar Syndrome
Ultrasound-guided in Utero Transplantation of Placental Stem Cells into the Liver of Crigler-Najjar Syndrome Model Rat.
Crigler-Najjar Syndrome
Update on a previously reported missense mutation: The c.1160 C>A mutation in the UGT1A1 gene result in Crigler-Najjar syndrome type 1.
Crigler-Najjar Syndrome
[Analysis of mutation site characteristics of Gilbert syndrome and Crigler--Najjar syndrome in relation to uridine diphosphate glucuronosyltransferase A1 gene].
Crigler-Najjar Syndrome
[Crigler-Najjar syndrome. Report of one case with a long term follow up].
Crigler-Najjar Syndrome
[Genetic analysis of a child affected with Crigler-Najjar syndrome type II].
Crigler-Najjar Syndrome
[Genetic defect of the hyperbilirubinemic Gunn rat, a model for Crigler-Najjar syndrome type I]
Crigler-Najjar Syndrome
[Gilbert disease and type I and II Crigler-Najjar syndrome due to mutations in the same UGT1A1 gene locus]
Crohn Disease
A functional polymorphism in UGT1A1 related to hyperbilirubinemia is associated with a decreased risk for Crohn's disease.
Cystic Fibrosis
Coinheritance of Gilbert syndrome-associated UGT1A1 mutation increases gallstone risk in cystic fibrosis.
Cystic Fibrosis
Enhanced hepatic drug clearance in patients with cystic fibrosis.
Dehydration
Role of extrahepatic UDP-glucuronosyltransferase 1A1: Advances in understanding breast milk-induced neonatal hyperbilirubinemia.
Dermatitis, Atopic
Predicting therapy response to mycophenolic acid using UGT1A9 genotyping: towards personalized medicine in atopic dermatitis.
Diabetes Mellitus
A model-based approach to analyze the influence of UGT2B15 polymorphism driven pharmacokinetic differences on the pharmacodynamic response of the PPAR agonist sipoglitazar.
Diabetes Mellitus
Dapagliflozin Inhibits Cell Adhesion to Collagen I and IV and Increases Ectodomain Proteolytic Cleavage of DDR1 by Increasing ADAM10 Activity.
Diabetes Mellitus
Diabetes mellitus reduces activity of human UDP-glucuronosyltransferase 2B7 in liver and kidney leading to decreased formation of mycophenolic acid acyl-glucuronide metabolite.
Diabetes Mellitus, Type 2
A model-based approach to analyze the influence of UGT2B15 polymorphism driven pharmacokinetic differences on the pharmacodynamic response of the PPAR agonist sipoglitazar.
Diabetes Mellitus, Type 2
Dapagliflozin Inhibits Cell Adhesion to Collagen I and IV and Increases Ectodomain Proteolytic Cleavage of DDR1 by Increasing ADAM10 Activity.
Diabetes Mellitus, Type 2
Evaluation of the Impact of UGT Polymorphism on the Pharmacokinetics and Pharmacodynamics of the Novel PPAR Agonist Sipoglitazar.
Digestive System Neoplasms
Genetic polymorphisms of the uridine diphosphate glucuronosyltransferase 1A7 and colorectal cancer risk in relation to cigarette smoking and alcohol drinking in a Chinese population.
dihydropyrimidinase deficiency
Predictive and prognostic biomarkers with therapeutic targets in breast, colorectal, and non-small cell lung cancers: A systemic review of current development, evidence, and recommendation.
dihydropyrimidinase deficiency
[Pharmacogenetics of anti-cancer drugs]
dihydropyrimidinase deficiency
[Prerequisites to the administration and prevention of adverse effects of chemotherapy in colorectal cancer]
Dihydropyrimidine Dehydrogenase Deficiency
Predictive and prognostic biomarkers with therapeutic targets in breast, colorectal, and non-small cell lung cancers: A systemic review of current development, evidence, and recommendation.
Dihydropyrimidine Dehydrogenase Deficiency
[Pharmacogenetics of anti-cancer drugs]
Dihydropyrimidine Dehydrogenase Deficiency
[Prerequisites to the administration and prevention of adverse effects of chemotherapy in colorectal cancer]
Drug Resistant Epilepsy
Influence of uridine diphosphate glucuronosyltransferase inducers and inhibitors on the plasma lamotrigine concentration in pediatric patients with refractory epilepsy.
Drug-Related Side Effects and Adverse Reactions
Association of UGT2B7 and ABCB1 genotypes with morphine-induced adverse drug reactions in Japanese patients with cancer.
Drug-Related Side Effects and Adverse Reactions
Clinical implications of UGT1A1*28 genotype testing in colorectal cancer patients.
Drug-Related Side Effects and Adverse Reactions
Establishment of the experimental procedure for prediction of conjugation capacity in mutant UGT1A1.
Drug-Related Side Effects and Adverse Reactions
Genetic Association of Drug Response to Erlotinib in Chinese Advanced Non-small Cell Lung Cancer Patients.
Drug-Related Side Effects and Adverse Reactions
Inhibition of human and rabbit liver steroid and xenobiotic UDP-glucuronosyltransferases by tertiary amine drugs--implications for adverse drug reactions.
Drug-Related Side Effects and Adverse Reactions
Neobavaisoflavone Induces Bilirubin Metabolizing Enzyme UGT1A1 via PPAR? and PPAR?.
Drug-Related Side Effects and Adverse Reactions
Novel personalized medicine technology: UGT1A1 testing for irinotecan as a case study.
Drug-Related Side Effects and Adverse Reactions
Pharmacogenetics and pediatric cancer.
Drug-Related Side Effects and Adverse Reactions
Polymorphism of UDP-glucuronosyltransferase and drug metabolism.
Drug-Related Side Effects and Adverse Reactions
Prevalence of clinically relevant UGT1A alleles and haplotypes in African populations.
Drug-Related Side Effects and Adverse Reactions
Recommendations from the EGAPP Working Group: can UGT1A1 genotyping reduce morbidity and mortality in patients with metastatic colorectal cancer treated with irinotecan?
Drug-Related Side Effects and Adverse Reactions
Uridine diphosphate glucuronosyltransferase 1A1.
Dwarfism
Glycosylation of inositol phosphorylceramide sphingolipids is required for normal growth and reproduction in Arabidopsis.
Elephantiasis, Filarial
Intestinal UDP-glucuronosyltransferase as a potential target for the treatment and prevention of lymphatic filariasis.
Endometrial Neoplasms
Disturbed expression of phase I and phase II estrogen-metabolizing enzymes in endometrial cancer: Lower levels of CYP1B1 and increased expression of S-COMT.
Endometrial Neoplasms
Efficacy of combination chemotherapy using irinotecan and nedaplatin for patients with recurrent and refractory endometrial carcinomas: preliminary analysis and literature review.
Endometrial Neoplasms
Function of UDP-glucuronosyltransferase 2B17 (UGT2B17) is involved in endometrial cancer.
Endometrial Neoplasms
Genetic variations in UGT1A1 and UGT2B7 and endometrial cancer risk.
Endometrial Neoplasms
Short heterodimer partner (SHP) orphan nuclear receptor inhibits the transcriptional activity of aryl hydrocarbon receptor (AHR)/AHR nuclear translocator (ARNT).
Endometrial Neoplasms
The function of uterine UDP-glucuronosyltransferase 1A8 (UGT1A8) and UDP-glucuronosyltransferase 2B7 (UGT2B7) is involved in endometrial cancer based on estrogen metabolism regulation.
Endometrial Neoplasms
The functional UGT1A1 promoter polymorphism decreases endometrial cancer risk.
Endometrial Neoplasms
UGT1A1 Genetic Polymorphisms, Endogenous Estrogen Exposure, Soy Food Intake, and Endometrial Cancer Risk.
Endometriosis
Enhanced UGT1A1 Gene and Protein Expression in Endometriotic Lesions.
Endometriosis
Whole exome sequencing identifies hemizygous deletions in the UGT2B28 and USP17L2 genes in a three?generation family with endometriosis.
Enterocolitis, Necrotizing
Humanized UGT1 Mice, Regulation of UGT1A1, and the Role of the Intestinal Tract in Neonatal Hyperbilirubinemia and Breast Milk-Induced Jaundice.
Epilepsy
Association of SCN1A, SCN2A, and UGT2B7 Polymorphisms with Responsiveness to Valproic Acid in the Treatment of Epilepsy.
Epilepsy
Association of UGT2B7 and CaMK4 with response of valproic acid in Chinese children with epilepsy.
Epilepsy
Correlation of the UGT1A4 gene polymorphism with serum concentration and therapeutic efficacy of lamotrigine in Han Chinese of Northern China.
Epilepsy
Effect of CYP2C19, UGT1A8, and UGT2B7 on valproic acid clearance in children with epilepsy: a population pharmacokinetic model.
Epilepsy
Effect of UGT2B7 genetic variants on serum valproic acid concentration.
Epilepsy
Effect of UGT2B7 genotypes on plasma concentration of valproic acid: a meta-analysis.
Epilepsy
Effects of ABCB1, ABCC2, UGT2B7 and HNF4? genetic polymorphisms on oxcarbazepine concentrations and therapeutic efficacy in patients with epilepsy.
Epilepsy
Effects of Comedication and Genetic Factors on the Population Pharmacokinetics of Lamotrigine: A Prospective Analysis in Chinese Patients With Epilepsy.
Epilepsy
Effects of UGT1A4 genetic polymorphisms on serum lamotrigine concentrations in Chinese children with epilepsy.
Epilepsy
Effects of UGT1A6 and GABRA1 on Standardized Valproic Acid Plasma Concentrations and Treatment Effect in Children With Epilepsy in China.
Epilepsy
Effects of UGT1A6, UGT2B7, and CYP2C9 genotypes on plasma concentrations of valproic acid in Chinese children with epilepsy.
Epilepsy
Effects of UGT1A9 genetic polymorphisms on monohydroxylated derivative of oxcarbazepine concentrations and oxcarbazepine monotherapeutic efficacy in Chinese patients with epilepsy.
Epilepsy
Glomerular filtration rate is a major predictor of clearance of oxcarbazepine active metabolite in adult Chinese epileptic patients: A population pharmacokinetic analysis.
Epilepsy
Impact of Age and Genotype on Serum Concentrations of Valproic Acid and Its Hepatotoxic Metabolites in Chinese Pediatric Patients with Epilepsy.
Epilepsy
Influence of genetic variants and antiepileptic drug co-treatment on lamotrigine plasma concentration in Mexican Mestizo patients with epilepsy.
Epilepsy
Influence of UDP-glucuronosyltransferase polymorphisms on valproic acid pharmacokinetics in Chinese epilepsy patients.
Epilepsy
Influence of Uridine Diphosphate Glucuronosyltransferase 2B7 -161C>T Polymorphism on the Concentration of Valproic Acid in Pediatric Epilepsy Patients.
Epilepsy
Polymorphisms of ABCG2, ABCB1 and HNF4? are associated with Lamotrigine trough concentrations in epilepsy patients.
Epilepsy
Prevalence of UGT1A6 polymorphisms in children with epilepsy on valproate monotherapy.
Epilepsy
The Effect of Uridine Diphosphate Glucuronosyltransferase (UGT)1A6 Genetic Polymorphism on Valproic Acid Pharmacokinetics in Indian Patients with Epilepsy: A Pharmacogenetic Approach.
Epilepsy
The influence of UGT2B7 genotype on valproic acid pharmacokinetics in Chinese epilepsy patients.
Epilepsy
The relationship between UGT1A4 polymorphism and serum concentration of lamotrigine in patients with epilepsy.
Epilepsy
UGT polymorphisms and lamotrigine clearance during pregnancy.
Epilepsy
[Effect of UGT1A6 genetic polymorphisms on the metabolism of sodium valproate]
Esophageal Neoplasms
Associations between UGT1A1*6/*28 polymorphisms and irinotecan-induced severe toxicity in Chinese gastric or esophageal cancer patients.
Esophageal Neoplasms
High enzyme activity UGT1A1 or low activity UGT1A8 and UGT2B4 genotypes increase esophageal cancer risk.
Esophageal Squamous Cell Carcinoma
Germline copy number loss of UGT2B28 and gain of PLEC contribute to increased human esophageal squamous cell carcinoma risk in Southwest China.
Esophageal Squamous Cell Carcinoma
High enzyme activity UGT1A1 or low activity UGT1A8 and UGT2B4 genotypes increase esophageal cancer risk.
Exanthema
No association between non-bullous skin reactions from lamotrigine and heterozygosity of UGT1A4 genetic variants *2(P24T) or *3(L48V) in Norwegian patients.
Fascioliasis
Antihepatotoxic properties of uridine-diphosphoglucose in liver fluke infection. Experimental fascioliasis in the rat.
Fascioliasis
Fasciola hepatica: liver enzymes in rats and interaction with chemical inducers.
Fascioliasis
Participation of lipid peroxidation in the loss of hepatic drug-metabolizing activities in experimental fascioliasis in the rat.
Fatty Liver
Genome-wide analysis of hepatic lipid content in extreme obesity.
Fatty Liver
Hepatic and extrahepatic glucuronidation of bile acids in man. Characterization of bile acid uridine 5'-diphosphate-glucuronosyltransferase in hepatic, renal, and intestinal microsomes.
Fatty Liver
Validated liquid chromatography-tandem mass spectrometry method for determination of totally nine probe metabolites of cytochrome P450 enzymes and UDP-glucuronosyltransferases.
Febrile Neutropenia
Long-term Survival in a Patient with Small-cell Lung Cancer Undergoing Hemodialysis Who Received Multiple Courses of Chemotherapy.
Febrile Neutropenia
Phase II study of a triplet regimen of S-1 combined with irinotecan and oxaliplatin in patients with metastatic gastric cancer: clinical and pharmacogenetic results.
Fetal Growth Retardation
Circulating mRNAs are differentially expressed in pregnancies with severe placental insufficiency and at high risk of stillbirth.
Focal Nodular Hyperplasia
Differential down-regulation of the UDP-glucuronosyltransferase 1A locus is an early event in human liver and biliary cancer.
Follicular Cyst
Association between liver failure and hepatic UDP-glucuronosyltransferase activity in dairy cows with follicular cysts.
Gallbladder Diseases
Genome-wide association meta-analysis for total serum bilirubin levels.
Gallbladder Diseases
UGT1A1 promoter polymorphisms and the development of hyperbilirubinemia and gallbladder disease in children with sickle cell anemia.
Gallstones
A high frequency of Gilbert syndrome (UGT1A1*28/*28) and associated hyperbilirubinemia but not cholelithiasis in adolescent and adult north Indian patients with transfusion-dependent ?-thalassemia.
Gallstones
Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis.
Gallstones
Coinheritance of Gilbert syndrome-associated UGT1A1 mutation increases gallstone risk in cystic fibrosis.
Gallstones
Dissecting the genetic heterogeneity of gallbladder stone formation.
Gallstones
Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis?
Gallstones
Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1.
Gallstones
Genetics of biliary lithiasis from an ethnic perspective.
Gallstones
Genome-wide association meta-analysis for total serum bilirubin levels.
Gallstones
Gilbert Syndrome as a Predisposing Factor for Cholelithiasis Risk in the Greek Adult Population.
Gallstones
Gilbert syndrome as a predisposing factor for cholelithiasis risk in the Greek adult population.
Gallstones
Gilbert's syndrome as a predisposing factor for idiopathic cholelithiasis in children.
Gallstones
Hereditary spherocytosis coexisting with UDP-glucuronosyltransferase deficiency highly suggestive of Crigler-Najjar syndrome type II.
Gallstones
Identification of UDP glycosyltransferase 3A1 as a UDP N-acetylglucosaminyltransferase.
Gallstones
Implication of genetic variation at the promoter and exon1 of UGT1A1 in occurrence of cholelithiasis in Tunisia.
Gallstones
Incidence and Risk of Gallstone Disease in Gilbert's Syndrome Patients in Indian Population.
Gallstones
Influence of bilirubin uridine diphosphate-glucuronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in children with sickle cell anemia.
Gallstones
Loci From a Genome-Wide Analysis of Bilirubin Levels Are Associated With Gallstone Risk and Composition.
Gallstones
Pathogenesis of cholesterol and pigment gallstones: An update.
Gallstones
Possible role of a defect in hepatic bilirubin glucuronidation in the initiation of cholesterol gallstones.
Gallstones
Pyrimidine-5'-nucleotidase Campinas, a new mutation (p.R56G) in the NT5C3 gene associated with pyrimidine-5'-nucleotidase type I deficiency and influence of Gilbert's Syndrome on clinical expression.
Gallstones
Serum Total Bilirubin, not Cholelithiasis, is Influenced by UGT1A1 Polymorphism, Alpha Thalassemia and ?(s) Haplotype: First Report on Comparison between Arab-Indian and African ?(s) Genes.
Gallstones
Thalassemia minor, the Gilbert mutation, and the risk of gallstones.
Gallstones
The linear effects of alpha-thalassaemia, the UGT1A1 and HMOX1 polymorphisms on cholelithiasis in sickle cell disease.
Gallstones
UGT1A promoter polymorphisms influence bilirubin response to hydroxyurea therapy in sickle cell anemia.
Gallstones
UGT1A1 promoter polymorphism associated with serum bilirubin level in Saudi patients with sickle cell disease.
Gallstones
UGT1A1 variation and gallstone formation in sickle cell disease.
Gallstones
Uridine diphosphate glucuronosyl transferase 1A (UGT1A1) promoter polymorphism in young patients with sickle cell anaemia: report of the first cohort study from Nigeria.
Gallstones
[Effects of Shengqing Capsules on cholelithiasis-related genes in guinea pigs]
Gastritis
The Implication of the Polymorphisms of COX-1, UGT1A6, and CYP2C9 among Cardiovascular Disease (CVD) Patients Treated with Aspirin.
Gastrointestinal Neoplasms
Clinical Assessment of 5-Fluorouracil/Leucovorin, Nab-Paclitaxel, and Irinotecan (FOLFIRABRAX) in Untreated Patients with Gastrointestinal Cancer Using UGT1A1 Genotype-Guided Dosing.
Gastrointestinal Neoplasms
UGT1A1 Gene Polymorphisms and the Toxicities of FOLFIRI in Chinese Han Patients with Gastrointestinal Cancer.
Gastrointestinal Neoplasms
UGT1A7 polymorphisms in chronic pancreatitis: an example of genotyping pitfalls.
Gastrointestinal Stromal Tumors
Imatinib-induced hyperbilirubinemia with UGT1A1 (*28) promoter polymorphism: first case series in patients with gastrointestinal stromal tumor.
Genetic Diseases, Inborn
Generation of Ugt1-deficient murine liver cell lines using TALEN technology.
Genetic Diseases, Inborn
Therapeutic lentivirus-mediated neonatal in vivo gene therapy in hyperbilirubinemic Gunn rats.
Genetic Diseases, Inborn
Tyrosine kinase inhibitor resistance: a case report on chronic myeloid leukemia and Gilbert's syndrome.
Genetic Diseases, Inborn
[Crigler-Najjar syndrome. Report of one case with a long term follow up].
Gilbert Disease
''Iatrogenic Gilbert syndrome''- A strategy for reducing vascular and cancer risk by increasing plasma unconjugated bilirubin.
Gilbert Disease
(TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome.
Gilbert Disease
5-Fluorouracil/irinotecan induced lethal toxicity as a result of a combined pharmacogenetic syndrome: report of a case.
Gilbert Disease
A case of anorexia nervosa with hyperbilirubinaemia in a patient homozygous for a mutation in the bilirubin UDP-glucuronosyltransferase gene.
Gilbert Disease
A Case of hereditary spherocytosis coexisting with Gilbert's syndrome.
Gilbert Disease
A clinical PCR fragment analysis assay for TA repeat sizing in the UGT1A1 promoter region.
Gilbert Disease
A functional polymorphism in UGT1A1 related to hyperbilirubinemia is associated with a decreased risk for Crohn's disease.
Gilbert Disease
A Gilbert's syndrome UGT1A1 variant confers susceptibility to tranilast-induced hyperbilirubinemia.
Gilbert Disease
A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome.
Gilbert Disease
A new case of (TA)8 allele in the UGT1A1 gene promoter in a Caucasian girl with Gilbert syndrome.
Gilbert Disease
A Novel ?-Spectrin Pathogenic Variant in Trans to ?-Spectrin LELY Causing Neonatal Jaundice With Hemolytic Anemia From Hereditary Pyropoikilocytosis Coexisting With Gilbert Syndrome.
Gilbert Disease
Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome.
Gilbert Disease
Association of human liver bilirubin UDP-glucuronyltransferase activity with a polymorphism in the promoter region of the UGT1A1 gene.
Gilbert Disease
Bilirubin conjugation, reflected by conjugated bilirubin fractions, in glucose-6-phosphate dehydrogenase-deficient neonates: a determining factor in the pathogenesis of hyperbilirubinemia.
Gilbert Disease
Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome.
Gilbert Disease
Bilirubin, platelet activation and heart disease: A missing link to cardiovascular protection in Gilbert's syndrome?
Gilbert Disease
Bilirubin, renal hemodynamics, and blood pressure.
Gilbert Disease
Caloric intake and unconjugated hyperbilirubinemia.
Gilbert Disease
Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome.
Gilbert Disease
Chronic persistent hepatitis and unconjugated hyperbilirubinemia.
Gilbert Disease
Clinical UGT1A1 Genetic Analysis in Pediatric Patients: Experience of a Reference Laboratory.
Gilbert Disease
Clozapine metabolism may be affected by Gilbert's syndrome: case report and discussion.
Gilbert Disease
Co-occurrence of three different mutations in the bilirubin UDP-glucuronosyltransferase gene in a Chinese family with Crigler-Najjar syndrome type I and Gilbert's syndrome.
Gilbert Disease
Coexistence of Gilbert syndrome with hereditary haemolytic anaemias.
Gilbert Disease
Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis.
Gilbert Disease
Coinheritance of Gilbert syndrome-associated UGT1A1 mutation increases gallstone risk in cystic fibrosis.
Gilbert Disease
Combined effect of regulatory polymorphisms on transcription of UGT1A1 as a cause of Gilbert syndrome.
Gilbert Disease
Combined test for UGT1A1 -3279T-->G and A(TA)nTAA polymorphisms best predicts Gilbert's syndrome in Italian pediatric patients.
Gilbert Disease
Combined UGT1A1 and UGT1A7 variant alleles are associated with increased risk of Gilbert's syndrome in Taiwanese adults.
Gilbert Disease
Compound heterozygous UGT1A1*28 and UGT1A1*6 or single homozygous UGT1A1*28 are major genotypes associated with Gilbert's syndrome in Chinese Han people.
Gilbert Disease
Contribution of UGT1A1 variations to chemotherapy-induced unconjugated hyperbilirubinemia in pediatric leukemia patients.
Gilbert Disease
Correlation between the UDP-glucuronosyltransferase (UGT1A1) TATAA box polymorphism and carcinogen detoxification phenotype: significantly decreased glucuronidating activity against benzo(a)pyrene-7,8-dihydrodiol(-) in liver microsomes from subjects with the UGT1A1*28 variant.
Gilbert Disease
Correlation of mutational analysis to clinical features in Taiwanese patients with Gilbert's syndrome.
Gilbert Disease
Correlation of UGT1A1 TATA-box polymorphism and jaundice in breastfed newborns-early presentation of Gilbert's syndrome.
Gilbert Disease
Crigler-Najjar syndrome in Saudi Arabia.
Gilbert Disease
Determinants of iron status and bilirubin levels in congenital dyserythropoietic anaemia type I.
Gilbert Disease
Development of a new DHPLC assay for genotyping UGT1A (TA)n polymorphism associated with Gilbert's syndrome.
Gilbert Disease
Development of icterus gravis in a preterm infant with G71R UGT1A1 polymorphism.
Gilbert Disease
Developmental hyperbilirubinemia and CNS toxicity in mice humanized with the UDP glucuronosyltransferase 1 (UGT1) locus.
Gilbert Disease
Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II.
Gilbert Disease
Differing pathogenesis of perinatal bilirubinemia in glucose-6-phosphate dehydrogenase-deficient versus-normal neonates.
Gilbert Disease
Disposition of propafenone in a poor metabolizer of CYP2D6 with Gilbert's syndrome.
Gilbert Disease
DNA base bulge vs unmatched end formation in probe-based diagnostic insertion/deletion genotyping: genotyping the UGT1A1 (TA)(n) polymorphism by real-time fluorescence PCR.
Gilbert Disease
Drug-mediated toxicity caused by genetic deficiency of UDP-glucuronosyltransferases.
Gilbert Disease
Dual hereditary jaundice: simultaneous occurrence of mutations causing Gilbert's and Dubin-Johnson syndrome.
Gilbert Disease
Dual polymorphisms in UDP-glucuronosyltransferases 1A1 and 1A6: a novel mechanism for hyperserotoninaemia in Gilbert's syndrome mimicking carcinoid syndrome?
Gilbert Disease
Effect of bilirubin UDP glucuronosyltransferase 1 gene TATA box genotypes on serum bilirubin concentrations in chronic liver injuries.
Gilbert Disease
Effect of splenectomy of hepatic bilirubin clearance in patients with hereditary spherocytosis. Implications for the diagnosis of Gilbert's syndrome.
Gilbert Disease
Effect of UDP-glucuronosyltransferase 1A1 activity on risk for developing Gilbert's syndrome.
Gilbert Disease
Effects of variation status and enzyme activity for UDP-glucuronosyltransferase 1A1 gene on neonatal hyperbilirubinemia.
Gilbert Disease
Evidence for a gene influencing serum bilirubin on chromosome 2q telomere: a genomewide scan in the Framingham study.
Gilbert Disease
Expression and inducibility of the human bilirubin UDP-glucuronosyltransferase UGT1A1 in liver and cultured primary hepatocytes: evidence for both genetic and environmental influences.
Gilbert Disease
FEATURES OF GILBERT'S SYNDROME IN PATIENTS WITH DIFFERENT GENOTYPES UGT1AI.
Gilbert Disease
Frequencies of A(TA)(7)TAA, G71R, and G493R Mutations of the UGT1A1 Gene in the Malaysian Population.
Gilbert Disease
Frequencies of UDP-glucuronosyltransferase 1 (UGT1A1) gene promoter polymorphisms among distinct ethnic groups from Brazil.
Gilbert Disease
Frequent co-occurrence of the TATA box mutation associated with Gilbert's syndrome (UGT1A1*28) with other polymorphisms of the UDP-glucuronosyltransferase-1 locus (UGT1A6*2 and UGT1A7*3) in Caucasians and Egyptians.
Gilbert Disease
Function, genetic polymorphism, and transcriptional regulation of human UDP-glucuronosyltransferase (UGT) 1A1.
Gilbert Disease
Gene mapping of human bilirubin UDP-glucuronosyl transferase on 1q21-q23 by a cell sorter and in situ hybridization.
Gilbert Disease
Gene Replacement Therapy for Genetic Hepatocellular Jaundice.
Gilbert Disease
Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias.
Gilbert Disease
Genetic interactions in the pathogenesis of neonatal hyperbilirubinemia: Gilbert's Syndrome and glucose-6-phosphate dehydrogenase deficiency.
Gilbert Disease
Genetic lesions in the UGT1A1 genes among Gilbert's syndrome patients from India.
Gilbert Disease
Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype.
Gilbert Disease
Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects.
Gilbert Disease
Genetic predisposition to the metabolism of irinotecan (CPT-11). Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes.
Gilbert Disease
Genetic variation in UGT1A1 typical of Gilbert syndrome is associated with unconjugated hyperbilirubinemia in patients receiving tocilizumab.
Gilbert Disease
Genetic variation underlying common hereditary hyperbilirubinaemia (Gilbert's syndrome) and respiratory health in the 1946 British birth cohort.
Gilbert Disease
Genetics of biliary lithiasis from an ethnic perspective.
Gilbert Disease
Genotype frequencies of UDP-glucuronosyltransferase 1A1 promoter gene polymorphism in the population of healthy Croatian pre-scholars.
Gilbert Disease
Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome.
Gilbert Disease
Gilbert and Crigler Najjar syndromes: An update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database.
Gilbert Disease
Gilbert syndrome accelerates development of neonatal jaundice.
Gilbert Disease
Gilbert Syndrome as a Predisposing Factor for Cholelithiasis Risk in the Greek Adult Population.
Gilbert Disease
Gilbert syndrome as a predisposing factor for cholelithiasis risk in the Greek adult population.
Gilbert Disease
Gilbert syndrome caused by a homozygous missense mutation (Tyr486Asp) of bilirubin UDP-glucuronosyltransferase gene.
Gilbert Disease
Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia.
Gilbert Disease
Gilbert syndrome with systemic lupus erythematosus presenting with persistent unconjugated hyperbilirubinemia: A case report.
Gilbert Disease
Gilbert syndrome.
Gilbert Disease
Gilbert syndrome: analysis of the promoter region of the uridine diphosphate-glucuronosyltransferase 1 gene in the Greek population.
Gilbert Disease
Gilbert's disease and atazanavir: from phenotype to UDP-glucuronosyltransferase haplotype.
Gilbert Disease
Gilbert's syndrome and hyperbilirubinemia in protease inhibitor therapy--an extended haplotype of genetic variants increases risk in indinavir treatment.
Gilbert Disease
Gilbert's Syndrome and Irinotecan Toxicity: Combination with UDP-Glucuronosyltransferase 1A7 Variants Increases Risk.
Gilbert Disease
Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates.
Gilbert Disease
Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn.
Gilbert Disease
Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase.
Gilbert Disease
Gilbert's syndrome is not associated with HELLP syndrome.
Gilbert Disease
Gilbert's syndrome: High frequency of the (TA) (7) TAA allele in India and its interaction with a novel CAT insertion in promoter of the gene for bilirubin UDP-glucuronosyltransferase 1 gene.
Gilbert Disease
Glutathione S-transferase, cytochrome P450, and uridine 5'-diphosphate-glucuronosyltransferase in human small intestine and liver.
Gilbert Disease
Hemolysis and bilirubin conjugation in association with UDP-glucuronosyltransferase 1A1 promoter polymorphism.
Gilbert Disease
Hepatic bilirubin and UDP-glucuronate levels in Bolivian squirrel monkeys exhibiting fasting hyperbilirubinemia.
Gilbert Disease
Hepatic uptake of organic anions affects the plasma bilirubin level in subjects with Gilbert's syndrome mutations in UGT1A1.
Gilbert Disease
Hereditary spherocytosis coexisting with UDP-glucuronosyltransferase deficiency highly suggestive of Crigler-Najjar syndrome type II.
Gilbert Disease
Human UDP-glucuronosyltransferases: metabolism, expression, and disease.
Gilbert Disease
Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome.
Gilbert Disease
Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia.
Gilbert Disease
Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects.
Gilbert Disease
In vitro UGT1A1 inhibition by tyrosine kinase inhibitors and association with drug-induced hyperbilirubinemia.
Gilbert Disease
Incidence and Risk of Gallstone Disease in Gilbert's Syndrome Patients in Indian Population.
Gilbert Disease
Induction of mild hyperbilirubinemia: Hype or real therapeutic opportunity?
Gilbert Disease
Influence of mutations associated with Gilbert and Crigler-Najjar type II syndromes on the glucuronidation kinetics of bilirubin and other UDP-glucuronosyltransferase 1A substrates.
Gilbert Disease
Influence of UGT1A1 promoter polymorphism, ?-thalassemia and ?s haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort.
Gilbert Disease
Inheritance of hyperbilirubinemia: evidence for a major autosomal recessive gene.
Gilbert Disease
Irinotecan treatment in cancer patients with UGT1A1 polymorphisms.
Gilbert Disease
Is Gilbert Syndrome a new risk factor for breast cancer?
Gilbert Disease
Jaundice with hypertrophic pyloric stenosis as an early manifestation of Gilbert syndrome.
Gilbert Disease
Kernicterus in an adult who is heterozygous for Crigler-Najjar syndrome and homozygous for Gilbert-type genetic defect.
Gilbert Disease
Linkage between A(TA)7TAA and -3279T>G mutations in UGT1A1 is not essential for pathogenesis of Gilbert syndrome.
Gilbert Disease
Linkage disequilibrium of UGT1A1 *6 and UGT1A1 *28 in relation to UGT1A6 and UGT1A7 polymorphisms.
Gilbert Disease
Loci From a Genome-Wide Analysis of Bilirubin Levels Are Associated With Gallstone Risk and Composition.
Gilbert Disease
Low glucose-6-phosphate dehydrogenase enzyme activity level at the time of hemolysis in a male neonate with the African type of deficiency.
Gilbert Disease
Mechanism of indinavir-induced hyperbilirubinemia.
Gilbert Disease
Melting temperature assay for a UGT1A gene variant in Gilbert syndrome.
Gilbert Disease
Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects.
Gilbert Disease
Molecular pathogenesis of Gilbert's syndrome: decreased TATA-binding protein binding affinity of UGT1A1 gene promoter.
Gilbert Disease
Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes.
Gilbert Disease
Multiple variants in UGT1A1 gene are factors to develop indirect hyper-bilirubinemia.
Gilbert Disease
Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese.
Gilbert Disease
Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene: the common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese.
Gilbert Disease
Neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient heterozygotes.
Gilbert Disease
Non tumoral hyperserotoninaemia responsive to octreotide due to dual polymorphism in UGT1A1 and UGT1A6.
Gilbert Disease
Novel missense mutation of the UGT1A1 gene in Thai siblings with Gilbert's syndrome.
Gilbert Disease
Oncology Drug Dosing in Gilbert Syndrome Associated with UGT1A1: A Summary of the Literature.
Gilbert Disease
Outcome and toxicities associated to chemotherapy in children with acute lymphoblastic leukemia and Gilbert syndrome. Usefulness of UGT1A1 mutational screening.
Gilbert Disease
Pazopanib-induced hyperbilirubinemia is associated with Gilbert's syndrome UGT1A1 polymorphism.
Gilbert Disease
Pegvisomant-Induced Cholestatic Hepatitis in an Acromegalic Patient with UGT1A1?(?)?28 Mutation.
Gilbert Disease
Perfluorocarbons and Gilbert syndrome (phenotype) in the C8 Health Study Population.
Gilbert Disease
Persistent unconjugated hyperbilirubinemia after liver transplantation due to an abnormal bilirubin UDP-glucuronosyltransferase gene promoter sequence in the donor.
Gilbert Disease
Persisting hyperbilirubinemia in patients with paroxysmal nocturnal hemoglobinuria (PNH) chronically treated with eculizumab: The role of hepatocanalicular transporter variants.
Gilbert Disease
Pharmacogenetics of anticancer agents: lessons from amonafide and irinotecan.
Gilbert Disease
Pharmacogenetics: a tool for individualizing antineoplastic therapy.
Gilbert Disease
Phenotype-genotype correlation of in vitro SN-38 (active metabolite of irinotecan) and bilirubin glucuronidation in human liver tissue with UGT1A1 promoter polymorphism.
Gilbert Disease
Polymorphism of UDP-glucuronosyltransferase and drug metabolism.
Gilbert Disease
Polymorphisms in UDP glucuronosyltransferase genes: functional consequences and clinical relevance.
Gilbert Disease
Prediction of irinotecan and 5-fluorouracil toxicity and response in patients with advanced colorectal cancer.
Gilbert Disease
Preparation of reference material for UGT1A1 (TA)n polymorphism genotyping.
Gilbert Disease
Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate- glucuronosyltransferase gene.
Gilbert Disease
Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism?
Gilbert Disease
Rapid molecular diagnosis of the Gilbert's syndrome-associated exon 1 mutation within the UGT1A1 gene.
Gilbert Disease
Rapid UGT1A1 (TA)(n) genotyping by high resolution melting curve analysis for Gilbert's syndrome diagnosis.
Gilbert Disease
Rare TA repeats in promoter TATA box of the UDP glucuronosyltranferase (UGT1A1) gene in Croatian subjects.
Gilbert Disease
Regulation of bilirubin glucuronide synthesis in primate (Macaca fascicularis) liver. Kinetic analysis of microsomal bilirubin uridine diphosphate glucuronyltransferase.
Gilbert Disease
Relevance of different UGT1A1 polymorphisms in irinotecan-induced toxicity: a molecular and clinical study of 75 patients.
Gilbert Disease
Restriction fragment length polymorphism effectively identifies exon 1 mutation of UGT1A1 gene in patients with Gilbert's Syndrome.
Gilbert Disease
Role of bilirubin overproduction in revealing Gilbert's syndrome: is dyserythropoiesis an important factor?
Gilbert Disease
Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients.
Gilbert Disease
Role of UGT1A1 and ADH gene polymorphisms in pegvisomant-induced liver toxicity in acromegalic patients.
Gilbert Disease
Role of UGT1A1 mutation in fasting hyperbilirubinemia.
Gilbert Disease
Serum bilirubin may serve as a marker for increased heme oxygenase activity and inducibility in tissues - A rationale for the versatile health protection associated with elevated plasma bilirubin.
Gilbert Disease
Severe jaundice in a patient with a previously undescribed glucose-6-phosphate dehydrogenase (G6PD) mutation and Gilbert syndrome.
Gilbert Disease
Severe Neonatal Hyperbilirubinemia and UGT1A1 Promoter Polymorphism.
Gilbert Disease
Single-step identification of all length polymorphisms in the UGT1A1 gene promoter.
Gilbert Disease
Snapback Primer Genotyping of the Gilbert Syndrome UGT1A1 (TA)n Promoter Polymorphism by High-Resolution Melting.
Gilbert Disease
Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlation.
Gilbert Disease
Spectrum of UGT1A1 variants in Pakistani children affected with inherited unconjugated hyperbilirubinemias.
Gilbert Disease
Stimulation of transcriptional expression of human UDP-glucuronosyltransferase 1A1 by dexamethasone.
Gilbert Disease
TaqMan real time PCR for the Detection of the Gilbert's Syndrome Markers UGT1A1*28; UGT1A1*36 and UGT1A1*37.
Gilbert Disease
Targeted therapy of cancer: new roles for pathologists in colorectal cancer.
Gilbert Disease
TATA-box mutant in the promoter of the uridine diphosphate glucuronosyltransferase gene in Italian patients with Gilbert's syndrome.
Gilbert Disease
The Association between Prolonged Jaundice and UGT1A1 Gene Polymorphism (G71R) in Gilbert's Syndrome.
Gilbert Disease
The combination of new missense mutation with [A(TA)7TAA] dinucleotide repeat in UGT1A1 gene promoter causes Gilbert's syndrome.
Gilbert Disease
The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency.
Gilbert Disease
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.
Gilbert Disease
The novel bilirubin/phenol UDP-glucuronosyltransferase UGT1 gene locus: implications for multiple nonhemolytic familial hyperbilirubinemia phenotypes.
Gilbert Disease
The polymorphism c.-3279T>G in the phenobarbital-responsive enhancer module of the bilirubin UDP-glucuronosyltransferase gene is associated with Gilbert syndrome.
Gilbert Disease
Three-dimensional polyacrylamide gel-based DNA microarray method effectively identifies UDP-glucuronosyltransferase 1A1 gene polymorphisms for the correct diagnosis of Gilbert's syndrome.
Gilbert Disease
Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome.
Gilbert Disease
Tyrosine kinase inhibitor resistance: a case report on chronic myeloid leukemia and Gilbert's syndrome.
Gilbert Disease
UDP-glucuronosyltransferase in Gilbert's syndrome.
Gilbert Disease
UGT1A1 (TA)n Promoter Genotype: Diagnostic and Population Pharmacogenetic Marker in Serbia.
Gilbert Disease
UGT1A1 dysfunction increases liver burden and aggravates hepatocyte damage caused by long-term bilirubin metabolism disorder.
Gilbert Disease
UGT1A1 gene linkage analysis: application of polymorphic markers rs4148326/rs4124874 in the Iranian population.
Gilbert Disease
UGT1A1 Gene Mutations in Pakistani Children Suffering from Inherited Nonhemolytic Unconjugated Hyperbilirubinemias.
Gilbert Disease
UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children: A retrospective analysis and quantitative correlation.
Gilbert Disease
UGT1A1 polymorphism and hyperbilirubinemia in a patient who received sorafenib.
Gilbert Disease
UGT1A1 polymorphisms in cancer: impact on irinotecan treatment.
Gilbert Disease
UGT1A1(TA)n promoter polymorphism--a new case of a (TA)8 allele in Caucasians.
Gilbert Disease
UGT1A1*28 relationship with abnormal total bilirubin levels in chronic hepatitis C patients: Outcomes from a case-control study.
Gilbert Disease
Use of double gradient denaturing gradient gel electrophoresis to detect (AT)n polymorphisms in the UDP-glucuronosyltransferase 1 gene promoter associated with Gilbert's syndrome.
Gilbert Disease
Use of fully denaturing HPLC for UGT1A1 genotyping in Gilbert syndrome.
Gilbert Disease
Variation in UGT1A1 activity in Gilbert's syndrome.
Gilbert Disease
What is Gilbert's syndrome? Lesson from genetic polymorphisms of UGT1A1 in Gilbert's syndrome from Asia.
Gilbert Disease
[A case of Gilbert syndrome caused by UGT1A1 gene compound heterozygous mutations].
Gilbert Disease
[A study of polymorphism in UDP-glucuronosyltransferase 1 (UGT-1A1) promoter gene in Korean patients with Gilbert's syndrome]
Gilbert Disease
[Analysis of diagnostic value of UGT1A1 gene detection in Gilbert syndrome].
Gilbert Disease
[Analysis of mutation site characteristics of Gilbert syndrome and Crigler--Najjar syndrome in relation to uridine diphosphate glucuronosyltransferase A1 gene].
Gilbert Disease
[Anesthesia in a patient with Gilbert's syndrome: case report.]
Gilbert Disease
[Clinical Characteristics and Gene Mutations of Gilbert Syndrome Complicated with Myeloproliferative Neoplasm].
Gilbert Disease
[From gene to disease; unconjugated hyperbilirubinemia: Gilbert's syndrome and Crigler-Najjar types I and II]
Gilbert Disease
[Genetic analysis of the UGT1A1 gene mutation sites in a Chinese family suffered from Gilbert's syndrome]
Gilbert Disease
[Gilbert disease and type I and II Crigler-Najjar syndrome due to mutations in the same UGT1A1 gene locus]
Gilbert Disease
[Inherited disorders of bilirubin metabolism]
Gilbert Disease
[Molecular diagnosis of heritable unconjugated hyperbilirubinemias]
Gilbert Disease
[Pharmacogenetics of anti-cancer drugs]
Gilbert Disease
[Polymorphisms of the UDP-glucuronosyltransferase 1-A1 gene in Tunisian population].
Gilbert Disease
[Repeated yellowing of the skin and sclera for 2 years].
Gilbert Disease
[The heterogeneity of paracetamol metabolism in Gilbert's disease]
Glioblastoma
Dopamine is an aryl hydrocarbon receptor agonist.
Glioma
A phase 1 trial of intravenous liposomal irinotecan in patients with recurrent high-grade glioma.
Glioma
Irinotecan therapy in a 12-year-old girl with recurrent brain stem glioma and without functional polymorphisms in UGT1A1 activity: case report.
Glomerulonephritis
Effects of uridine diphosphate glucuronosyltransferase 2B7 and 1A7 pharmacogenomics and patient clinical parameters on steady-state mycophenolic acid pharmacokinetics in glomerulonephritis.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Bilirubin conjugation, reflected by conjugated bilirubin fractions, in glucose-6-phosphate dehydrogenase-deficient neonates: a determining factor in the pathogenesis of hyperbilirubinemia.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Clinical and genetic risk factors for moderate hyperbilirubinemia in Brazilian newborn infants.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Clinical Significance of UGT1A1 Genetic Analysis in Chinese Neonates with Severe Hyperbilirubinemia.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Coinheritance of variant UDP-glucuronosyl transferase 1A1 gene and glucose-6-phosphate dehydrogenase deficiency in adults with hyperbilirubinemia.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Effects of variant UDP-glucuronosyltransferase 1A1 gene, glucose-6-phosphate dehydrogenase deficiency and thalassemia on cholelithiasis.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Genetic factors related to unconjugated hyperbilirubinemia amongst adults.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Genetic polymorphisms in Thai neonates with hyperbilirubinemia.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Molecular genetics of unconjugated hyperbilirubinemia in Taiwanese.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Prevalence of UGT1A1 (TA)n promoter polymorphism in Panamanians neonates with G6PD deficiency.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Risk assessment of gene variants for neonatal hyperbilirubinemia in Taiwan.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
Risk of Hyperbilirubinemia in Breast-Fed Infants.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
UGT1A1 Genetic Analysis as a Diagnostic Aid for Individuals with Unconjugated Hyperbilirubinemia.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
[Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert syndrome]
glucose-6-phosphate dehydrogenase (nadp+) deficiency
[Role of genetic factors in occurrence of neonatal jaundice in Guangxi region]
Glucosephosphate Dehydrogenase Deficiency
Clinical and genetic risk factors for moderate hyperbilirubinemia in Brazilian newborn infants.
Glucosephosphate Dehydrogenase Deficiency
Clinical Significance of UGT1A1 Genetic Analysis in Chinese Neonates with Severe Hyperbilirubinemia.
Glucosephosphate Dehydrogenase Deficiency
Coinheritance of variant UDP-glucuronosyl transferase 1A1 gene and glucose-6-phosphate dehydrogenase deficiency in adults with hyperbilirubinemia.
Glucosephosphate Dehydrogenase Deficiency
Effects of variant UDP-glucuronosyltransferase 1A1 gene, glucose-6-phosphate dehydrogenase deficiency and thalassemia on cholelithiasis.
Glucosephosphate Dehydrogenase Deficiency
Genetic factors related to unconjugated hyperbilirubinemia amongst adults.
Glucosephosphate Dehydrogenase Deficiency
Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia.
Glucosephosphate Dehydrogenase Deficiency
Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study.
Glucosephosphate Dehydrogenase Deficiency
Molecular genetics of unconjugated hyperbilirubinemia in Taiwanese.
Glucosephosphate Dehydrogenase Deficiency
Prevalence of UGT1A1 (TA)n promoter polymorphism in Panamanians neonates with G6PD deficiency.
Glucosephosphate Dehydrogenase Deficiency
Risk assessment of gene variants for neonatal hyperbilirubinemia in Taiwan.
Glucosephosphate Dehydrogenase Deficiency
Risk of Hyperbilirubinemia in Breast-Fed Infants.
Glucosephosphate Dehydrogenase Deficiency
The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency.
Glucosephosphate Dehydrogenase Deficiency
UGT1A1 Genetic Analysis as a Diagnostic Aid for Individuals with Unconjugated Hyperbilirubinemia.
Glucosephosphate Dehydrogenase Deficiency
[Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert syndrome]
glucuronosyltransferase deficiency
A novel UGT1A1 gene mutation causing severe unconjugated hyperbilirubinemia: a case report.
glucuronosyltransferase deficiency
Acute hepatitis in Crigler-Najjar syndrome.
glucuronosyltransferase deficiency
Adeno-associated viral vector serotype 5 poorly transduces liver in rat models.
glucuronosyltransferase deficiency
Adeno-associated virus vector serotypes mediate sustained correction of bilirubin UDP glucuronosyltransferase deficiency in rats.
glucuronosyltransferase deficiency
Adenovirus-mediated gene therapy to restore expression and functionality of multiple UDP-glucuronosyltransferase 1A enzymes in Gunn rat liver.
glucuronosyltransferase deficiency
Auxiliary liver transplantation in jaundiced rats with UDP-glucuronyltransferase deficiency and defective hepatobiliary transport.
glucuronosyltransferase deficiency
cDNA cloning and characterization of feline CYP1A1 and CYP1A2.
glucuronosyltransferase deficiency
Developmental, Genetic, Dietary, and Xenobiotic Influences on Neonatal Hyperbilirubinemia.
glucuronosyltransferase deficiency
Disease burden of Crigler-Najjar syndrome: systematic review and future perspectives.
glucuronosyltransferase deficiency
DPD and UGT1A1 deficiency in colorectal cancer patients receiving triplet chemotherapy with fluoropyrimidines, oxaliplatin and irinotecan.
glucuronosyltransferase deficiency
Efficacy and safety of rifampicin in patients with persistent hepatocellular secretory failure.
glucuronosyltransferase deficiency
Genetic diagnosis and pathogenic analysis of an atypical hereditary spherocytosis combined with UGT1A1 partial deficiency: A case report.
glucuronosyltransferase deficiency
Gilbert and Crigler Najjar syndromes: An update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database.
glucuronosyltransferase deficiency
Hereditary spherocytosis coexisting with UDP-glucuronosyltransferase deficiency highly suggestive of Crigler-Najjar syndrome type II.
glucuronosyltransferase deficiency
Hereditary spherocytosis in 3 children coexisting with UDP-glucuronyl transferase 1A1 deficiency.
glucuronosyltransferase deficiency
Management of Crigler-Najjar syndrome.
glucuronosyltransferase deficiency
Mycophenolate Mofetil impairs transduction of single-stranded adeno-associated viral vectors.
glucuronosyltransferase deficiency
Pharmacogenetics of irinotecan: clinical perspectives on the utility of genotyping.
glucuronosyltransferase deficiency
Phenol UDP-glucuronosyltransferase deficiency in Gunn rats: mRNA levels are considerably reduced.
glucuronosyltransferase deficiency
Phosphofructokinase deficiency (Tarui disease) associated with hepatic glucuronyltransferase deficiency (Gilbert's syndrome): a case and family study.
glucuronosyltransferase deficiency
Role of cysteine residues in the function of human UDP glucuronosyltransferase isoform 1A1 (UGT1A1).
glucuronosyltransferase deficiency
Successful treatment of UGT1A1 deficiency in a rat model of Crigler-Najjar disease by intravenous administration of a liver-specific lentiviral vector.
glucuronosyltransferase deficiency
The 3-methylcholanthrene-inducible UDP-glucuronosyltransferase deficiency in the hyperbilirubinemic rat (Gunn rat) is caused by a -1 frameshift mutation.
glucuronosyltransferase deficiency
The activity of 1-naphthol-UDP-glucuronosyltransferase in the brain.
glucuronosyltransferase deficiency
Thyroid hormones and the hepatic handling of bilirubin. II. Effects of hypothyroidism and hyperthyroidism on the apparent maximal biliary secretion of bilirubin in the Wistar rat.
glucuronosyltransferase deficiency
UDP-glucuronyltransferase-catalyzed deconjugation of bilirubin monoglucuronide.
glucuronosyltransferase deficiency
UDPglucuronosyltransferase deficiency in man and animals.
glucuronosyltransferase deficiency
UGT1A1 dysfunction increases liver burden and aggravates hepatocyte damage caused by long-term bilirubin metabolism disorder.
glucuronosyltransferase deficiency
[Chronic cholemia caused by a hepatic glucuronyltransferase deficiency in adults]
glucuronosyltransferase deficiency
[Interest of UGT1A1 genotyping within digestive cancers treatment by irinotecan].
Glycogen Storage Disease
Improved preparation of hepatic microsomes for in vitro diagnosis of inherited disorders of the glucose-6-phosphatase system.
Gout
Main contribution of UGT1A1 and CYP2C9 in the metabolism of UR-1102, a novel agent for the treatment of gout.
Graft vs Host Disease
A single minor histocompatibility antigen encoded by UGT2B17 and presented by human leukocyte antigen-A*2902 and -B*4403.
Graft vs Host Disease
A UGT2B17-positive donor is a risk factor for higher transplant-related mortality and lower survival after bone marrow transplantation.
Head and Neck Neoplasms
Combined effect of genetic polymorphisms in phase I and II biotransformation enzymes on head and neck cancer risk.
Head and Neck Neoplasms
Genetic polymorphism in the conjugating enzyme UGT1A1 and the risk of head and neck cancer.
Head and Neck Neoplasms
Genetic polymorphisms in the tobacco smoke carcinogens detoxifying enzyme UGT1A7 and the risk of head and neck cancer.
Head and Neck Neoplasms
Interactions Among Genetic Variants in Tobacco Metabolizing Genes and Smoking Are Associated with Head and Neck Cancer Susceptibility in North Indians.
Head and Neck Neoplasms
Polymorphisms in CYP2A13 and UGT1A7 genes and head and neck cancer susceptibility in North Indians.
Heart Diseases
Evaluation of effects of polymorphism for metabolic enzymes on pharmacokinetics of carvedilol by population pharmacokinetic analysis.
Heart Diseases
Polymorphisms in genes encoding acetylsalicylic acid metabolizing enzymes are unrelated to upper gastrointestinal health in cardiovascular patients on acetylsalicylic acid.
Heart Failure
Relation of ADRB1, CYP2D6, and UGT1A1 polymorphisms with dose of, and response to, carvedilol or metoprolol therapy in patients with chronic heart failure.
Heart Failure
Stereoselective Glucuronidation of Carvedilol in Human Liver and Intestinal Microsomes.
Heart Failure
Stereoselective metabolism of racemic carvedilol by UGT1A1 and UGT2B7, and effects of mutation of these enzymes on glucuronidation activity.
HELLP Syndrome
[Refinement and role of the diagnosis of Gilbert disease with molecular biology]
Hemochromatosis
Coexistence of HFE and rare UGT1A1 genes mutations in patients with iron overload related liver injury.
Hemochromatosis
UGT1A1 gene polymorphism as a potential factor inducing iron overload in the pathogenesis of type 1 hereditary hemochromatosis.
Hemoglobinopathies
The effect of UGT1A1 promoter polymorphism in the development of hyperbilirubinemia and cholelithiasis in hemoglobinopathy patients.
Hemoglobinopathies
The effect of UGT1A1 promoter polymorphism on bilirubin response to hydroxyurea therapy in hemoglobinopathies.
Hepatic Insufficiency
Enhancement of intestinal UDP-glucuronosyltranferase activity in partially hepatectomized rats.
Hepatic Insufficiency
The impact of serotonergic system dysfunction on the regulation of P4501A isoforms during liver insufficiency and consequences for thyroid hormone homeostasis.
Hepatitis
Chronic persistent hepatitis and unconjugated hyperbilirubinemia.
Hepatitis
Diclofenac covalent protein binding is dependent on acyl glucuronide formation and is inversely related to P450-mediated acute cell injury in cultured rat hepatocytes.
Hepatitis
Hepatic and extrahepatic glucuronidation of bile acids in man. Characterization of bile acid uridine 5'-diphosphate-glucuronosyltransferase in hepatic, renal, and intestinal microsomes.
Hepatitis
Impact of edaphic factors and nutrient management on the hepatoprotective efficiency of Carlinoside purified from pigeon pea leaves: An evaluation of UGT1A1 activity in hepatitis induced organelles.
Hepatitis
Increase of UDP-glucuronosyltransferase activities toward xenobiotics during the development of hereditary hepatitis in LEC rats.
Hepatitis
Regorafenib induced severe toxic hepatitis: characterization and discussion.
Hepatitis
[Gene mutation pattern of Gilbert's syndrome combined with viral hepatitis and its relationship with the exploration of clinical data].
Hepatitis
[Regulation of mRNA expression of human UDP-glucuronosyltransferase in hepatitis and liver cirrhosis patients]
Hepatitis
[Role of farnesoid X receptor in rats with acute cholestatic hepatitis].
Hepatitis B
Ages of hepatocellular carcinoma occurrence and life expectancy are associated with a UGT2B28 genomic variation.
Hepatitis B
Correlations between polymorphisms in the uridine diphosphate-glucuronosyltransferase 1A and C-C motif chemokine receptor 5 genes and infection with the hepatitis B virus in three ethnic groups in China.
Hepatitis B
UDP-glucuronosyltransferase 1A7 genetic polymorphisms are associated with hepatocellular carcinoma risk and onset age.
Hepatitis B
UDP-glucuronosyltransferase 1A7 polymorphisms are associated with liver cirrhosis.
Hepatitis B
UGT1A7 haplotype is associated with an increased risk of hepatocellular carcinoma in hepatitis B carriers.
Hepatitis B
UGT2B28 genomic variation is associated with hepatitis B e-antigen seroconversion in response to antiviral therapy.
Hepatitis B, Chronic
UGT1A7 haplotype is associated with an increased risk of hepatocellular carcinoma in hepatitis B carriers.
Hepatitis C
Characterization of autoantibodies against uridine-diphosphate glucuronosyltransferase in patients with inflammatory liver diseases.
Hepatitis C
Increased incidence of anti-LKM autoantibodies in a consecutive cohort of hepatitis C patients from central Greece.
Hepatitis C
Personalized medicine: Factors influencing reimbursement.
Hepatitis C
UDP-glucuronosyltransferase 1A7 genetic polymorphisms are associated with hepatocellular carcinoma in japanese patients with hepatitis C virus infection.
Hepatitis C
UDP-glucuronosyltransferase 1A7 genetic polymorphisms are associated with hepatocellular carcinoma risk and onset age.
Hepatitis C
UDP-glucuronosyltransferase 1A7 polymorphisms are associated with liver cirrhosis.
Hepatitis C, Chronic
Effect of nuclear receptor downregulation on hepatic expression of cytochrome P450 and transporters in chronic hepatitis C in association with fibrosis development.
Hepatitis C, Chronic
No association of promoter variations of HMOX1 and UGT1A1 genes with liver injury in chronic hepatitis C.
Hepatitis C, Chronic
UGT1A1*28 relationship with abnormal total bilirubin levels in chronic hepatitis C patients: Outcomes from a case-control study.
Hepatitis, Autoimmune
Autoantibodies against CYP2D6 and other drug-metabolizing enzymes in autoimmune hepatitis type 2.
Hepatitis, Autoimmune
Characterization of autoantibodies against uridine-diphosphate glucuronosyltransferase in patients with inflammatory liver diseases.
Hepatitis, Autoimmune
The N-terminal of human UGT1A6 is on the outside, as evidenced by ELISA with autoantibody in autoimmune hepatitis sera.
Hepatitis, Chronic
Chronic persistent hepatitis and unconjugated hyperbilirubinemia.
Hepatoblastoma
FXR induces the UGT2B4 enzyme in hepatocytes: a potential mechanism of negative feedback control of FXR activity.
Hepatoblastoma
Peroxisome proliferator-activated receptor alpha induces hepatic expression of the human bile acid glucuronidating UDP-glucuronosyltransferase 2B4 enzyme.
Hepatomegaly
Toxicological approach for elucidation of clobazam-induced hepatomegaly in male rats.
Herpes Zoster
Targeted salmon gene array (SalArray): a toxicogenomic tool for gene expression profiling of interactions between estrogen and aryl hydrocarbon receptor signalling pathways.
Hodgkin Disease
Pharmacogenetic study in Hodgkin's lymphomas reveals the impact of UGT1A1 polymorphisms on patient's prognosis.
Hodgkin Disease
Polymorphisms in genes encoding interleukin-10 and drug metabolizing enzymes GSTP1, GSTT1, GSTA1 and UGT1A1 influence risk and outcome in Hodgkin lymphoma.
Hyperandrogenism
Array-CGH detection of UGT2B28 gene deletion in a girl with primary amenorrhea and hyperandrogenism.
Hyperandrogenism
Frequencies of the D85 and Y85 variants of UGT2B15 in children and adolescent girls with hyperandrogenism.
Hyperbilirubinemia, Neonatal
211 G to A variation of UGT1A1 and severe neonatal hyperbilirubinemia.
Hyperbilirubinemia, Neonatal
A difference in mortality between two strains of jaundiced rats.
Hyperbilirubinemia, Neonatal
Association between neonatal hyperbilirubinemia and UDP-glucuronosyltransferase 1A1 gene polymorphisms.
Hyperbilirubinemia, Neonatal
Association between the Specific UGT1A1 Promoter Sequence Variant (c-3279T>G) and Unconjugated Neonatal Hyperbilirubinemia.
Hyperbilirubinemia, Neonatal
Association between UGT 1A1 Gly71Arg (G71R) polymorphism and neonatal hyperbilirubinemia.
Hyperbilirubinemia, Neonatal
Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feeding.
Hyperbilirubinemia, Neonatal
Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms.
Hyperbilirubinemia, Neonatal
Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism.
Hyperbilirubinemia, Neonatal
Association of Neonatal Hyperbilirubinemia with UGT1A1 Gene Polymorphisms: A Meta-Analysis.
Hyperbilirubinemia, Neonatal
Association of neonatal hyperbilirubinemia with uridine diphosphate-glucuronosyltransferase 1A1 gene polymorphisms: a meta-analysis.
Hyperbilirubinemia, Neonatal
Association of UGT1A1 variants and hyperbilirubinemia in breast-fed full-term Chinese infants.
Hyperbilirubinemia, Neonatal
Case-controlled study on indirect hyperbilirubinemia in exclusively breast fed neonates and mutations of the bilirubin Uridine Diphosphate-Glucuronyl transferase gene 1A1.
Hyperbilirubinemia, Neonatal
Clinical and pharmacogenetic factors affecting neonatal bilirubinemia following atazanavir treatment of mothers during pregnancy.
Hyperbilirubinemia, Neonatal
Clinical UGT1A1 Genetic Analysis in Pediatric Patients: Experience of a Reference Laboratory.
Hyperbilirubinemia, Neonatal
Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonates.
Hyperbilirubinemia, Neonatal
Cord blood bilirubin level in relation to bilirubin UDP-glucuronosyltransferase gene missense allele in Chinese neonates.
Hyperbilirubinemia, Neonatal
Correlation between UGT1A1 polymorphism and neonatal hyperbilirubinemia of neonates in Wuhan.
Hyperbilirubinemia, Neonatal
Developmental onset of bilirubin-induced neurotoxicity involves Toll-like receptor 2-dependent signaling in humanized UDP-glucuronosyltransferase1 mice.
Hyperbilirubinemia, Neonatal
Effects of Gly71Arg mutation in UGT1A1 gene on neonatal hyperbilirubinemia: a systematic review and meta-analysis.
Hyperbilirubinemia, Neonatal
Effects of variation status and enzyme activity for UDP-glucuronosyltransferase 1A1 gene on neonatal hyperbilirubinemia.
Hyperbilirubinemia, Neonatal
G71R mutation of the UGT1A1 gene is not associated with neonatal hyperbilirubinemia in India.
Hyperbilirubinemia, Neonatal
Genetic Factors and Delayed TSB Monitoring and Treatment as Risk Factors Associated with Severe Hyperbilirubinemia in Term Neonates Admitted for Phototherapy.
Hyperbilirubinemia, Neonatal
Genetic factors in neonatal hyperbilirubinemia and kernicterus.
Hyperbilirubinemia, Neonatal
Genetic polymorphisms in Thai neonates with hyperbilirubinemia.
Hyperbilirubinemia, Neonatal
Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia.
Hyperbilirubinemia, Neonatal
Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn.
Hyperbilirubinemia, Neonatal
Glucose induces intestinal human UDP-glucuronosyltransferase (UGT) 1A1 to prevent neonatal hyperbilirubinemia.
Hyperbilirubinemia, Neonatal
Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia.
Hyperbilirubinemia, Neonatal
Gly71Arg mutation of the bilirubin UDP-glucuronosyltransferase 1A1 gene is associated with neonatal hyperbilirubinemia in the Japanese population.
Hyperbilirubinemia, Neonatal
Heme oxygenase-1 gene variants and hyperbilirubinemia risk in North Indian newborns.
Hyperbilirubinemia, Neonatal
Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia.
Hyperbilirubinemia, Neonatal
Humanized UGT1 Mice, Regulation of UGT1A1, and the Role of the Intestinal Tract in Neonatal Hyperbilirubinemia and Breast Milk-Induced Jaundice.
Hyperbilirubinemia, Neonatal
Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study.
Hyperbilirubinemia, Neonatal
Impact of fatty acids on human UDP-glucuronosyltransferase 1A1 activity and its expression in neonatal hyperbilirubinemia.
Hyperbilirubinemia, Neonatal
Importance of UDP-Glucuronosyltransferase 1A1 Expression in Skin and Its Induction by UVB in Neonatal Hyperbilirubinemia.
Hyperbilirubinemia, Neonatal
Intestinal NCoR1, a regulator of epithelial cell maturation, controls neonatal hyperbilirubinemia.
Hyperbilirubinemia, Neonatal
Investigating Whether Screening or Testing for the Variation Status of UGT 1A1 Gene is Helpful in Managing Neonatal Hyperbilirubinemia.
Hyperbilirubinemia, Neonatal
Molecular genetics of unconjugated hyperbilirubinemia in Taiwanese.
Hyperbilirubinemia, Neonatal
Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese.
Hyperbilirubinemia, Neonatal
Neonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients.
Hyperbilirubinemia, Neonatal
Neonatal hyperbilirubinemia and Gly71Arg mutation of UGT1A1 gene: a Chinese case-control study followed by systematic review of existing evidence.
Hyperbilirubinemia, Neonatal
Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese.
Hyperbilirubinemia, Neonatal
Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene: the common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese.
Hyperbilirubinemia, Neonatal
Neonatal hyperbilirubinemia in Japanese neonates: analysis of the heme oxygenase-1 gene and fetal hemoglobin composition in cord blood.
Hyperbilirubinemia, Neonatal
Obstetric Obesity is Associated with Neonatal Hyperbilirubinemia with High Prevalence in Native Hawaiians and Pacific Island Women.
Hyperbilirubinemia, Neonatal
Prevalence of uridine glucuronosyl transferase 1A1 (UGT1A1) mutations in Malay neonates with severe jaundice.
Hyperbilirubinemia, Neonatal
Profiling of UGT1A1*6, UGT1A1*60, UGT1A1*93, and UGT1A1*28 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR Sequencing.
Hyperbilirubinemia, Neonatal
Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate- glucuronosyltransferase gene.
Hyperbilirubinemia, Neonatal
Relationship between bilirubin UDP-glucuronosyl transferase 1A1 gene and neonatal hyperbilirubinemia.
Hyperbilirubinemia, Neonatal
Risk assessment of gene variants for neonatal hyperbilirubinemia in Taiwan.
Hyperbilirubinemia, Neonatal
Role of extrahepatic UDP-glucuronosyltransferase 1A1: Advances in understanding breast milk-induced neonatal hyperbilirubinemia.
Hyperbilirubinemia, Neonatal
Roles of UGT1A1 Gly71Arg and TATA promoter polymorphisms in neonatal hyperbilirubinemia: A meta-analysis.
Hyperbilirubinemia, Neonatal
Screening for G71R mutation of the UDP-glucuronosyltransferase 1 (UGT1A1) gene in neonates with pathologic and prolonged hyperbilirubinemia in Turkey.
Hyperbilirubinemia, Neonatal
Severe Neonatal Hyperbilirubinemia and UGT1A1 Promoter Polymorphism.
Hyperbilirubinemia, Neonatal
SLCO1B1 c.388A?>?G variant incidence and the severity of hyperbilirubinemia in Indonesian neonates.
Hyperbilirubinemia, Neonatal
The relationship between hyperbilirubinemia and the promoter region and first exon of UGT1A1 gene polymorphisms in Vietnamese newborns.
Hyperbilirubinemia, Neonatal
The role of UGT1A1 (c.-3279?T?>?G) gene polymorphisms in neonatal hyperbilirubinemia susceptibility.
Hyperbilirubinemia, Neonatal
UGT1A1 gene and neonatal hyperbilirubinemia: a preliminary study from Bengkulu, Indonesia.
Hyperbilirubinemia, Neonatal
UGT1A1 gene mutations and neonatal hyperbilirubinemia in Guangxi Heiyi Zhuang and Han populations.
Hyperbilirubinemia, Neonatal
UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China.
Hyperbilirubinemia, Neonatal
UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms versus neonatal hyperbilirubinemia: is there an association?
Hyperbilirubinemia, Neonatal
[Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert syndrome]
Hyperbilirubinemia, Neonatal
[Prolonged neonatal hyperbilirubinemia associated with a UGT1A1 gene mutation]
Hyperbilirubinemia, Neonatal
[Role of genetic factors in occurrence of neonatal jaundice in Guangxi region]
Hyperbilirubinemia, Neonatal
[Roles of UGT 1A1 gene mutation in the development of neonatal hyperbilirubinemia in Guangxi].
Hypercholesterolemia
Enhancement of hepatic drug biotransformation rate by polychlorinated biphenyls in rats fed cholesterol-rich diet.
Hyperglycemia
Tumor-targeted delivery of 8-hydroxyquinoline.
Hyperprolactinemia
UGT1A1 polymorphisms associated with prolactin response in risperidone-treated children and adolescents with autism spectrum disorder.
Hypersensitivity
Application of a pharmacogenetic test adoption model to six oncology biomarkers.
Hypersensitivity
Pharmacogenetics of antiretrovirals.
Hypertension
''Iatrogenic Gilbert syndrome''- A strategy for reducing vascular and cancer risk by increasing plasma unconjugated bilirubin.
Hypertension
A UGT1A1 variant is associated with serum total bilirubin levels, which are causal for hypertension in African-ancestry individuals.
Hypertension
Effects of UGT1A1 Polymorphism, Gender and Triglyceride on the Pharmacokinetics of Telmisartan in Chinese Patients with Hypertension: A Population Pharmacokinetic Analysis.
Hyperthyroidism
Thyroid hormones and the hepatic handling of bilirubin. II. Effects of hypothyroidism and hyperthyroidism on the apparent maximal biliary secretion of bilirubin in the Wistar rat.
Hypogonadism
UGT2B17 Genotype and the Pharmacokinetic Serum Profile of Testosterone during Substitution Therapy with Testosterone Undecanoate. A Retrospective Experience from 207 Men with Hypogonadism.
Hypothyroidism
Thyroid hormones and the hepatic handling of bilirubin. I. Effects of hypothyroidism and hyperthyroidism on the hepatic transport of bilirubin mono- and diconjugates in the Wistar rat.
Hypothyroidism
[Analysis of genes related to hypothyroidism during pregnancy].
Infections
Antihepatotoxic properties of uridine-diphosphoglucose in liver fluke infection. Experimental fascioliasis in the rat.
Infections
Characterization of autoantibodies against uridine-diphosphate glucuronosyltransferase in patients with inflammatory liver diseases.
Infections
Correlations between polymorphisms in the uridine diphosphate-glucuronosyltransferase 1A and C-C motif chemokine receptor 5 genes and infection with the hepatitis B virus in three ethnic groups in China.
Infections
Effect of Traumatic Brain Injury, Erythropoietin, and Anakinra on Hepatic Metabolizing Enzymes and Transporters in an Experimental Rat Model.
Infections
Efficacy of glutathione for treatment of fascioliasis. An investigation in the experimentally infested rat.
Infections
Expression and characterization of recombinant human UDP-glucuronosyltransferases (UGTs). UGT1A9 is more resistant to detergent inhibition than other UGTs and was purified as an active dimeric enzyme.
Infections
EXPRESSION OF UDP-GLUCURONOSYLTRANSFERASE ISOFORM mRNAS DURING INFLAMMATION AND INFECTION IN MOUSE LIVER AND KIDNEY.
Infections
Infection (Actinobacillus pleuropneumoniae)-mediated suppression of oxidative hepatic drug metabolism and cytochrome P4503A mRNA levels in pigs.
Infections
Influence of SLCO1B1 521T>C, UGT2B7 802C>T and IMPDH1 -106G>A Genetic Polymorphisms on Mycophenolic Acid Levels and Adverse Reactions in Chinese Autoimmune Disease Patients.
Infections
Influence of UDP-glucuronosyltransferase polymorphisms on mycophenolate mofetil-induced side effects in kidney transplant patients.
Infections
Risk factors for severe hyperbilirubinemia in neonates.
Infections
Single-nucleotide polymorphisms in the UDP-glucuronosyltransferase 1A-3' untranslated region are associated with atazanavir-induced nephrolithiasis in patients with HIV-1 infection: a pharmacogenetic study.
Infections
Testosterone response of hepatic gene expression in female mice having acquired testosterone-unresponsive immunity to Plasmodium chabaudi malaria.
Infections
The effect of malaria infection on 3'-azido-3'-deoxythymidine and paracetamol glucuronidation in rat liver microsomes.
Infections
The effects of fascioliasis on the activities of some drug-metabolizing enzymes in desert sheep liver.
Infections
UDP-glucuronosyltransferase 1A7 genetic polymorphisms are associated with hepatocellular carcinoma in japanese patients with hepatitis C virus infection.
Infections
UDP-glucuronosyltransferase 1A7 genetic polymorphisms are associated with hepatocellular carcinoma risk and onset age.
Infections
UDP-glucuronosyltransferase 1A7 polymorphisms are associated with liver cirrhosis.
Infertility
A diet containing the soy phytoestrogen genistein causes infertility in female rats partially deficient in UDP glucuronyltransferase.
Inflammatory Bowel Diseases
Crohn's disease in Japanese is associated with a SNP-haplotype of N-acetyltransferase 2 gene.
Inflammatory Bowel Diseases
Genetic variants of UDP-glucuronosyltransferase 1A genes are associated with disease presentation and outcome in primary sclerosing cholangitis.
Insulin Resistance
The uridine diphosphate glucuronosyltransferase 2B15 D85Y and 2B17 deletion polymorphisms predict the glucuronidation pattern of androgens and fat mass in men.
Intermittent Claudication
Association between the UGT1A1 TA-repeat polymorphism and bilirubin concentration in patients with intermittent claudication: results from the CAVASIC study.
Intestinal Neoplasms
Deficient UDP-glucuronosyltransferase detoxification enzyme activity in the small intestinal mucosa of patients with coeliac disease.
Iron Overload
Coexistence of HFE and rare UGT1A1 genes mutations in patients with iron overload related liver injury.
Iron Overload
UGT1A1 gene polymorphism as a potential factor inducing iron overload in the pathogenesis of type 1 hereditary hemochromatosis.
Jaundice, Chronic Idiopathic
Biochemical and molecular aspects of genetic disorders of bilirubin metabolism.
Jaundice, Neonatal
A polymorphic mutation, c.-3279T>G, in the UGT1A1 promoter is a risk factor for neonatal jaundice in the Malay population.
Jaundice, Neonatal
A variant TATA box in the bilirubin UDP-glucuronosyltransferase 1 gene promoter does not contribute to neonatal jaundice in the Japanese population.
Jaundice, Neonatal
Gene Mutation in Neonatal Jaundice - Mutations in UGT1A1 and OATP2 Genes.
Jaundice, Neonatal
Genetic Analysis of UGT1A1 Polymorphisms Using Preserved Dried Umbilical Cord for Assessing the Potential of Neonatal Jaundice as a Risk Factor for Autism Spectrum Disorder in Children.
Jaundice, Neonatal
Gilbert syndrome accelerates development of neonatal jaundice.
Jaundice, Neonatal
Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn.
Jaundice, Neonatal
Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese.
Jaundice, Neonatal
Neonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients.
Jaundice, Neonatal
Polymorphic Variants of UGT1A1 in Neonatal Jaundice in Southern Brazil.
Jaundice, Neonatal
Prevalence of UGT1A1 (TA)n promoter polymorphism in Panamanians neonates with G6PD deficiency.
Jaundice, Neonatal
Prevalence of uridine glucuronosyl transferase 1A1 (UGT1A1) mutations in Malay neonates with severe jaundice.
Jaundice, Neonatal
Screening for G71R mutation of the UGT1A1 gene in the Javanese-Indonesian and Malay-Malaysian populations.
Jaundice, Neonatal
The frequency of UDP-glucuronosyltransferase 1A1 promoter region (TA)7 polymorphism in newborns and it's relation with jaundice.
Jaundice, Neonatal
The relationship between hyperbilirubinemia and the promoter region and first exon of UGT1A1 gene polymorphisms in Vietnamese newborns.
Jaundice, Neonatal
The role of UGT1A1 promoter polymorphism and exon-1 mutations in neonatal jaundice.
Jaundice, Neonatal
[Interest in the study of genetic variants of the promoter region of the UGT1A1 gene in neonatal jaundice]
Jaundice, Neonatal
[UDP-glucuronosyltransferase 1A1 gene and neonatal jaundice]
Kernicterus
A difference in mortality between two strains of jaundiced rats.
Kernicterus
Bilirubin glucuronidation revisited: proper assay conditions to estimate enzyme kinetics with recombinant UGT1A1.
Kernicterus
Gene Replacement Therapy for Genetic Hepatocellular Jaundice.
Kernicterus
Genetic factors in neonatal hyperbilirubinemia and kernicterus.
Kernicterus
Humanized UGT1 Mice, Regulation of UGT1A1, and the Role of the Intestinal Tract in Neonatal Hyperbilirubinemia and Breast Milk-Induced Jaundice.
Kernicterus
Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia and may lead to neonatal kernicterus.
Kernicterus
Intestinal NCoR1, a regulator of epithelial cell maturation, controls neonatal hyperbilirubinemia.
Kernicterus
Kernicterus Associated with Hereditary Spherocytosis and UGT1A1 Promoter Polymorphism.
Kernicterus
Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism?
Kernicterus
Removal of protein-bound and unbound unconjugated bilirubin by perfusion of plasma through an anion-exchange resin in a case of Crigler-Najjar syndrome type I.
Kernicterus
Retrovirus-mediated expression of HUG Br1 in Crigler-Najjar syndrome type I human fibroblasts and correction of the genetic defect in Gunn rat hepatocytes.
Kernicterus
[Advances in research on regulatory effects of chemical ingredients of traditional Chinese medicine on UDP-glucuronosyltransferase 1A1 expression and activity].
Kidney Diseases
Dolutegravir in Mexico for special populations: A cost analysis perspective.
Kidney Failure, Chronic
Concurrence of UGT1A polymorphism and end-stage renal disease leads to severe toxicities of irinotecan in a patient with metastatic colon cancer.
Kidney Neoplasms
Expression of UGT2B7 is driven by two mutually exclusive promoters and alternative splicing in human tissues: changes from prenatal life to adulthood and in kidney cancer.
Kidney Neoplasms
The Intratumoral Balance between Metabolic and Immunologic Gene Expression Is Associated with Anti-PD-1 Response in Patients with Renal Cell Carcinoma.
Laryngeal Neoplasms
Association between UGT1A1 Polymorphism and Risk of Laryngeal Squamous Cell Carcinoma.
Laryngeal Neoplasms
Combined effect of genetic polymorphisms in phase I and II biotransformation enzymes on head and neck cancer risk.
Laryngeal Neoplasms
Genetic polymorphism in the conjugating enzyme UGT1A1 and the risk of head and neck cancer.
Laryngeal Neoplasms
Genetic polymorphisms in the tobacco smoke carcinogens detoxifying enzyme UGT1A7 and the risk of head and neck cancer.
Leprosy
Influence of Genetic Ancestry on INDEL Markers of NFK?1, CASP8, PAR1, IL4 and CYP19A1 Genes in Leprosy Patients.
Leukemia
Contribution of UGT1A1 variations to chemotherapy-induced unconjugated hyperbilirubinemia in pediatric leukemia patients.
Leukemia
GLI1-Inducible Glucuronidation Targets a Broad Spectrum of Drugs.
Leukemia
Principal drug-metabolizing enzyme systems in L1210 leukemia sensitive or resistant to BCNU in vivo.
Leukemia, Lymphocytic, Chronic, B-Cell
Inactivation of Prostaglandin E2 as a Mechanism for UGT2B17-Mediated Adverse Effects in Chronic Lymphocytic Leukemia.
Leukemia, Lymphocytic, Chronic, B-Cell
Overexpression of uridine diphospho glucuronosyltransferase 2B17 in high-risk chronic lymphocytic leukemia.
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Association between severe toxicity of nilotinib and UGT1A1 polymorphisms in Japanese patients with chronic myelogenous leukemia.
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Influence of UGT1A1 *6, *27, and *28 polymorphisms on nilotinib-induced hyperbilirubinemia in Japanese patients with chronic myeloid leukemia.
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Tyrosine kinase inhibitor resistance: a case report on chronic myeloid leukemia and Gilbert's syndrome.
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
UGT1A1 genotype does not affect tyrosine kinase inhibitors efficacy and safety in chronic myeloid leukemia.
Leukemia, Myeloid, Acute
Influence of UGT1A1 polymorphisms on the outcome of acute myeloid leukemia patients treated with cytarabine-base regimens.
Leukemia, Myeloid, Acute
UGT1A1 genotype influences clinical outcome in patients with intermediate-risk acute myeloid leukemia treated with cytarabine-based chemotherapy.
Leukopenia
A prospective study of XELIRI plus bevacizumab as a first-line therapy in Japanese patients with unresectable or recurrent colorectal cancer (KSCC1101).
Leukopenia
Genetic polymorphisms of the UDP-glucuronosyltransferase 1A7 gene and irinotecan toxicity in Japanese cancer patients.
Leukopenia
Glucuronidation of 7-ethyl-10-hydroxycamptothecin (SN-38), an active metabolite of irinotecan (CPT-11), by human UGT1A1 variants, G71R, P229Q, and Y486D.
Leukopenia
Impact of UGT1A1 genetic polymorphism on toxicity in unresectable pancreatic cancer patients undergoing FOLFIRINOX.
Leukopenia
Mycophenolate mofetil-related leukopenia in children and young adults following kidney transplantation: Influence of genes and drugs.
Leukopenia
Phase II study of a triplet regimen of S-1 combined with irinotecan and oxaliplatin in patients with metastatic gastric cancer: clinical and pharmacogenetic results.
Leukopenia
The coffee ingredients caffeic acid and caffeic acid phenylethyl ester protect against irinotecan-induced leukopenia and oxidative stress response.
Leukopenia
UGT genotype may contribute to adverse events following medication with mycophenolate mofetil in pediatric kidney transplant recipients.
Leukopenia
Uridine Glucuronosyltransferase 2B7 Polymorphism-Based Pharmacogenetic Dosing of Epirubicin in FEC Chemotherapy for Early-Stage Breast Cancer.
Leukopenia
[Association of UGT1A1 (*28, *60 and * 93) polymorphism with the adverse reactions of irinotecan chemotherapy in extensive stage small cell lung cancer].
Liver Cirrhosis
Abundance of Phase 1 and 2 Drug-Metabolizing Enzymes in Alcoholic and Hepatitis C Cirrhotic Livers: A Quantitative Targeted Proteomics Study.
Liver Cirrhosis
Dysregulation of UDP-glucuronosyltransferases in CCl4 induced liver injury rats.
Liver Cirrhosis
Hepatic and extrahepatic glucuronidation of bile acids in man. Characterization of bile acid uridine 5'-diphosphate-glucuronosyltransferase in hepatic, renal, and intestinal microsomes.
Liver Cirrhosis
Regulation of uridine diphosphate-glucuronosyltransferase 1A expression by miRNA-214-5p and miRNA-486-3p.
Liver Cirrhosis
UDP-glucuronosyltransferase 1A7 polymorphisms are associated with liver cirrhosis.
Liver Cirrhosis
[Regulation of mRNA expression of human UDP-glucuronosyltransferase in hepatitis and liver cirrhosis patients]
Liver Cirrhosis, Alcoholic
Abundance of Phase 1 and 2 Drug-Metabolizing Enzymes in Alcoholic and Hepatitis C Cirrhotic Livers: A Quantitative Targeted Proteomics Study.
Liver Cirrhosis, Biliary
Characterization of autoantibodies against uridine-diphosphate glucuronosyltransferase in patients with inflammatory liver diseases.
Liver Diseases
Acetaminophen pharmacokinetics in children with nonalcoholic fatty liver disease.
Liver Diseases
Alteration of UDP-glucuronosyltransferase 1a1, 1a7 and P-glycoprotein expression in hepatic fibrosis rats and the impact on pharmacokinetics of puerarin.
Liver Diseases
Altered UDP-glucuronosyltransferase and sulfotransferase expression and function during progressive stages of human nonalcoholic fatty liver disease.
Liver Diseases
Carlinoside reduces hepatic bilirubin accumulation by stimulating bilirubin-UGT activity through Nrf2 gene expression.
Liver Diseases
Characterization of autoantibodies against uridine-diphosphate glucuronosyltransferase in patients with inflammatory liver diseases.
Liver Diseases
Effect of oral administration of ursodeoxycholic acid on rat hepatic and intestinal UDP-glucuronosyltransferase.
Liver Diseases
Function and regulation of UDP-glucuronosyltransferase genes in health and liver disease: report of the Seventh International Workshop on Glucuronidation, September 1993, Pitlochry, Scotland.
Liver Diseases
Genetic link of hepatocellular carcinoma with polymorphisms of the UDP-glucuronosyltransferase UGT1A7 gene.
Liver Diseases
Glucuronidation of hyodeoxycholic acid in human liver. Evidence for a selective role of UDP-glucuronosyltransferase 2B4.
Liver Diseases
Hepatic and extrahepatic glucuronidation of bile acids in man. Characterization of bile acid uridine 5'-diphosphate-glucuronosyltransferase in hepatic, renal, and intestinal microsomes.
Liver Diseases
Hepatic bilirubin UDP-glucuronyltransferase in patients with sickle cell anemia.
Liver Diseases
PLX038: a PEGylated prodrug of SN-38 independent of UGT1A1 activity.
Liver Diseases
Role of UDP-Glucuronosyltransferase 1A1 in the Metabolism and Pharmacokinetics of Silymarin Flavonolignans in Patients with HCV and NAFLD.
Liver Diseases
The frequency, clinical course, and health related quality of life in adults with Gilbert's syndrome: a longitudinal study.
Liver Diseases
UDP glucuronosyltransferase mRNA levels in human liver disease.
Liver Diseases
UDP-glucuronosyltransferase polymorphisms affect diethylnitrosamine-induced carcinogenesis in humanized transgenic mice.
Liver Diseases
UDP-glucuronyltransferase-catalyzed deconjugation of bilirubin monoglucuronide.
Liver Diseases
UGT1A1 polymorphism and hyperbilirubinemia in a patient who received sorafenib.
Liver Diseases
Variants in the UGT1A1 gene and the risk of pediatric nonalcoholic fatty liver disease.
Liver Diseases
[Glucuronyltransferase in chronic liver diseases]
Liver Failure
Association between liver failure and hepatic UDP-glucuronosyltransferase activity in dairy cows with follicular cysts.
Liver Failure, Acute
Acute liver failure enhances oral plasma exposure of zidovudine in rats by downregulation of hepatic UGT2B7 and intestinal P-gp.
Liver Failure, Acute
Genetic polymorphisms in the UDP-glucuronosyltransferase UGT1A7 gene in patients with acute liver failure after kava-kava consumption.
Liver Failure, Acute
Response to Aghdassi et al., Letter to the editor "Genetic polymorphisms in the UDP-glucuronosyltransferase UGT1A7 gene in patients with acute liver failure after kava-kava consumption".
Liver Failure, Acute
The UDP-glucuronosyltransferase (UGT) 1A polymorphism c.2042C>G (rs8330) is associated with increased human liver acetaminophen glucuronidation, increased UGT1A exon 5a/5b splice variant mRNA ratio, and decreased risk of unintentional acetaminophen-induced acute liver failure.
Liver Neoplasms
Epirubicin Upregulates UDP Glucuronosyltransferase 2B7 Expression in Liver Cancer Cells Via the p53 Pathway.
Liver Neoplasms
Genetic link of hepatocellular carcinoma with polymorphisms of the UDP-glucuronosyltransferase UGT1A7 gene.
Liver Neoplasms
Glucuronidation by UGT1A1 is the dominant pathway of the metabolic disposition of belinostat in liver cancer patients.
Liver Neoplasms
Induction of Human UDP-glucuronosyltransferase 2B7 Gene Expression by Cytotoxic Anticancer Drugs in Liver Cancer HepG2 Cells.
Liver Neoplasms
Regulation of UDP-Glucuronosyltransferases UGT2B4 and UGT2B7 by MicroRNAs in Liver Cancer Cells.
Liver Neoplasms
UDP-glucuronosyltransferase polymorphisms affect diethylnitrosamine-induced carcinogenesis in humanized transgenic mice.
Liver Neoplasms
UGT1A7 polymorphisms, polycyclic aromatic hydrocarbons and the development of hepatocellular cancer.
Lung Diseases
Identification of lung adenocarcinoma-specific exosome RNAs in peripheral blood by RNA-Seq analysis.
Lung Neoplasms
Association between the low-dose irinotecan regimen-induced occurrence of grade 4 neutropenia and genetic variants of UGT1A1 in patients with gynecological cancers.
Lung Neoplasms
Association between UGT1A1*28*28 genotype and lung cancer in the Japanese population.
Lung Neoplasms
Association of nephrotoxicity during platinum-etoposide doublet therapy with UGT1A1 polymorphisms in small cell lung cancer patients.
Lung Neoplasms
Carcinogen metabolism and DNA adducts in human lung tissues as affected by tobacco smoking or metabolic phenotype: a case-control study on lung cancer patients.
Lung Neoplasms
Cisplatin combined with irinotecan or etoposide for untreated extensive-stage small cell lung cancer: A multicenter randomized controlled clinical trial.
Lung Neoplasms
Comprehensive analysis of UGT1A polymorphisms predictive for pharmacokinetics and treatment outcome in patients with non-small-cell lung cancer treated with irinotecan and cisplatin.
Lung Neoplasms
Correlations of UGT1A1 gene polymorphisms with onset and prognosis of non-small cell lung cancer.
Lung Neoplasms
Implementation of modern therapy approaches and research for non-small cell lung cancer in Japan.
Lung Neoplasms
Influence of UGT1A1 polymorphism on etoposide plus platinum-induced neutropenia in Japanese patients with small-cell lung cancer.
Lung Neoplasms
Pharmacogenetics in pancreatic cancer. Highlights from the 45th ASCO annual meeting. Orlando, FL, USA. May 29-June 2, 2009.
Lung Neoplasms
Phase I study of irinotecan for previously treated lung cancer patients with the UGT1A1*28 or *6 polymorphism: Results of the Lung Oncology Group in Kyushu (LOGIK1004A).
Lung Neoplasms
Phase I/II pharmacokinetic and pharmacogenomic study of UGT1A1 polymorphism in elderly patients with advanced non-small cell lung cancer treated with irinotecan.
Lung Neoplasms
Polymorphism of UDP-glucuronosyltransferase 1A7 gene: a possible new risk factor for lung cancer.
Lung Neoplasms
Potentially functional genetic variants in PLIN2, SULT2A1 and UGT1A9 genes of the ketone pathway and survival of nonsmall cell lung cancer.
Lung Neoplasms
Pulmonary expression of CYP2A13 and ABCB1 is regulated by FOXA2 and their genetic interaction is associated with lung cancer.
Lung Neoplasms
Study on the Optimal Dose of Irinotecan for Patients with Heterozygous Uridine Diphosphate-Glucuronosyltransferase 1A1 (UGT1A1).
Lung Neoplasms
The relationship between UGT1A1 gene polymorphism and irinotecan effect on extensive-stage small-cell lung cancer.
Lung Neoplasms
The UDP-glucuronosyltransferase 2B17 gene deletion polymorphism: sex-specific association with urinary 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol glucuronidation phenotype and risk for lung cancer.
Lung Neoplasms
UDP-glucuronosyltransferase 2B17 genotype and the risk of lung cancer among Austrian Caucasians.
Lung Neoplasms
UGT1A1 Gene Polymorphisms in Patients with Small Cell Lung Cancer Treated with Irinotecan-Platinum Doublet Chemotherapy and Their Association with Gastrointestinal Toxicity and Overall Survival.
Lung Neoplasms
UGT1A1 polymorphisms with irinotecan-induced toxicities and treatment outcome in Asians with Lung Cancer: a meta-analysis.
Lung Neoplasms
UGT1A10 is responsible for SN-38 glucuronidation and its expression in human lung cancers.
Lung Neoplasms
UGT1A6 Polymorphisms Modulated Lung Cancer Risk in a Chinese Population.
Lung Neoplasms
Weekly regimen of irinotecan/docetaxel in previously treated non-small cell lung cancer patients and correlation with uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) polymorphism.
Lung Neoplasms
[Association of UGT1A1 (*28, *60 and * 93) polymorphism with the adverse reactions of irinotecan chemotherapy in extensive stage small cell lung cancer].
Lung Neoplasms
[Correlation of polymorphisms of UDP-glucuronosyltransferase 1A7 gene to genetic susceptibility of lung cancer]
Lymphatic Metastasis
Differential Expression of the Androgen-Conjugating UGT2B15 and UGT2B17 Enzymes in Prostate Tumor Cells during Cancer Progression.
Lymphoma
Implementation of modern therapy approaches and research for non-small cell lung cancer in Japan.
Lymphoma
Pharmacogenetic study in Hodgkin's lymphomas reveals the impact of UGT1A1 polymorphisms on patient's prognosis.
Lymphoma
UGT1A1 *6 polymorphism predicts outcome in elderly patients with relapsed or refractory diffuse large B-cell lymphoma treated with carboplatin, dexamethasone, etoposide and irinotecan.
Lymphoma, B-Cell
UGT1A1 *6 polymorphism predicts outcome in elderly patients with relapsed or refractory diffuse large B-cell lymphoma treated with carboplatin, dexamethasone, etoposide and irinotecan.
Lymphoma, Large B-Cell, Diffuse
UGT1A1 *6 polymorphism predicts outcome in elderly patients with relapsed or refractory diffuse large B-cell lymphoma treated with carboplatin, dexamethasone, etoposide and irinotecan.
Lymphoma, T-Cell, Peripheral
UGT genotyping in belinostat dosing.
Malaria
Preliminary investigation of the contribution of CYP2A6, CYP2B6, and UGT1A9 polymorphisms on artesunate-mefloquine treatment response in Burmese patients with Plasmodium falciparum malaria.
Malaria
The effect of malaria infection on 3'-azido-3'-deoxythymidine and paracetamol glucuronidation in rat liver microsomes.
Malaria, Falciparum
Preliminary investigation of the contribution of CYP2A6, CYP2B6, and UGT1A9 polymorphisms on artesunate-mefloquine treatment response in Burmese patients with Plasmodium falciparum malaria.
Malnutrition
Differences in response of glucuronide and glutathione conjugating enzymes to aflatoxin B1 and N-acetylaminofluorene in underfed rats.
Massive Hepatic Necrosis
Increase of UDP-glucuronosyltransferase activities toward xenobiotics during the development of hereditary hepatitis in LEC rats.
Mastocytoma
Biosynthesis of heparin. Solubilization and partial purification of uridine diphosphate glucuronic acid: acceptor glucuronosyltransferase from mouse mastocytoma.
Melanoma
Anti-cancer drugs elicit re-expression of UDP-glucuronosyltransferases in melanoma cells.
Melanoma
Detection of Total UDP-Glucuronosyltransferase (UGT) Activity in Melanoma Cells.
Melanosis
Histopathology of melanosis coli and determination of its associated genes by comparative analysis of expression microarrays.
Metabolic Diseases
A translationally optimized AAV-UGT1A1 vector drives safe and long-lasting correction of Crigler-Najjar syndrome.
Metabolic Diseases
Paternal isodisomy for chromosome 2 as the cause of Crigler-Najjar type I syndrome.
Metabolic Syndrome
Disruption of the ugt1 locus in mice resembles human crigler-najjar type I disease.
Metabolic Syndrome
Preparation of reference material for UGT1A1 (TA)n polymorphism genotyping.
Mouth Neoplasms
Genomic profile of oral squamous cell carcinomas with an adjacent leukoplakia or with an erythroleukoplakia that evolved after the treatment of primary tumor: A report of two cases.
Mucocutaneous Lymph Node Syndrome
Polymorphisms of heme oxygenase-1 and bilirubin UDP-glucuronosyltransferase genes are not associated with Kawasaki disease susceptibility.
Muscular Diseases
Statin Lactonization by Uridine 5'-Diphospho-glucuronosyltransferases (UGTs).
Myocardial Ischemia
''Iatrogenic Gilbert syndrome''- A strategy for reducing vascular and cancer risk by increasing plasma unconjugated bilirubin.
Neoplasm Metastasis
Ages of hepatocellular carcinoma occurrence and life expectancy are associated with a UGT2B28 genomic variation.
Neoplasm Metastasis
Alternative promoters control UGT2B17-dependent androgen catabolism in prostate cancer and its influence on progression.
Neoplasm Metastasis
Bioinformatics Analysis to Reveal Potential Differentially Expressed Long Non-Coding RNAs and Genes Associated with Tumour Metastasis in Lung Adenocarcinoma.
Neoplasm Metastasis
Differential Expression of the Androgen-Conjugating UGT2B15 and UGT2B17 Enzymes in Prostate Tumor Cells during Cancer Progression.
Neoplasm Metastasis
High Resectability Rate of Initially Unresectable Colorectal Liver Metastases After UGT1A1-Adapted High-Dose Irinotecan Combined with LV5FU2 and Cetuximab: A Multicenter Phase II Study (ERBIFORT).
Neoplasm Metastasis
Link between colorectal cancer and polymorphisms in the uridine-diphosphoglucuronosyltransferase 1A7 and 1A1 genes.
Neoplasm Metastasis
Maintenance of intratumoral androgens in metastatic prostate cancer: a mechanism for castration-resistant tumor growth.
Neoplasm Metastasis
Molecular genetics of unconjugated hyperbilirubinemia in Taiwanese.
Neoplasm Metastasis
Pilot Study Comparing Systemic and Tissue Pharmacokinetics of Irinotecan and Metabolites after Hepatic Drug-Eluting Chemoembolization.
Neoplasm Metastasis
UDP-glucuronosyltransferases and biochemical recurrence in prostate cancer progression.
Neoplasm Metastasis
UGT2B17 Expedites Progression of Castration-Resistant Prostate Cancers by Promoting Ligand-Independent AR Signaling.
Neoplasm Metastasis
[A Case of Early Anal Canal Cancer with Pagetoid Spread with Different Antitumor Effects of Chemotherapy on Different Metastatic Sites].
Neoplasm Metastasis
[A Case of Unresectable Advanced Rectal Cancer with a Pancreatic Tumor That Was Successfully Treated with FOLFIRINOX].
Neoplasms
1H, 13C and 15N chemical shift assignments of the C-terminal domain of human UDP-Glucuronosyltransferase 2B7 (UGT2B7-C).
Neoplasms
A mode of action for induction of thyroid gland tumors by Pyrethrins in the rat.
Neoplasms
A novel functional polymorphism in the uridine diphosphate-glucuronosyltransferase 2B7 promoter with significant impact on promoter activity.
Neoplasms
A pharmacogenomics study of the human estrogen glucuronosyltransferase UGT1A3.
Neoplasms
A review of gene-drug interactions for nonsteroidal anti-inflammatory drug use in preventing colorectal neoplasia.
Neoplasms
A UGT1A1 genotype-guided dosing study of modified FOLFIRINOX in previously untreated patients with advanced gastrointestinal malignancies.
Neoplasms
A UGT2B17-positive donor is a risk factor for higher transplant-related mortality and lower survival after bone marrow transplantation.
Neoplasms
Activators of the farnesoid X receptor negatively regulate androgen glucuronidation in human prostate cancer LNCAP cells.
Neoplasms
Altered metabolism of polycyclic aromatic hydrocarbons by UDP-glycosyltransferase 3A2 (UGT3A2) missense variants.
Neoplasms
Alternative promoters control UGT2B17-dependent androgen catabolism in prostate cancer and its influence on progression.
Neoplasms
Androgen and estrogen receptors in breast cancer co-regulate human UDP-glucuronosyltransferases 2B15 and 2B17.
Neoplasms
Androgen receptor mediates the expression of UDP-glucuronosyltransferase 2 B15 and B17 genes.
Neoplasms
Androgen receptor signals regulate UDP-glucuronosyltransferases in the urinary bladder: A potential mechanism of androgen-induced bladder carcinogenesis.
Neoplasms
Association between Glucuronidation Genotypes and Urinary NNAL Metabolic Phenotypes in Smokers.
Neoplasms
Association between sex hormones regulation-related SNP rs12233719 and lung cancer risk among never-smoking Chinese women.
Neoplasms
Association between the low-dose irinotecan regimen-induced occurrence of grade 4 neutropenia and genetic variants of UGT1A1 in patients with gynecological cancers.
Neoplasms
Association of carboxylesterase 1A genotypes with irinotecan pharmacokinetics in Japanese cancer patients.
Neoplasms
Association of UGT2B7 and ABCB1 genotypes with morphine-induced adverse drug reactions in Japanese patients with cancer.
Neoplasms
Associations between UGT1A1*6 or UGT1A1*6/*28 polymorphisms and irinotecan-induced neutropenia in Asian cancer patients.
Neoplasms
Associations between UGT2B7 polymorphisms and cancer susceptibility: A meta-analysis.
Neoplasms
Bilirubin UDP-glucuronosyltransferase 1A1 gene polymorphisms: susceptibility to oxidative damage and cancer?
Neoplasms
Bioinformatic analysis suggests that UGT2B15 activates the Hippo?YAP signaling pathway leading to the pathogenesis of gastric cancer.
Neoplasms
Brain-derived neurotrophic factor involved epigenetic repression of UGT2B7 in colorectal carcinoma: A mechanism to alter morphine glucuronidation in tumor.
Neoplasms
Can UGT1A1 genotyping reduce morbidity and mortality in patients with metastatic colorectal cancer treated with irinotecan? An evidence-based review.
Neoplasms
Carcinogen metabolism and DNA adducts in human lung tissues as affected by tobacco smoking or metabolic phenotype: a case-control study on lung cancer patients.
Neoplasms
Characterization of UDP-glucuronosyltransferase (UGT1A1) Promoter Polymorphisms and Gene Expression on Ethnicity, Stage of Disease, and Menopausal Status in Breast Cancer.
Neoplasms
Chondroitin synthases I, II, III and chondroitin sulfate glucuronyltransferase expression in colorectal cancer.
Neoplasms
Chromosomal structural variations during progression of a prostate epithelial cell line to a malignant metastatic state inactivate the NF2, NIPSNAP1, UGT2B17 and LPIN2 genes.
Neoplasms
Cisplatin plus weekly CPT-11/docetaxel in advanced esophagogastric cancer: a phase I study with pharmacogenetic assessment of XPD, XRCC3 and UGT1A1 polymorphisms.
Neoplasms
Clinical significance of UDP-glucuronosyltransferase 1A1*6 for toxicities of combination chemotherapy with irinotecan and cisplatin in gynecologic cancers: a prospective multi-institutional study.
Neoplasms
Comparative patterns of hepatic drug metabolizing enzymes and their possible correlation with chromosomal aberrations in transplantable murine lymphoma: a time course study.
Neoplasms
Comparative untargeted proteomic analysis of ADME proteins and tumor antigens for tumor cell lines.
Neoplasms
Comparison of mouse and human colon tumors with regard to phase I and phase II drug-metabolizing enzyme systems.
Neoplasms
Copy number polymorphisms in new HapMap III and Singapore populations.
Neoplasms
Correlation between the UDP-glucuronosyltransferase (UGT1A1) TATAA box polymorphism and carcinogen detoxification phenotype: significantly decreased glucuronidating activity against benzo(a)pyrene-7,8-dihydrodiol(-) in liver microsomes from subjects with the UGT1A1*28 variant.
Neoplasms
Correlations of UGT1A1 gene polymorphisms with onset and prognosis of non-small cell lung cancer.
Neoplasms
Cross-Talk between Alternatively Spliced UGT1A Isoforms and Colon Cancer Cell Metabolism.
Neoplasms
Detection of UGT1A10 polymorphisms and their association with orolaryngeal carcinoma risk.
Neoplasms
Determination of ancestral allele for possible human cancer-associated polymorphisms.
Neoplasms
Development of a novel, fully-automated genotyping system: principle and applications.
Neoplasms
Differential allelic expression of c.1568C > A at UGT2B15 is due to variation in a novel cis-regulatory element in the 3'UTR.
Neoplasms
Differential down-regulation of the UDP-glucuronosyltransferase 1A locus is an early event in human liver and biliary cancer.
Neoplasms
Differential Expression of the Androgen-Conjugating UGT2B15 and UGT2B17 Enzymes in Prostate Tumor Cells during Cancer Progression.
Neoplasms
Differential expression of the UGT1A family of genes in stomach cancer tissues.
Neoplasms
Direct haplotyping of kilobase-size DNA using carbon nanotube probes.
Neoplasms
Distribution of uridine diphosphate glucuronosyltransferase 1A polymorphisms and their role in irinotecan-induced toxicity in patients with cancer.
Neoplasms
Diversified expression of aryl hydrocarbon receptor dependent genes in human laryngeal squamous cell carcinoma cell lines treated with ?-naphthoflavone.
Neoplasms
Docetaxel and irinotecan in recurrent or metastatic head and neck cancer: a phase 2 trial of the Eastern Cooperative Oncology Group.
Neoplasms
Dose-finding and pharmacokinetic study to optimize the dosing of irinotecan according to the UGT1A1 genotype of patients with cancer.
Neoplasms
DPYD and UGT1A1 pharmacogenetic testing in patients with gastrointestinal malignancies: an overview of the evidence and considerations for clinical implementation.
Neoplasms
DPYD*2A/*5A/*9A and UGT1A1*6/*28 polymorphisms in Chinese colorectal cancer patients.
Neoplasms
Drug-Metabolizing Activity, Protein and Gene Expression of UDP-Glucuronosyltransferases Are Significantly Altered in Hepatocellular Carcinoma Patients.
Neoplasms
Drug-metabolizing enzymes in pharyngeal mucosa and in oropharyngeal cancer tissue.
Neoplasms
Effect of dapagliflozin on colon cancer cell [Rapid Communication].
Neoplasms
Effect of orally administered phenethyl isothiocyanate on hepatic gene expression in rats.
Neoplasms
Effect of UGT2B17 deletion polymorphism on prognosis in pediatric cancer.
Neoplasms
Effects of UGT1A1 genotype on the pharmacokinetics, pharmacodynamics, and toxicities of belinostat administered by 48-hour continuous infusion in patients with cancer.
Neoplasms
Emerging roles for UDP-glucuronosyltransferases in drug resistance and cancer progression.
Neoplasms
Enhanced Activity of P4503A4 and UGT1A10 Induced by Acridinone Derivatives C-1305 and C-1311 in MCF-7 and HCT116 Cancer Cells: Consequences for the Drugs' Cytotoxicity, Metabolism and Cellular Response.
Neoplasms
Enhanced hepatic drug clearance in patients with cystic fibrosis.
Neoplasms
Establishment of the experimental procedure for prediction of conjugation capacity in mutant UGT1A1.
Neoplasms
Evaluation of the Association of Perioperative UGT1A1 Genotype-Dosed gFOLFIRINOX With Margin-Negative Resection Rates and Pathologic Response Grades Among Patients With Locally Advanced Gastroesophageal Adenocarcinoma: A Phase 2 Clinical Trial.
Neoplasms
Exemestane and Its Active Metabolite 17-Hydroexemestane Induce UDP-Glucuronosyltransferase (UGT) 2B17 Expression in Breast Cancer Cells.
Neoplasms
Expression of drug-metabolizing enzymes and P-170 glycoprotein in colorectal carcinoma and normal mucosa.
Neoplasms
Expression of glutathione S-transferase and phenol sulfotransferase, but not of UDP-glucuronosyltransferase, in the human lung tumor cell lines NCI-H322 and NCI-H358.
Neoplasms
Expression of UDP Glucuronosyltransferases 2B15 and 2B17 is associated with methylation status in prostate cancer cells.
Neoplasms
Expression of UDP-glucuronosyltransferase 1A in bladder cancer: Association with prognosis and regulation by estrogen.
Neoplasms
Expression of UGT2B7, a UDP-glucuronosyltransferase implicated in the metabolism of 4-hydroxyestrone and all-trans retinoic acid, in normal human breast parenchyma and in invasive and in situ breast cancers.
Neoplasms
Factors Affecting Interindividual Variability of Hepatic UGT2B17 Protein Expression Examined Using a Novel Specific Monoclonal Antibody.
Neoplasms
Functional characterization of human UDP-glucuronosyltransferase 1A9 variant, D256N, found in Japanese cancer patients.
Neoplasms
Genetic link of hepatocellular carcinoma with polymorphisms of the UDP-glucuronosyltransferase UGT1A7 gene.
Neoplasms
Genetic linkage of UGT1A7 and UGT1A9 polymorphisms to UGT1A1*6 is associated with reduced activity for SN-38 in Japanese patients with cancer.
Neoplasms
Genetic polymorphisms in human SULT1A1 and UGT1A1 genes associate with breast tumor characteristics: a case-series study.
Neoplasms
Genetic polymorphisms in human UDP-glucuronosyltransferases 1A7 and the risk of gastrointestinal carcinomas: A systematic review and network meta-analysis.
Neoplasms
Genetic polymorphisms in the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene and prostate cancer risk in Caucasian men.
Neoplasms
Genetic polymorphisms in UDP-glucuronosyltransferase 1A6 and 1A7 and the risk for benign Warthin's tumors of the parotid gland.
Neoplasms
Genetic polymorphisms of human UDP-glucuronosyltransferase (UGT) genes and cancer risk.
Neoplasms
Genetic polymorphisms of the UDP-glucuronosyltransferase 1A7 gene and irinotecan toxicity in Japanese cancer patients.
Neoplasms
Genetic polymorphisms of the uridine diphosphate glucuronosyltransferase 1A7 and colorectal cancer risk in relation to cigarette smoking and alcohol drinking in a Chinese population.
Neoplasms
Genetic polymorphisms of UGT1A7 and cancer risk: evidence from 21 case-control studies.
Neoplasms
Genetic variants in the UDP-glucuronosyltransferase 1A1 gene predict the risk of severe neutropenia of irinotecan.
Neoplasms
Genetic variants in the UGT1A6 enzyme, aspirin use, and the risk of colorectal adenoma.
Neoplasms
Genetic variants of UGT1A6 influence risk of colorectal adenoma recurrence.
Neoplasms
Genetic variations and haplotypes of UGT1A4 in a Japanese population.
Neoplasms
Genomic profile of oral squamous cell carcinomas with an adjacent leukoplakia or with an erythroleukoplakia that evolved after the treatment of primary tumor: A report of two cases.
Neoplasms
Genotype-phenotype correlation between the polymorphic UGT2B17 gene deletion and NNAL glucuronidation activities in human liver microsomes.
Neoplasms
GLI1-Inducible Glucuronidation Targets a Broad Spectrum of Drugs.
Neoplasms
Glucuronidation and the UDP-glucuronosyltransferases in health and disease.
Neoplasms
Glucuronidation of Anticancer Prodrug PR-104A: Species Differences, Identification of Human UDP-glucuronosyltransferases and Implications for Therapy.
Neoplasms
Glucuronidation of SN-38 and NU/ICRF 505 in human colon cancer and adjacent normal colon.
Neoplasms
Glucuronosyltransferase activity in human cancer cell line LNCaP.
Neoplasms
Identification and functional characterization of a novel UGT2A1 splice variant: Potential importance in tobacco-related cancer susceptibility.
Neoplasms
Identification of a prevalent functional missense polymorphism in the UGT2B10 gene and its association with UGT2B10 inactivation against tobacco-specific nitrosamines.
Neoplasms
Identification of low-frequency variants of UGT1A3 associated with bladder cancer risk by next-generation sequencing.
Neoplasms
Imatinib-induced hyperbilirubinemia with UGT1A1 (*28) promoter polymorphism: first case series in patients with gastrointestinal stromal tumor.
Neoplasms
Impact of UDP-gluconoryltransferase 2B17 genotype on vorinostat metabolism and clinical outcomes in Asian women with breast cancer.
Neoplasms
Impact of UGT1A1 genotype upon toxicities of combination with low-dose irinotecan plus platinum.
Neoplasms
Importance of UDP-glucuronosyltransferase 1A1( *)6 for irinotecan toxicities in Japanese cancer patients.
Neoplasms
Importance of UDP-glucuronosyltransferase 1A10 (UGT1A10) in the detoxification of polycyclic aromatic hydrocarbons: decreased glucuronidative activity of the UGT1A10139Lys isoform.
Neoplasms
In vitro characterization of hepatic flavopiridol metabolism using human liver microsomes and recombinant UGT enzymes.
Neoplasms
Increase in thyroid follicular cell tumors in nelfinavir-treated rats observed in a 2-year carcinogenicity study is consistent with a rat-specific mechanism of thyroid neoplasia.
Neoplasms
Increased UDP-glucuronyltransferase and gamma-glutamyltranspeptidase in enzyme-altered rat liver lesions produced by low doses of aflatoxin B1.
Neoplasms
Increased UGT1A3 and UGT1A7 Expression is Associated with Pancreatic Cancer.
Neoplasms
Induction of UDP-glucuronosyltransferase 2B15 gene expression by the major active metabolites of tamoxifen, 4-hydroxytamoxifen and endoxifen, in breast cancer cells.
Neoplasms
Influence of UGT1A1 *6/*28 Polymorphisms on Irinotecan-Related Toxicity and Survival in Pediatric Patients with Relapsed/Refractory Solid Tumors Treated with the VIT Regimen.
Neoplasms
Influence of UGT1A9 intronic I399C>T polymorphism on SN-38 glucuronidation in Asian cancer patients.
Neoplasms
Inhibition of epigallocatechin gallate on orthotopic colon cancer by upregulating the Nrf2-UGT1A signal pathway in nude mice.
Neoplasms
Inhibition of UDP-glucuronosyltransferase by aglycons of natural glucuronides in kampo medicines using SN-38 as a substrate.
Neoplasms
Interaction Between Sex and Organic Anion-Transporting Polypeptide 1b2 on the Pharmacokinetics of Regorafenib and Its Metabolites Regorafenib-N-Oxide and Regorafenib-Glucuronide in Mice.
Neoplasms
Interethnic Variations of UGT1A1 and UGT1A7 Polymorphisms in the Jordanian Population.
Neoplasms
Interpreting disparate responses to cancer therapy: the role of human population genetics.
Neoplasms
Intestinal glucuronidation protects against chemotherapy-induced toxicity by irinotecan (CPT-11).
Neoplasms
Invader UGT1A1 molecular assay for irinotecan toxicity. A genetic test for an increased risk of toxicity from the cancer chemotherapy drug irinotecan (Camptosar).
Neoplasms
Irinotecan inactivation is modulated by epigenetic silencing of UGT1A1 in colon cancer.
Neoplasms
Irinotecan pharmacokinetics/pharmacodynamics and UGT1A genetic polymorphisms in Japanese: roles of UGT1A1*6 and *28.
Neoplasms
Irinotecan treatment in cancer patients with UGT1A1 polymorphisms.
Neoplasms
Is bilirubin a marker of vascular disease and/or cancer and is it a potential therapeutic target?
Neoplasms
Jiawei Xianglian Decoction (JWXLD), a Traditional Chinese Medicine (TCM), Alleviates CPT-11-Induced Diarrhea in Mice.
Neoplasms
Linkage disequilibrium across the UGT1A locus should not be ignored in association studies of cancer susceptibility.
Neoplasms
Loss of exogenous androgen dependence by prostate tumor cells is associated with elevated glucuronidation potential.
Neoplasms
Main drug-metabolizing enzyme systems in human breast tumors and peritumoral tissues.
Neoplasms
Maintenance of intratumoral androgens in metastatic prostate cancer: a mechanism for castration-resistant tumor growth.
Neoplasms
Mechanisms of fat-related modulation of N-nitrosodiethylamine-induced tumors in rats: organ distribution, blood lipids, enzymes and pro-oxidant state.
Neoplasms
Meta-analysis reveals a lack of association between UGT2B17 deletion polymorphism and tumor susceptibility.
Neoplasms
Metabolic Profiles of New Unsymmetrical Bisacridine Antitumor Agents in Electrochemical and Enzymatic Noncellular Systems and in Tumor Cells.
Neoplasms
Metabolic transformation of antitumor acridinone C-1305 but not C-1311 via selective cellular expression of UGT1A10 increases cytotoxic response: implications for clinical use.
Neoplasms
miR-452 Reverses Abnormal Glycosylation Modification of ER? and Estrogen Resistance in TNBC (Triple-Negative Breast Cancer) Through Targeting UGT1A1.
Neoplasms
Modulation of NRF2 and UGT1A expression by epigallocatechin-3-gallate in colon cancer cells and BALB/c mice.
Neoplasms
Modulation of UDP-glucuronidation by acridinone antitumor agents C-1305 and C-1311 in HepG2 and HT29 cell lines, despite slight impact in noncellular systems.
Neoplasms
Morphine glucuronidation in human fetal and adult liver.
Neoplasms
Morphine glucuronide-to-morphine plasma ratios are unaffected by the UGT2B7 H268Y and UGT1A1*28 polymorphisms in cancer patients on chronic morphine therapy.
Neoplasms
Multicenter, Randomized, Phase III Trial of Neoadjuvant Chemoradiation With Capecitabine and Irinotecan Guided by UGT1A1 Status in Patients With Locally Advanced Rectal Cancer.
Neoplasms
North Central Cancer Treatment Group N0543 (Alliance): A phase 2 trial of pharmacogenetic-based dosing of irinotecan, oxaliplatin, and capecitabine as first-line therapy for patients with advanced small bowel adenocarcinoma.
Neoplasms
Novel single nucleotide polymorphism of UGT1A7 gene in Japanese.
Neoplasms
Novel single nucleotide polymorphism of UGT1A9 gene in Japanese.
Neoplasms
Oncologic Outcomes in Metastatic Colorectal Cancer with Regorafenib with FOLFIRI as a Third- or Fourth-Line Setting.
Neoplasms
Overcoming Drug Resistance through the Development of Selective Inhibitors of UDP-Glucuronosyltransferase Enzymes.
Neoplasms
Overexpression of lipid metabolism genes and PBX1 in the contralateral breasts of women with estrogen receptor-negative breast cancer.
Neoplasms
Overexpression of uridine diphospho glucuronosyltransferase 2B17 in high-risk chronic lymphocytic leukemia.
Neoplasms
Patterns of cancer genetic testing: a randomized survey of Oregon clinicians.
Neoplasms
Pharmacogenetic impact of polymorphisms in the coding region of the UGT1A1 gene on SN-38 glucuronidation in Japanese patients with cancer.
Neoplasms
Pharmacogenetic study in gastric cancer patients treated with adjuvant fluorouracil/leucovorin or epirubicin/cisplatin/fluorouracil before and after chemoradiation on CALGB 80101 (Alliance).
Neoplasms
Pharmacogenetics of anticancer agents: lessons from amonafide and irinotecan.
Neoplasms
Pharmacogenetics of irinotecan toxicity.
Neoplasms
Pharmacogenetics of irinotecan: a promoter polymorphism of UGT1A1 gene and severe adverse reactions to irinotecan.
Neoplasms
Pharmacogenomics of colorectal cancer prevention and treatment.
Neoplasms
Pharmacogenomics of tamoxifen and irinotecan therapies.
Neoplasms
Phase II Drug-Metabolizing Polymorphisms and Smoking Predict Recurrence of Non-Muscle-Invasive Bladder Cancer: A Gene-Smoking Interaction.
Neoplasms
Pilot Study Comparing Systemic and Tissue Pharmacokinetics of Irinotecan and Metabolites after Hepatic Drug-Eluting Chemoembolization.
Neoplasms
Polymorphisms in CYP2A13 and UGT1A7 genes and head and neck cancer susceptibility in North Indians.
Neoplasms
Polymorphisms in SLCO1B1 and UGT1A1 are associated with sorafenib-induced toxicity.
Neoplasms
Polymorphisms in the UGT1A1 gene predict adverse effects of irinotecan in the treatment of gynecologic cancer in Japanese patients.
Neoplasms
Polymorphisms of the carcinogen detoxifying UDP-glucuronosyltransferase UGT1A7 in proximal digestive tract cancer.
Neoplasms
Polymorphisms of the human UDP-glucuronosyltransferase (UGT) 1A7 gene in colorectal cancer.
Neoplasms
Polymorphisms of UDP-glucuronosyltransferase and pharmacokinetics of irinotecan.
Neoplasms
Polymorphisms of UDP-glucuronosyltransferase gene and irinotecan toxicity: a pharmacogenetic analysis.
Neoplasms
Predictive biomarkers of chemotherapy efficacy in colorectal cancer: results from the UK MRC FOCUS trial.
Neoplasms
Pregnane x Receptor (PXR) expression in colorectal cancer cells restricts irinotecan chemosensitivity through enhanced SN-38 glucuronidation.
Neoplasms
Presence of T-275A and C-2152T Polymorphisms of the Promoter Region of Uridine Diphosphate-Glucuronosyltransferase 1A9 Increases Mortality From Digestive Tumors: Results After 10 Years of Follow-up in a Renal Transplant Population.
Neoplasms
Prevalence of the UGT1A1*28 promoter polymorphism and breast cancer risk among African American women in Memphis, TN.
Neoplasms
Principal xenobiotic-metabolizing enzyme systems in human head and neck squamous cell carcinoma.
Neoplasms
Protective effects of coffee against oxidative stress induced by the tobacco carcinogen benzo[?]pyrene.
Neoplasms
Quantitative Profiling of Human Renal UDP-glucuronosyltransferases and Glucuronidation Activity: A Comparison of Normal and Tumoral Kidney Tissues.
Neoplasms
Reduction of p53 by knockdown of the UGT1 locus in colon epithelial cells causes an increase in tumorigenesis.
Neoplasms
Regulation of UDP-Glucuronosyltransferases UGT2B4 and UGT2B7 by MicroRNAs in Liver Cancer Cells.
Neoplasms
Relationship between UGT1A1*6/*28 gene polymorphisms and the efficacy and toxicity of irinotecan-based chemotherapy.
Neoplasms
Relationship between UGT1A1*6/*28 polymorphisms and severe toxicities in Chinese patients with pancreatic or biliary tract cancer treated with irinotecan-containing regimens.
Neoplasms
Right and left-sided colon cancers - specificity of molecular mechanisms in tumorigenesis and progression.
Neoplasms
Role of glucocorticoid signaling in urothelial tumorigenesis: Inhibition by prednisone presumably through inducing glucocorticoid receptor transrepression.
Neoplasms
Role of UGT1A1*6 in irinogenetics in Asians.
Neoplasms
Role of vitamin D3 on the activity patterns of hepatic drug metabolizing enzymes in transplantable murine lymphoma.
Neoplasms
Roles of UGT2B7 C802T gene polymorphism on the efficacy of morphine treatment on cancer pain among the Chinese han population.
Neoplasms
Sacituzumab govitecan (IMMU-132), an anti-Trop-2-SN-38 antibody-drug conjugate for the treatment of diverse epithelial cancers: Safety and pharmacokinetics.
Neoplasms
Sequence variability and candidate gene analysis in two cancer patients with complex clinical outcomes during morphine therapy.
Neoplasms
Sequence variations in the UDP-glucuronosyltransferase 2B7 (UGT2B7) gene: identification of 10 novel single nucleotide polymorphisms (SNPs) and analysis of their relevance to morphine glucuronidation in cancer patients.
Neoplasms
Specificity of glucuronosyltransferase activity in the human cancer cell line LNCaP, evidence for the presence of at least two glucuronosyltransferase enzymes.
Neoplasms
Sulfoglucuronosyl paragloboside is a ligand for T cell adhesion: Regulation of sulfoglucuronosyl paragloboside expression via nuclear factor kappaB signaling.
Neoplasms
Suppression of AhR signaling pathway is associated with the down-regulation of UDP-glucuronosyltransferases during BBN-induced urinary bladder carcinogenesis in mice.
Neoplasms
The association between UGT1A7 polymorphism and cancer risk: A meta-analysis.
Neoplasms
The effect of UGT1A and UGT2B polymorphisms on colorectal cancer risk: haplotype associations and geneenvironment interactions.
Neoplasms
The Expression Profiles and Deregulation of UDP-Glycosyltransferase (UGT) Genes in Human Cancers and Their Association with Clinical Outcomes.
Neoplasms
The impact of UGT2B7 C802T and CYP3A4*1G polymorphisms on pain relief in cancer patients receiving oxycontin.
Neoplasms
The novel UGT1A9 intronic I399 polymorphism appears as a predictor of 7-ethyl-10-hydroxycamptothecin glucuronidation levels in the liver.
Neoplasms
The preventive factors for aspirin-induced peptic ulcer: aspirin ulcer and corpus atrophy.
Neoplasms
The role of SN-38 exposure, UGT1A1*28 polymorphism, and baseline bilirubin level in predicting severe irinotecan toxicity.
Neoplasms
The role of xenobiotic glucuronidating enzymes in drug resistance of tumour tissues and cells.
Neoplasms
The UDP-glucuronyltransferase inducers, phenobarbital and pregnenolone-16alpha-carbonitrile, enhance thyroid-follicular cell apoptosis: association with TGF-beta1 expression.
Neoplasms
The UGT2B28 Sex-steroid Inactivation Pathway Is a Regulator of Steroidogenesis and Modifies the Risk of Prostate Cancer Progression.
Neoplasms
Three novel single nucleotide polymorphisms in UGT1A10.
Neoplasms
Three novel single nucleotide polymorphisms in UGT1A9.
Neoplasms
Tissue biomarker development in a multicentre trial context: a feasibility study on the PETACC3 stage II and III colon cancer adjuvant treatment trial.
Neoplasms
Tissue-specific patterns of gene expression in the epithelium and stroma of normal colon in healthy individuals in an aspirin intervention trial.
Neoplasms
Tobacco carcinogen-detoxifying enzyme UGT1A7 and its association with orolaryngeal cancer risk.
Neoplasms
Toward individualized treatment: prediction of anticancer drug disposition and toxicity with pharmacogenetics.
Neoplasms
TPMT, UGT1A1 and DPYD: genotyping to ensure safer cancer therapy?
Neoplasms
Transplantation of Gunn rats with autologous fibroblasts expressing bilirubin UDP-glucuronosyltransferase: correction of genetic deficiency and tumor formation.
Neoplasms
Tumor necrosis factor-alpha up-regulates glucuronosyltransferase gene expression in human brain endothelial cells and promotes T-cell adhesion.
Neoplasms
Tumor-targeted delivery of 8-hydroxyquinoline.
Neoplasms
UDP glucuronosyltransferase 1A expression levels determine the response of colorectal cancer cells to the heat shock protein 90 inhibitor ganetespib.
Neoplasms
UDP-glucuronosyltransferase 1A10: activity against the tobacco-specific nitrosamine, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol, and a potential role for a novel UGT1A10 promoter deletion polymorphism in cancer susceptibility.
Neoplasms
UDP-glucuronosyltransferase 2B15 (UGT2B15) and UGT2B17 enzymes are major determinants of the androgen response in prostate cancer LNCaP cells.
Neoplasms
UDP-glucuronosyltransferase and sulfotransferase polymorphisms, sex hormone concentrations, and tumor receptor status in breast cancer patients.
Neoplasms
UDP-glucuronosyltransferase polymorphisms affect diethylnitrosamine-induced carcinogenesis in humanized transgenic mice.
Neoplasms
UDP-glucuronosyltransferases and biochemical recurrence in prostate cancer progression.
Neoplasms
UGT1A and TYMS genetic variants predict toxicity and response of colorectal cancer patients treated with first-line irinotecan and fluorouracil combination therapy.
Neoplasms
UGT1A1 Gene Polymorphism Predicts Irinotecan-Induced Severe Neutropenia and Diarrhea in Chinese Cancer Patients.
Neoplasms
UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancer.
Neoplasms
UGT1A1 genotype-dependent dose adjustment of belinostat in patients with advanced cancers using population pharmacokinetic modeling and simulation.
Neoplasms
UGT1A1 genotype-specific phase I and pharmacokinetic study for combination chemotherapy with irinotecan and cisplatin: a Saitama Tumor Board study.
Neoplasms
UGT1A1 Guided Cancer Therapy: Review of the Evidence and Considerations for Clinical Implementation.
Neoplasms
UGT1A1 haplotypes associated with reduced glucuronidation and increased serum bilirubin in irinotecan-administered Japanese patients with cancer.
Neoplasms
UGT1A1 polymorphism has a prognostic effect in patients with stage IB or II uterine cervical cancer and one or no metastatic pelvic nodes receiving irinotecan chemotherapy: a retrospective study.
Neoplasms
UGT1A1 polymorphisms are important determinants of dietary carcinogen detoxification in the liver.
Neoplasms
UGT1A1 polymorphisms in cancer: impact on irinotecan treatment.
Neoplasms
UGT1A1 promoter genotype correlates with SN-38 pharmacokinetics, but not severe toxicity in patients receiving low-dose irinotecan.
Neoplasms
UGT1A1 regulatory variant with potential effect on efficacy of HIV and cancer drugs commonly prescribed in South Africa.
Neoplasms
UGT1A1*28 polymorphism in ovarian cancer patients.
Neoplasms
UGT1A1*6 polymorphism is most predictive of severe neutropenia induced by irinotecan in Japanese cancer patients.
Neoplasms
UGT1A1*6 polymorphisms are correlated with irinotecan-induced toxicity: a system review and meta-analysis in Asians.
Neoplasms
UGT1A1, UGT1A6 and UGT1A7 Genetic Analysis: Repercussion for Irinotecan Pharmacogenetics in the São Miguel Island Population (Azores, Portugal).
Neoplasms
UGT1A7 and UGT1A9 polymorphisms predict response and toxicity in colorectal cancer patients treated with capecitabine/irinotecan.
Neoplasms
UGT2B17 and miR-224 contribute to hormone dependency trends in adenocarcinoma and squamous cell carcinoma of esophagus.
Neoplasms
UGT2B17 Expedites Progression of Castration-Resistant Prostate Cancers by Promoting Ligand-Independent AR Signaling.
Neoplasms
Uridine 5'-diphospho-glucuronosyltransferase genetic polymorphisms and response to cancer chemotherapy.
Neoplasms
Uridine diphosphate glucuronosyltransferase (UGT) 1A1 and irinotecan: practical pharmacogenomics arrives in cancer therapy.
Neoplasms
Uridine diphosphoglucuronosyltransferase pharmacogenetics and cancer.
Neoplasms
Variability and function of family 1 uridine-5'-diphosphate glucuronosyltransferases (UGT1A).
Neoplasms
Variability in UDP-glucuronosyltransferase genes and morphine metabolism: observations from a cross-sectional multicenter study in advanced cancer patients with pain.
Neoplasms
Virtual Clinical Studies to Examine the Probability Distribution of the AUC at Target Tissues Using Physiologically-Based Pharmacokinetic Modeling: Application to Analyses of the Effect of Genetic Polymorphism of Enzymes and Transporters on Irinotecan Induced Side Effects.
Neoplasms
Vitamin C and aloe vera supplementation protects from chemical hepatocarcinogenesis in the rat.
Neoplasms
Whole-exome Sequencing of Prostate Cancer in Sardinian Identify Recurrent UDP-glucuronosyltransferase Amplifications.
Neoplasms
Xenobiotic metabolizing enzymes in genetically and chemically initiated mouse liver tumors.
Neoplasms
[A Case of Unresectable Advanced Rectal Cancer with a Pancreatic Tumor That Was Successfully Treated with FOLFIRINOX].
Neoplasms
[Association between genetic polymorphisms of metabolic enzymes and susceptibility of colorectal cancer]
Neoplasms
[Glucuronic acid, glucuronyltransferase and estrogens in breast cancer and precancer]
Neoplasms
[Influence of genetic polymorphisms in UGT1A1, UGT1A7 and UGT1A9 on the pharmacokynetics of irinotecan, SN-38 and SN-38G.]
Neoplasms
[Interest of UGT1A1 genotyping within digestive cancers treatment by irinotecan].
Neoplasms
[Pharmacogenomic research for avoiding adverse reactions by anti-cancer drugs].
Neoplasms
[The biological point of view on pharmacogenetics of anticancer agents in colorectal cancer]
Nephrolithiasis
Single-nucleotide polymorphisms in the UDP-glucuronosyltransferase 1A-3' untranslated region are associated with atazanavir-induced nephrolithiasis in patients with HIV-1 infection: a pharmacogenetic study.
Neuralgia
Mechanism for Increased Expression of UGT2B in the Liver of Mice with Neuropathic Pain.
Neuroblastoma
Endogenous Morphine in SH-SY5Y Cells and the Mouse Cerebellum.
Neuroendocrine Tumors
Pharmacogenetic impact of UGT1A1 polymorphisms on pulmonary neuroendocrine tumours treated with metronomic irinotecan-based chemotherapy in Chinese populations.
Neuroinflammatory Diseases
Tumor necrosis factor-alpha up-regulates glucuronosyltransferase gene expression in human brain endothelial cells and promotes T-cell adhesion.
Neutropenia
A Multicenter Clinical Phase II Study of FOLFOXIRI Plus Bevacizumab as First-line Therapy in Patients With Metastatic Colorectal Cancer: QUATTRO Study.
Neutropenia
A multicenter phase II study of personalized FOLFIRI-cetuximab for safe dose intensification.
Neutropenia
A prospective study of XELIRI plus bevacizumab as a first-line therapy in Japanese patients with unresectable or recurrent colorectal cancer (KSCC1101).
Neutropenia
ABC transporter polymorphisms are associated with irinotecan pharmacokinetics and neutropenia.
Neutropenia
An internally and externally validated nomogram for predicting the risk of irinotecan-induced severe neutropenia in advanced colorectal cancer patients.
Neutropenia
Association between the low-dose irinotecan regimen-induced occurrence of grade 4 neutropenia and genetic variants of UGT1A1 in patients with gynecological cancers.
Neutropenia
Association of carboxylesterase 1A genotypes with irinotecan pharmacokinetics in Japanese cancer patients.
Neutropenia
Association of UGT1A1*28 polymorphisms with irinotecan-induced toxicities in colorectal cancer: a meta-analysis in Caucasians.
Neutropenia
Associations between UGT1A1*6 or UGT1A1*6/*28 polymorphisms and irinotecan-induced neutropenia in Asian cancer patients.
Neutropenia
Can UGT1A1 genotyping reduce morbidity and mortality in patients with metastatic colorectal cancer treated with irinotecan? An evidence-based review.
Neutropenia
Clinical and pharmacogenetic determinants of 5-fluorouracyl/leucovorin/irinotecan toxicity: Results of the PETACC-3 trial.
Neutropenia
Clinical and pharmacogenetic factors associated with irinotecan toxicity.
Neutropenia
Clinical significance of UGT1A1 gene polymorphisms on irinotecan-based regimens as the treatment in metastatic colorectal cancer.
Neutropenia
Clinical usefulness of testing for UDP glucuronosyltransferase 1 family, polypeptide A1 polymorphism prior to the inititation of irinotecan-based chemotherapy.
Neutropenia
Correlation between plasma concentration ratios of SN-38 glucuronide and SN-38 and neutropenia induction in patients with colorectal cancer and wild-type UGT1A1 gene.
Neutropenia
Correlation between UGT1A1 gene polymorphism and irinotecan chemotherapy in metastatic colorectal cancer: a study from Guangxi Zhuang.
Neutropenia
Distribution of the UGT1A1*28 polymorphism in Caucasian and Asian populations in the US: a genomic analysis of 138 healthy individuals.
Neutropenia
Erratum to: UDP-glucuronosyltransferase 1A1*6 and *28 polymorphisms as indicators of initial dose level of irinotecan to reduce risk of neutropenia in patients receiving FOLFIRI for colorectal cancer.
Neutropenia
Genetic determinants of cancer drug efficacy and toxicity: practical considerations and perspectives.
Neutropenia
Genetic variants in the UDP-glucuronosyltransferase 1A1 gene predict the risk of severe neutropenia of irinotecan.
Neutropenia
Increased frequency of uridine diphosphate glucuronosyltransferase 1A1 7/7 in patients experiencing severe irinotecan-induced toxicities.
Neutropenia
Influence of UGT1A1 polymorphism on etoposide plus platinum-induced neutropenia in Japanese patients with small-cell lung cancer.
Neutropenia
Pharmacogenetic determinants of outcomes on triplet hepatic artery infusion and intravenous cetuximab for liver metastases from colorectal cancer (European trial OPTILIV, NCT00852228).
Neutropenia
Pharmacogenetics and irinotecan therapy.
Neutropenia
Pharmacometrics-Based Considerations for the Design of a Pharmacogenomic Clinical Trial Assessing Irinotecan Safety.
Neutropenia
Phase II study of a triplet regimen of S-1 combined with irinotecan and oxaliplatin in patients with metastatic gastric cancer: clinical and pharmacogenetic results.
Neutropenia
Phase III Trial of Irinotecan/Cisplatin Compared With Etoposide/Cisplatin in Extensive-Stage Small-Cell Lung Cancer: Clinical and Pharmacogenomic Results From SWOG S0124.
Neutropenia
Prolonged Neutropenia after Irinotecan-based Chemotherapy in a Child with polymorphisms of UGT1A1 and SLCO1B1.
Neutropenia
Recommendations from the EGAPP Working Group: can UGT1A1 genotyping reduce morbidity and mortality in patients with metastatic colorectal cancer treated with irinotecan?
Neutropenia
Refining the UGT1A Haplotype Associated with Irinotecan-Induced Hematological Toxicity in Metastatic Colorectal Cancer Patients Treated with 5-Fluorouracil/Irinotecan-Based Regimens.
Neutropenia
Regimen Selection for First-line FOLFIRI and FOLFOX Based on UGT1A1 Genotype and Physical Background is Feasible in Japanese Patients with Advanced Colorectal Cancer.
Neutropenia
Sacituzumab govitecan (IMMU-132), an anti-Trop-2-SN-38 antibody-drug conjugate for the treatment of diverse epithelial cancers: Safety and pharmacokinetics.
Neutropenia
Severe irinotecan-induced toxicity in a patient with UGT1A1 28 and UGT1A1 6 polymorphisms.
Neutropenia
The role of SN-38 exposure, UGT1A1*28 polymorphism, and baseline bilirubin level in predicting severe irinotecan toxicity.
Neutropenia
UDP-glucuronosyltransferase 1A1*6 and *28 polymorphisms as indicators of initial dose level of irinotecan to reduce risk of neutropenia in patients receiving FOLFIRI for colorectal cancer.
Neutropenia
UGT1A1 6/28 polymorphisms could predict irinotecan-induced severe neutropenia not diarrhea in Chinese colorectal cancer patients.
Neutropenia
UGT1A1 Gene Polymorphism Predicts Irinotecan-Induced Severe Neutropenia and Diarrhea in Chinese Cancer Patients.
Neutropenia
UGT1A1 Gene Polymorphisms and the Toxicities of FOLFIRI in Chinese Han Patients with Gastrointestinal Cancer.
Neutropenia
UGT1A1 genotyping and neutropenia risk.
Neutropenia
UGT1A1 Guided Cancer Therapy: Review of the Evidence and Considerations for Clinical Implementation.
Neutropenia
UGT1A1 polymorphisms in rectal cancer associated with the efficacy and toxicity of preoperative chemoradiotherapy using irinotecan.
Neutropenia
UGT1A1*28 genotype predicts gastrointestinal toxicity in patients treated with intermediate-dose irinotecan.
Neutropenia
UGT1A1*6 polymorphism is most predictive of severe neutropenia induced by irinotecan in Japanese cancer patients.
Neutropenia
Uridine diphosphate glucuronosyltransferase 1A1.
Neutropenia
Usefulness of one-point plasma SN-38G/SN-38 concentration ratios as a substitute for UGT1A1 genetic information after irinotecan administration.
Neutropenia
Utility of Pretreatment Bilirubin Level and UGT1A1 Polymorphisms in Multivariate Predictive Models of Neutropenia Associated with Irinotecan Treatment in Previously Untreated Patients with Colorectal Cancer.
Neutropenia
Virtual Clinical Studies to Examine the Probability Distribution of the AUC at Target Tissues Using Physiologically-Based Pharmacokinetic Modeling: Application to Analyses of the Effect of Genetic Polymorphism of Enzymes and Transporters on Irinotecan Induced Side Effects.
Neutropenia
XELIRI compared with FOLFIRI as a second-line treatment in patients with metastatic colorectal cancer.
Neutropenia
[A prevalent genetic variety of UDP-glycuronosyl transferase predicts high risk of irinotecan toxicity]
Neutropenia
[Association of UGT1A1 (*28, *60 and * 93) polymorphism with the adverse reactions of irinotecan chemotherapy in extensive stage small cell lung cancer].
Neutropenia
[Examination of UGT1A1 polymorphisms and irinotecan-induced neutropenia in patients with Colorectal cancer].
Neutropenia
[The biological point of view on pharmacogenetics of anticancer agents in colorectal cancer]
Neutropenia
[Two cases of advanced colorectal cancer with UGT1A1*28 homozygosity treated by FOLFIRI]
Neutropenia
[UGT1A1 Genotyping for Proper Use of Irinotecan].
Non-alcoholic Fatty Liver Disease
Acetaminophen pharmacokinetics in children with nonalcoholic fatty liver disease.
Non-alcoholic Fatty Liver Disease
Altered UDP-glucuronosyltransferase and sulfotransferase expression and function during progressive stages of human nonalcoholic fatty liver disease.
Non-alcoholic Fatty Liver Disease
Genetically Regulated Bilirubin and Risk of Non-alcoholic Fatty Liver Disease: A Mendelian Randomization Study.
Non-alcoholic Fatty Liver Disease
Role of UDP-Glucuronosyltransferase 1A1 in the Metabolism and Pharmacokinetics of Silymarin Flavonolignans in Patients with HCV and NAFLD.
Non-alcoholic Fatty Liver Disease
Variants in the UGT1A1 gene and the risk of pediatric nonalcoholic fatty liver disease.
Obesity
Impact of obesity on accumulation of the toxic irinotecan metabolite, SN-38, in mice.
Obesity
Obstetric Obesity is Associated with Neonatal Hyperbilirubinemia with High Prevalence in Native Hawaiians and Pacific Island Women.
Obesity
Oral Morphine Pharmacokinetic in Obesity: The Role of P-Glycoprotein, MRP2, MRP3, UGT2B7, and CYP3A4 Jejunal Contents and Obesity-Associated Biomarkers.
Obesity, Morbid
Genome-wide analysis of hepatic lipid content in extreme obesity.
Obesity, Morbid
Obstetric Obesity is Associated with Neonatal Hyperbilirubinemia with High Prevalence in Native Hawaiians and Pacific Island Women.
Osteoporosis
Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis.
Osteoporosis
Homozygous deletion of the UGT2B17 gene is not associated with osteoporosis risk in elderly Caucasian women.
Osteoporosis
Polymorphisms of estrogen metabolism-related genes ESR1, UGT2B17, and UGT1A1 are not associated with osteoporosis in surgically menopausal Japanese women.
Osteoporosis
Potential influence of UGT1A8 genotype on osteoporosis and breast cancer treatment outcome.
Osteoporosis
Raloxifene glucuronidation in liver and intestinal microsomes of humans and monkeys: contribution of UGT1A1, UGT1A8 and UGT1A9.
Osteoporosis
The importance of the UGT1A1 variants in the development of osteopenia and osteoporosis in postmenopausal women.
Ovarian Neoplasms
Correlation of UGT1A1 and ERCC1 gene polymorphisms with the outcome of combined irinotecan plus cisplatin treatment in recurrent ovarian cancer.
Ovarian Neoplasms
Polymorphisms in the UGT1A1 gene predict adverse effects of irinotecan in the treatment of gynecologic cancer in Japanese patients.
Ovarian Neoplasms
UGT1A1 polymorphism as a prognostic indicator of stage I ovarian clear cell carcinoma patients treated with irinotecan.
Ovarian Neoplasms
[Study of irinotecan-induced toxicity and its correlation to UGT1A1 gene promoter polymorphisms].
Pancreatic Diseases
Polymorphisms of UDP-glucuronosyltransferase 1A7 are not involved in pancreatic diseases.
Pancreatic Diseases
UDP glucuronosyltransferase (UGT1A7) gene polymorphisms increase the risk of chronic pancreatitis and pancreatic cancer.
Pancreatic Neoplasms
Association of Genetic Polymorphisms in UDP-Glucuronosyltransferases 2B17 with the Risk of Pancreatic Cancer in Chinese Han Population.
Pancreatic Neoplasms
FOLFIRINOX in advanced pancreatic cancer patients with the double-variant type of UGT1A1 *28 and *6 polymorphism: a multicenter, retrospective study.
Pancreatic Neoplasms
Impact of UGT1A1 genetic polymorphism on toxicity in unresectable pancreatic cancer patients undergoing FOLFIRINOX.
Pancreatic Neoplasms
Increased UGT1A3 and UGT1A7 Expression is Associated with Pancreatic Cancer.
Pancreatic Neoplasms
Lack of association between UGT1A7, UGT1A9, ARP, SPINK1 and CFTR gene polymorphisms and pancreatic cancer in Italian patients.
Pancreatic Neoplasms
Polymorphisms in UGT2B4 and susceptibility to pancreatic cancer.
Pancreatic Neoplasms
Polymorphisms of UDP-glucuronosyltransferase 1A7 are not involved in pancreatic diseases.
Pancreatic Neoplasms
UDP glucuronosyltransferase (UGT1A7) gene polymorphisms increase the risk of chronic pancreatitis and pancreatic cancer.
Pancreatic Neoplasms
[A Case of Unresectable Advanced Rectal Cancer with a Pancreatic Tumor That Was Successfully Treated with FOLFIRINOX].
Pancreatic Neoplasms
[FOLFIRINOX for Locally Advanced and Recurrent Pancreatic Cancer with UGT1A1 *6 and or UGT1A1*28 Polymorphisms-A Report of Two Cases].
Pancreatitis
Polymorphisms of UDP-glucuronosyltransferase 1A7 are not involved in pancreatic diseases.
Pancreatitis, Chronic
Polymorphisms of UDP-glucuronosyltransferase 1A7 are not involved in pancreatic diseases.
Pancreatitis, Chronic
UDP glucuronosyltransferase (UGT1A7) gene polymorphisms increase the risk of chronic pancreatitis and pancreatic cancer.
Pancreatitis, Chronic
UGT1A7 polymorphisms in chronic pancreatitis: an example of genotyping pitfalls.
Parkinson Disease
Association of UDP-glucuronosyltransferase 1A9 polymorphisms with adverse reactions to catechol-O-methyltransferase inhibitors in Parkinson's disease patients.
Parkinson Disease
The N6-methyladenosine modification posttranscriptionally regulates hepatic UGT2B7 expression.
Peptic Ulcer
Genetic polymorphisms in UDP-glucuronosyltransferase 1A6 are not associated with NSAIDs-related peptic ulcer haemorrhage.
Peptic Ulcer
Protective effect and mechanisms of action of Mongolian medicine Sulongga-4 on pyloric ligation-induced gastroduodenal ulcer in rats.
Peripheral Arterial Disease
Association between the UGT1A1 TA-repeat polymorphism and bilirubin concentration in patients with intermittent claudication: results from the CAVASIC study.
Peripheral Nervous System Diseases
[A Case of Unresectable Advanced Rectal Cancer with a Pancreatic Tumor That Was Successfully Treated with FOLFIRINOX].
Pneumonia
Influence of SLCO1B1 521T>C, UGT2B7 802C>T and IMPDH1 -106G>A Genetic Polymorphisms on Mycophenolic Acid Levels and Adverse Reactions in Chinese Autoimmune Disease Patients.
Pneumonia, Pneumocystis
Influence of SLCO1B1 521T>C, UGT2B7 802C>T and IMPDH1 -106G>A Genetic Polymorphisms on Mycophenolic Acid Levels and Adverse Reactions in Chinese Autoimmune Disease Patients.
Polycystic Ovary Syndrome
The correlation between UDP-glucuronosyltransferase polymorphisms and environmental endocrine disruptors levels in polycystic ovary syndrome patients.
Pre-Eclampsia
Placental profiling of UGT1A enzyme expression and activity and interactions with preeclampsia at term.
Pre-Eclampsia
[Refinement and role of the diagnosis of Gilbert disease with molecular biology]
Precursor Cell Lymphoblastic Leukemia-Lymphoma
A personalized approach to cancer treatment: how biomarkers can help.
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Effects of prednisone and genetic polymorphisms on etoposide disposition in children with acute lymphoblastic leukemia.
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Outcome and toxicities associated to chemotherapy in children with acute lymphoblastic leukemia and Gilbert syndrome. Usefulness of UGT1A1 mutational screening.
Premature Birth
Risk factors for severe hyperbilirubinemia in neonates.
Premature Birth
The effect of premature and delayed birth on the development of UDP-glucuronosyltransferase activities towards bilirubin, morphine and testosterone in the rat.
Premature Birth
The prenatal and postnatal development of UDP-glucuronyltransferase activity towards bilirubin and the effect of premature birth on this activity in the human liver.
Propionic Acidemia
Natural variation in a glucuronosyltransferase modulates propionate sensitivity in a C. elegans propionic acidemia model.
Prostatic Hyperplasia
Differential Expression of the Androgen-Conjugating UGT2B15 and UGT2B17 Enzymes in Prostate Tumor Cells during Cancer Progression.
Prostatic Hyperplasia
Genetic variations in UGT2B28, UGT2B17, UGT2B15 genes and the risk of prostate cancer: A case-control study.
Prostatic Hyperplasia
Lack of association between the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene polymorphism and the risk of benign prostatic hyperplasia in Caucasian men.
Prostatic Neoplasms
A novel polymorphism in a forkhead box A1 (FOXA1) binding site of the human UDP glucuronosyltransferase 2B17 gene modulates promoter activity and is associated with altered levels of circulating androstane-3?,17?-diol glucuronide.
Prostatic Neoplasms
A polymorphism in the UDP-Glucuronosyltransferase 2B15 gene (D85Y) is not associated with prostate cancer risk.
Prostatic Neoplasms
Activators of the farnesoid X receptor negatively regulate androgen glucuronidation in human prostate cancer LNCAP cells.
Prostatic Neoplasms
An allele-specific polymerase chain reaction method for the determination of the D85Y polymorphism in the human UDP-glucuronosyltransferase 2B15 gene in a case-control study of prostate cancer.
Prostatic Neoplasms
Androgen glucuronidation: an unexpected target for androgen deprivation therapy, with prognosis and diagnostic implications.
Prostatic Neoplasms
Androgen metabolism genes in prostate cancer health disparities.
Prostatic Neoplasms
Androgen receptor mediates the expression of UDP-glucuronosyltransferase 2 B15 and B17 genes.
Prostatic Neoplasms
Androgen-independent growth in LNCaP cell lines and steroid uridine diphosphate-glucuronosyltransferase expression.
Prostatic Neoplasms
Asp85tyr polymorphism in the udp-glucuronosyltransferase (UGT) 2B15 gene and the risk of prostate cancer.
Prostatic Neoplasms
Association between polymorphisms in HSD3B1 and UGT2B17 and prostate cancer risk.
Prostatic Neoplasms
Association of the polymorphisms of genes involved in androgen metabolism and signaling pathways with familial prostate cancer risk in a Japanese population.
Prostatic Neoplasms
Association of uridine diphosphate-glucuronosyltransferase 2B gene variants with serum glucuronide levels and prostate cancer risk.
Prostatic Neoplasms
Calcitrol (1alpha,25-dihydroxyvitamin D3) inhibits androgen glucuronidation in prostate cancer cells.
Prostatic Neoplasms
Characterisations of human prostate stem cells reveal deficiency in class I UGT enzymes as a novel mechanism for castration-resistant prostate cancer.
Prostatic Neoplasms
Chromosomal structural variations during progression of a prostate epithelial cell line to a malignant metastatic state inactivate the NF2, NIPSNAP1, UGT2B17 and LPIN2 genes.
Prostatic Neoplasms
Deletion polymorphism of the UGT2B17 gene is associated with increased risk for prostate cancer and correlated to gene expression in the prostate.
Prostatic Neoplasms
Deletion polymorphism of UDP-glucuronosyltransferase 2B17 and risk of prostate cancer in African American and Caucasian men.
Prostatic Neoplasms
Differential Expression of the Androgen-Conjugating UGT2B15 and UGT2B17 Enzymes in Prostate Tumor Cells during Cancer Progression.
Prostatic Neoplasms
Effect of interleukins on UGT2B15 and UGT2B17 steroid uridine diphosphate-glucuronosyltransferase expression and activity in the LNCaP cell line.
Prostatic Neoplasms
Epigenetic regulation of steroid inactivating UDP-glucuronosyltransferases by microRNAs in prostate cancer.
Prostatic Neoplasms
Evidence for a role of glucuronosyltransferase in the regulation of androgen action in the human prostatic cancer cell line LNCaP.
Prostatic Neoplasms
Expression of UDP Glucuronosyltransferases 2B15 and 2B17 is associated with methylation status in prostate cancer cells.
Prostatic Neoplasms
Forkhead box protein A1 regulates UDP glucuronosyltransferase 2B15 gene transcription in LNCaP prostate cancer cells.
Prostatic Neoplasms
Genetic polymorphisms in the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene and prostate cancer risk in Caucasian men.
Prostatic Neoplasms
Genetic variations in UDP-glucuronosyltransferase 2B15 in a Korean population.
Prostatic Neoplasms
Genetic variations in UGT2B28, UGT2B17, UGT2B15 genes and the risk of prostate cancer: A case-control study.
Prostatic Neoplasms
Increased UDP-glucuronosyltransferase activity and decreased prostate specific antigen production by biochanin A in prostate cancer cells.
Prostatic Neoplasms
Intergenic Splicing between Four Adjacent UGT Genes (2B15, 2B29P2, 2B17, 2B29P1) Gives Rise to Variant UGT Proteins That Inhibit Glucuronidation via Protein-Protein Interactions.
Prostatic Neoplasms
Multiple roles for udp-glucuronosyltransferase (UGT)2B15 and UGT2B17 enzymes in androgen metabolism and prostate cancer evolution.
Prostatic Neoplasms
Novel associations of UDP-glucuronosyltransferase 2B gene variants with prostate cancer risk in a multiethnic study.
Prostatic Neoplasms
Polymorphisms of Estrogen Metabolism-Related Genes and Prostate Cancer Risk in Two Populations of African Ancestry.
Prostatic Neoplasms
Promoter length polymorphism in UGT1A1 and the risk of sporadic colorectal cancer.
Prostatic Neoplasms
Prostate cancer and polymorphism D85Y in gene for dihydrotestosterone degrading enzyme UGT2B15: Frequency of DD homozygotes increases with Gleason Score.
Prostatic Neoplasms
Prostate Cancer with Variants in CYP17 and UGT2B17 Genes: A Meta-Analysis.
Prostatic Neoplasms
Regulation of Human UGT2B15 and UGT2B17 by miR-376c in Prostate Cancer Cell Lines.
Prostatic Neoplasms
Regulation of steroid glucuronosyltransferase activities and transcripts by androgen in the human prostatic cancer LNCaP cell line.
Prostatic Neoplasms
Regulation of UDP-Glucuronosyltransferase 2B15 by miR-331-5p in Prostate Cancer Cells Involves Canonical and Noncanonical Target Sites.
Prostatic Neoplasms
Repeat polymorphisms in estrogen metabolism genes and prostate cancer risk: results from the Prostate Cancer Prevention Trial.
Prostatic Neoplasms
Steroidogenic enzymes and stem cell markers are up-regulated during androgen deprivation in prostate cancer.
Prostatic Neoplasms
The UGT2B17 gene deletion is not associated with prostate cancer risk.
Prostatic Neoplasms
The UGT2B17 gene deletion polymorphism and risk of prostate cancer A case-control study in Caucasians.
Prostatic Neoplasms
The UGT2B17 gene deletion polymorphism and risk of prostate cancer: A case-control study in Caucasians.
Prostatic Neoplasms
The UGT2B28 Sex-steroid Inactivation Pathway Is a Regulator of Steroidogenesis and Modifies the Risk of Prostate Cancer Progression.
Prostatic Neoplasms
UDP-glucuronosyltransferase 2B15 (UGT2B15) and UGT2B17 enzymes are major determinants of the androgen response in prostate cancer LNCaP cells.
Prostatic Neoplasms
UDP-glucuronosyltransferase Enzymes in Prostate Cancer Progression: Is Only Androgen Catabolism Involved?
Prostatic Neoplasms
UDP-glucuronosyltransferases and biochemical recurrence in prostate cancer progression.
Prostatic Neoplasms
UGT2B17 Expedites Progression of Castration-Resistant Prostate Cancers by Promoting Ligand-Independent AR Signaling.
Prostatic Neoplasms
UGT2B17 Polymorphism and Risk of Prostate Cancer: A Meta-Analysis.
Prostatic Neoplasms
Uridine diphosphate-glucuronosyltransferase 2B15 D85Y gene polymorphism is associated with lower prostate cancer risk: a systematic review and meta-analysis.
Prostatic Neoplasms
Whole-exome Sequencing of Prostate Cancer in Sardinian Identify Recurrent UDP-glucuronosyltransferase Amplifications.
Protein Deficiency
Effect of a dietary protein deficiency on the development of hepatic drug-metabolizing enzymes in young rats.
Protein Deficiency
Effects of protein deficiency on uridine diphosphate glucuronyltransferase activity and phospholipid composition of rat liver microsomal fraction.
Protein Deficiency
The phospholipid-dependence of uridine diphosphate glucuronyltransferase. Effect of protein deficiency on the phospholipid composition and enzyme activity of rat liver microsomal fraction.
Protein Deficiency
[Effect of protein deficiency and captan on the activity of alkaline phosphatase and UDP-Glucuronyltransferase in rat liver]
Pulmonary Disease, Chronic Obstructive
Drug metabolism in severe chronic obstructive pulmonary disease: A phenotyping cocktail study.
Pulmonary Disease, Chronic Obstructive
Prediction of new targets and mechanisms for quercetin in the treatment of pancreatic cancer, colon cancer, and rectal cancer.
Pyelonephritis
UGT1A1 promoter polymorphism as a predisposing factor of hyperbilirubinaemia in neonates with acute pyelonephritis.
Rectal Neoplasms
An expansion study of genotype-driven weekly irinotecan and capecitabine in combination with neoadjuvant radiotherapy for locally advanced rectal cancer with UGT1A1 *1*1 genotype.
Rectal Neoplasms
Multicenter, Randomized, Phase III Trial of Neoadjuvant Chemoradiation With Capecitabine and Irinotecan Guided by UGT1A1 Status in Patients With Locally Advanced Rectal Cancer.
Rectal Neoplasms
The effect of UGT1A and UGT2B polymorphisms on colorectal cancer risk: haplotype associations and geneenvironment interactions.
Rectal Neoplasms
UGT1A1 polymorphisms in rectal cancer associated with the efficacy and toxicity of preoperative chemoradiotherapy using irinotecan.
Rectal Neoplasms
[A Case of Unresectable Advanced Rectal Cancer with a Pancreatic Tumor That Was Successfully Treated with FOLFIRINOX].
Respiratory Insufficiency
Prolonged central apnoea after intravenous morphine administration in a 12-year-old male with a UGT1A1 loss-of-function polymorphism.
Rhabdomyosarcoma, Alveolar
Life-Threatening Irinotecan-Induced Toxicity in an Adult Patient with Alveolar Rhabdomyosarcoma: The Role of a UGT1A1 Polymorphism.
Sarcoma
Clinicopathological observation of primary lung enteric adenocarcinoma and its response to chemotherapy: A case report and review of the literature.
Seizures
Developmental hyperbilirubinemia and CNS toxicity in mice humanized with the UDP glucuronosyltransferase 1 (UGT1) locus.
Seizures
Developmental onset of bilirubin-induced neurotoxicity involves Toll-like receptor 2-dependent signaling in humanized UDP-glucuronosyltransferase1 mice.
Seizures
Early post-traumatic seizures are associated with valproic acid plasma concentrations and UGT1A6/CYP2C9 genetic polymorphisms in patients with severe traumatic brain injury.
Seizures
Effect of status epilepticus on expression of brain UDP-glucuronosyltransferase 1a in rats.
Seizures
Effects of UGT1A9 genetic polymorphisms on monohydroxylated derivative of oxcarbazepine concentrations and oxcarbazepine monotherapeutic efficacy in Chinese patients with epilepsy.
Seizures
Effects of UGT2B7, SCN1A and CYP3A4 on the therapeutic response of sodium valproate treatment in children with generalized seizures.
Seizures
Reduced Myelination and Increased Glia Reactivity Resulting from Severe Neonatal Hyperbilirubinemia.
Sepsis
Metabolism-mediated drug interaction potential of HS-23, a new herbal drug for the treatment of sepsis in human hepatocytes and liver microsomes.
Siderosis
Pyrimidine-5'-nucleotidase Campinas, a new mutation (p.R56G) in the NT5C3 gene associated with pyrimidine-5'-nucleotidase type I deficiency and influence of Gilbert's Syndrome on clinical expression.
Sleep Initiation and Maintenance Disorders
Insomnia affects the levels of plasma bilirubin and protein metabolism: an observational study and GWGEIS in UK Biobank cohort.
Small Cell Lung Carcinoma
Association of nephrotoxicity during platinum-etoposide doublet therapy with UGT1A1 polymorphisms in small cell lung cancer patients.
Small Cell Lung Carcinoma
Cisplatin combined with irinotecan or etoposide for untreated extensive-stage small cell lung cancer: A multicenter randomized controlled clinical trial.
Small Cell Lung Carcinoma
UGT1A1 Gene Polymorphisms in Patients with Small Cell Lung Cancer Treated with Irinotecan-Platinum Doublet Chemotherapy and Their Association with Gastrointestinal Toxicity and Overall Survival.
Small Cell Lung Carcinoma
[Association of UGT1A1 (*28, *60 and * 93) polymorphism with the adverse reactions of irinotecan chemotherapy in extensive stage small cell lung cancer].
Spondylitis, Ankylosing
UGT2B17 copy number gain in a large ankylosing spondylitis multiplex family.
Squamous Cell Carcinoma of Head and Neck
Association between UGT1A1 Polymorphism and Risk of Laryngeal Squamous Cell Carcinoma.
Starvation
Effect of fasting on substrate specificity of rat liver UDP-glucuronosyltransferase.
Starvation
Molecular basis of bilirubin UDP-glucuronosyltransferase induction in spontaneously diabetic rats, acetone-treated rats and starved rats.
Status Epilepticus
Effect of status epilepticus on expression of brain UDP-glucuronosyltransferase 1a in rats.
Stomach Neoplasms
Association between UGT1A1 gene polymorphism and safety and efficacy of irinotecan monotherapy as the third-line treatment for advanced gastric cancer.
Stomach Neoplasms
Bioinformatic analysis suggests that UGT2B15 activates the Hippo?YAP signaling pathway leading to the pathogenesis of gastric cancer.
Stomach Neoplasms
Clinical significance of UGT1A1 polymorphism and expression of ERCC1, BRCA1, TYMS, RRM1, TUBB3, STMN1 and TOP2A in gastric cancer.
Stomach Neoplasms
Comprehensive analysis of excision repair complementation group 1, glutathione S-transferase, thymidylate synthase and uridine diphosphate glucuronosyl transferase 1A1 polymorphisms predictive for treatment outcome in patients with advanced gastric cancer treated with FOLFOX or FOLFIRI.
Stomach Neoplasms
Differential expression of the UGT1A family of genes in stomach cancer tissues.
Stomach Neoplasms
Impact of single-heterozygous UGT1A1 on the clinical outcomes of irinotecan monotherapy after fluoropyrimidine and platinum-based combination therapy for gastric cancer: a multicenter retrospective study.
Stomach Neoplasms
Phase II and UGT1A1 genotype study of irinotecan dose escalation as salvage therapy for advanced gastric cancer.
Stomach Neoplasms
Phase II and UGT1A1 Polymorphism Study of Two Different Irinotecan Dosages Combined with Cisplatin as First-Line Therapy for Advanced Gastric Cancer.
Stomach Neoplasms
Phase II study of a triplet regimen of S-1 combined with irinotecan and oxaliplatin in patients with metastatic gastric cancer: clinical and pharmacogenetic results.
Stomach Neoplasms
Polymorphisms of the carcinogen detoxifying UDP-glucuronosyltransferase UGT1A7 in proximal digestive tract cancer.
Stomach Neoplasms
The comparison between UGT1A1 single heterozygous and wild-type regarding the clinical outcomes of fixed-dose irinotecan monotherapy for advanced gastric cancer: a multicenter retrospective study.
Thalassemia
Clinical Significance of UGT1A1 Genetic Analysis in Chinese Neonates with Severe Hyperbilirubinemia.
Thalassemia
Effects of variant UDP-glucuronosyltransferase 1A1 gene, glucose-6-phosphate dehydrogenase deficiency and thalassemia on cholelithiasis.
Thrombocytopenia
Effects of UGT1A1 genotype on the pharmacokinetics, pharmacodynamics, and toxicities of belinostat administered by 48-hour continuous infusion in patients with cancer.
Thrombocytopenia
Influence of UGT1A1 polymorphism on etoposide plus platinum-induced neutropenia in Japanese patients with small-cell lung cancer.
Thrombosis
Polymorphisms of CYP2C9, VKORC1, MDR1, APOE and UGT1A1 genes and the therapeutic warfarin dose in Brazilian patients with thrombosis: a prospective cohort study.
Thyroid Neoplasms
Effect of UGT1A1, UGT1A3, DIO1 and DIO2 polymorphisms on L-thyroxine doses required for TSH suppression in patients with differentiated thyroid cancer.
Triple Negative Breast Neoplasms
miR-452 Reverses Abnormal Glycosylation Modification of ER? and Estrogen Resistance in TNBC (Triple-Negative Breast Cancer) Through Targeting UGT1A1.
Tuberculosis
Effect of genetic variation in UGT1A and ABCB1 on moxifloxacin pharmacokinetics in South African patients with tuberculosis.
Urea Cycle Disorders, Inborn
Functional characterization of hepatocytes for cell transplantation: customized cell preparation for each receptor.
Urinary Bladder Neoplasms
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.
Urinary Bladder Neoplasms
An association of UDP-glucuronosyltransferase 2B7 C802T (His268Tyr) polymorphism with bladder cancer in benzidine-exposed workers in China.
Urinary Bladder Neoplasms
Association of genotypes of carcinogen-metabolizing enzymes and smoking status with bladder cancer in a Japanese population.
Urinary Bladder Neoplasms
Expression of UDP-glucuronosyltransferase 1A in bladder cancer: Association with prognosis and regulation by estrogen.
Urinary Bladder Neoplasms
Identification of low-frequency variants of UGT1A3 associated with bladder cancer risk by next-generation sequencing.
Urinary Bladder Neoplasms
Mapping of the UGT1A locus identifies an uncommon coding variant that affects mRNA expression and protects from bladder cancer.
Urinary Bladder Neoplasms
Occupational bladder cancer: Polymorphisms of xenobiotic metabolizing enzymes, exposures, and prognosis.
Urinary Bladder Neoplasms
Phase II Drug-Metabolizing Polymorphisms and Smoking Predict Recurrence of Non-Muscle-Invasive Bladder Cancer: A Gene-Smoking Interaction.
Urinary Bladder Neoplasms
Rs11892031[A] on chromosome 2q37 in an intronic region of the UGT1A locus is associated with urinary bladder cancer risk.
Urinary Bladder Neoplasms
Suppression of AhR signaling pathway is associated with the down-regulation of UDP-glucuronosyltransferases during BBN-induced urinary bladder carcinogenesis in mice.
Urinary Bladder Neoplasms
UDP-glucuronosyltransferase 2B7 C802T (His268Tyr) polymorphism in bladder cancer cases.
Urinary Bladder Neoplasms
[Association between genetic polymorphism of UGT1A7 and susceptibility of bladder cancer]
Urticaria
Polymorphisms of Aspirin-Metabolizing Enzymes CYP2C9, NAT2 and UGT1A6 in Aspirin-Intolerant Urticaria.
Uterine Cervical Neoplasms
UGT1A1 polymorphism has a prognostic effect in patients with stage IB or II uterine cervical cancer and one or no metastatic pelvic nodes receiving irinotecan chemotherapy: a retrospective study.
Uterine Cervical Neoplasms
[Study of irinotecan-induced toxicity and its correlation to UGT1A1 gene promoter polymorphisms].
Venous Thrombosis
Genetic variation in the first-pass metabolism of ethinylestradiol, sex hormone binding globulin levels and venous thrombosis risk.
Viremia
Significance of UGT1A1*28 Genotype in Patients with Advanced Liver Injury Caused By Chronic Hepatitis C.
Virus Diseases
UDP-glucuronosyltransferase 1A7 genetic polymorphisms are associated with hepatocellular carcinoma in japanese patients with hepatitis C virus infection.
Vitamin A Deficiency
Effect of vitamin A deficiency on pulmonary and hepatic in vitro metabolism of benzo(a)pyrene in rat.
Vitamin A Deficiency
Hepatic cytochrome P-450-dependent metabolism and enzymatic conjugation of foreign compounds in vitamin A-deficient rats.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
0.0073 - 0.072
(+-)-11-hydroxy-DELTA9-tetrahydrocannabinol
0.068 - 0.17
(-)-11-nor-9-carboxy-DELTA9-tetrahydrocannabinol
0.0062
(E)-2,4-dimethoxy-6-(4-methoxystyryl)benzaldehyde oxime
-
pH 7.4, 37°C
0.063 - 0.24
(E)-3-(3-hydroxy-4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)acrylic acid
-
pH 7.4, 37°C, isozyme-dependent
0.21
(R)-6-hydroxywarfarin
-
isoform UGT1A10, pH 7.6, 37°C
0.044 - 0.13
(R)-7-hydroxywarfarin
0.105
(R)-8-hydroxywarfarin
-
isoform UGT1A10, pH 7.6, 37°C
0.16 - 1.21
(R)-propanolol
0.36
(S)-6-hydroxywarfarin
-
isoform UGT1A10, pH 7.6, 37°C
0.16 - 0.23
(S)-7-hydroxywarfarin
0.139
(S)-8-hydroxywarfarin
-
isoform UGT1A10, pH 7.6, 37°C
0.507 - 1.013
(S)-naproxen
0.135 - 0.515
(S)-propanolol
0.247 - 0.263
1-hydroxy-benzo(a)pyrene
0.0061 - 0.011
1-hydroxy-benzo[a]pyrene
0.0012 - 0.0033
1-hydroxy-pyrene
0.0113 - 2.869
1-hydroxybenzo(a)pyrene
0.091 - 0.111
1-hydroxypyrene
0.0178 - 0.0353
10-gingerol
0.0069 - 0.093
11alpha-hydroxyprogesterone
0.073 - 0.211
16alpha-hydroxyprogesterone
0.042 - 0.159
17-epiestriol
0.00192 - 0.0975
17beta-estradiol
0.0073 - 0.0112
1alpha,25-dihydroxyvitamin D3
0.00298 - 0.0258
2',4,4'-trihydroxychalcone
0.00702 - 0.0804
2,3,4,5-Tetrachlorophenol
0.002 - 0.0648
2,3,4-Trichlorophenol
0.0322 - 0.06982
2,4,5-Trichlorophenol
0.01989 - 0.109
2,4,6-Trichlorophenol
0.05182 - 0.1542
2,4-Dichlorophenol
0.0119 - 0.293
2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid
0.1302
2-chlorophenol
pH 7.4, 37°C, recombinant UGT1A6, substrate inhibition model
0.014 - 0.027
2-hydroxyestradiol
0.0102 - 0.291
2-hydroxyestrone
0.551 - 13.4
3'-azido-3'-deoxythymidine
0.00347 - 0.0471
3,4,5-trichlorophenol
0.0738
3-chlorophenol
pH 7.4, 37°C, recombinant UGT1A6, substrate inhibition model
0.0444
3-epideacetycinobufagin
pH and temperature not specified in the publication
0.271 - 0.278
3-hydroxy-benzo(a)pyrene
0.0072 - 0.0075
3-hydroxy-benzo[a]pyrene
0.0097 - 0.583
3-hydroxybenzo(a)pyrene
0.00197 - 0.0047
3alpha,5beta-tetrahydroaldosterone
0.0588 - 0.286
4-aminobiphenyl
0.1286
4-Chlorophenol
pH 7.4, 37°C, recombinant UGT1A6, Michaelis-Menten model
0.006 - 0.292
4-hydroxyestradiol
0.014 - 0.1182
4-hydroxyestrone
0.011 - 1.621
4-methylumbeliferone
0.00012 - 4.204
4-Methylumbelliferone
0.0102 - 1.034
4-nitrophenol
0.0293 - 0.149
5-diethylaminoethylamino-8-hydroxyimidazoacridinone
0.0289 - 0.0706
5-dimethylaminopropylamino-8-hydroxytriazoloacridinone
0.135 - 3.674
5-hydroxytryptophol
0.124 - 1.25
5-methylchrysene-1,2-diol
0.016
5alpha-androstane-3alpha,17beta diol
apparent Km for UGT1A4
0.00023 - 0.00036
5alpha-dihydroaldosterone
0.0646 - 0.0647
5beta-tetrahydrocortisone
0.0253 - 0.404
6-gingerol
0.48 - 0.72
6-hydroxywarfarin
0.003 - 0.055
6alpha-hydroxyprogesterone
19.3 - 44.4
7-ethyl-10-hydroxycampothecin
0.0098 - 1.588
7-hydroxy benzo(a)pyrene
0.00418 - 0.198
7-hydroxy-4-trifluoromethylcoumarin
0.261 - 0.334
7-hydroxy-benzo(a)pyrene
0.0078 - 0.0085
7-hydroxy-benzo[a]pyrene
0.17 - 0.56
7-hydroxywarfarin
0.0132 - 0.0314
8-gingerol
0.308 - 0.368
8-hydroxy-benzo(a)pyrene
0.00048 - 0.494
8-hydroxyquinoline
0.19 - 0.39
8-hydroxywarfarin
0.0096 - 0.012
9-hydroxy-benzo[a]pyrene
0.0301 - 0.615
9-hydroxybenzo(a)pyrene
0.00036 - 0.00076
aldosterone
0.261
alprazolam
-
isoform UGT1A4, pH 7.4, 37°C
0.0075 - 0.49
amitriptyline
0.0175
androstanediol
-
pH 7.4, 37°C
0.0066 - 0.01
androsterone
0.0035 - 0.01005
bakuchiol
0.397 - 0.426
benzo(a)pyrene-7,8-diol
0.168 - 0.397
Benzo[a]pyrene-7,8-diol
0.12 - 0.19
benzo[a]pyrene-9,10-diol
0.021
beta-estradiol
-
isoform UGT1A1, pH 7.4, 37°C
0.028
bifonazole
-
isoform UGT1A4, pH 7.4, 37°C
0.0034 - 0.059
cannabinol
0.083
chenodeoxycholic acid
-
-
0.0074 - 0.193
cis-4-hydroxytamoxifen
0.4
codeine
-
isozyme UGT2B7, pH 7.5, 37°C
0.0278
cotinine
pH 7.4, 37°C, recombinant isozyme UGT2B10
0.086 - 0.228
cyproheptadine
3.133 - 7.724
desmethylnaproxen
0.284 - 0.307
dibenzo(a,l)pyrene-11,12-diol
0.096 - 0.143
dibenzo[a,1]pyrene-11,12-diol
0.0196
dihydrotestosterone
-
isoform UGT1A4, pH 7.4, 37°C
0.037 - 0.47
diphenhydramine
0.115
econazole
-
isoform UGT1A4, pH 7.4, 37°C
0.0017 - 0.0116
Epitestosterone
0.0049 - 0.0138
estradiol
1.667
fluconazole
-
isoform UGT2B7, pH 7.4, 37°C
0.0022 - 0.0195
gemfibrozil
0.011 - 0.27
hyodeoxycholic acid
0.0072 - 1.442
imipramine
0.007
ketoconazole
-
isoform UGT1A4, pH 7.4, 37°C
0.48
Ketoprofen
-
pH 7.4, 37°C
0.774 - 3.812
lamotrigine
0.059
miconazole
-
isoform UGT1A4, pH 7.4, 37°C
0.013
midazolam
-
isoform UGT1A4, pH 7.4, 37°C
0.019
Mn2+[side2]
37°C, pH 7.4
0.028 - 0.173
MOCAc-Lys-Arg-Gly-Leu-Tyr-Phe-Ile-Thr-His-Lys(Dnp)
0.012 - 0.081
montanoyl-CoA
1.15
morphine 3-glucuronide
-
pH 7.4, 37°C
0.046 - 0.336
Mycophenolic acid
0.135 - 7.344
niflumic acid
5.06 - 6.99
p-ethoxyphenylurea
0.00255
Pentachlorophenol
pH 7.4, 37°C, recombinant UGT1A1, substrate inhibition model
0.0198 - 0.1951
Phenylbutazone
0.0068 - 0.0964
phloretin
0.211 - 0.627
Protocatechuic aldehyde
0.51
senecionine
-
pH 7.4, 37°C
0.023
silybin A
at pH 7.4 and 37°C
0.0087
silybin B
at pH 7.4 and 37°C
0.009
silydianin
at pH 7.4 and 37°C
0.035
sulconazole
-
isoform UGT1A4, pH 7.4, 37°C
0.014 - 0.053
sulfinpyrazone
0.0009
tamoxifen
-
isoform UGT1A4, pH 7.4, 37°C
0.0038 - 0.0387
testosterone
0.00112
tetrahydrocurcumin
pH 7.4, 37°C
0.124
tioconazole
-
isoform UGT1A4, pH 7.4, 37°C
0.0056 - 0.0155
tizoxanide
0.0506 - 0.0515
tranilast
0.0037 - 0.319
trans-4-hydroxytamoxifen
0.008 - 0.255
trans-androsterone
0.013 - 0.135
trans-endoxifen
0.0197 - 0.305
Trifluoperazine
0.00025
UDP-D-glucuronate
pH 7.4, 37°C, recombinant wild-type isozyme UGT1A6
0.138 - 0.184
UDP-glucuronate
0.229 - 0.704
UDP-glucuronic acid
0.96
UDPglucuronic acid
-
-
0.111 - 0.339
umbelliferone
1.13
voriconazole
-
isoform UGT1A4, pH 7.4, 37°C
0.00579 - 0.4593
xanthotoxol
additional information
additional information
-
0.0073
(+-)-11-hydroxy-DELTA9-tetrahydrocannabinol

-
isoform UGT1A9, pH 7.4, 37°C
0.072
(+-)-11-hydroxy-DELTA9-tetrahydrocannabinol
-
isoform UGT1A10, pH 7.4, 37°C
0.068
(-)-11-nor-9-carboxy-DELTA9-tetrahydrocannabinol

-
isoform UGT1A3, pH 7.4, 37°C
0.17
(-)-11-nor-9-carboxy-DELTA9-tetrahydrocannabinol
-
isoform UGT1A1, pH 7.4, 37°C
0.044
(R)-7-hydroxywarfarin

-
isoform UGT1A10, pH 7.6, 37°C
0.13
(R)-7-hydroxywarfarin
-
isoform UGT1A1, pH 7.6, 37°C
0.16
(R)-propanolol

-
isoform UGT1A9, pH 7.4, 37°C
0.263
(R)-propanolol
-
isoform UGT2B7, pH 7.4, 37°C
1.21
(R)-propanolol
-
isoform UGT2B4, pH 7.4, 37°C
0.16
(S)-7-hydroxywarfarin

-
isoform UGT1A10, pH 7.6, 37°C
0.23
(S)-7-hydroxywarfarin
-
isoform UGT1A1, pH 7.6, 37°C
0.507
(S)-naproxen

-
mutant M33V, pH 7.4, 37°C
0.62
(S)-naproxen
-
mutant M33I, pH 7.4, 37°C
0.66
(S)-naproxen
-
mutant M33Q, pH 7.4, 37°C
0.79
(S)-naproxen
-
wildtype, pH 7.4, 37°C
1.013
(S)-naproxen
-
mutant M33T, pH 7.4, 37°C
0.135
(S)-propanolol

-
isoform UGT1A9, pH 7.4, 37°C
0.289
(S)-propanolol
-
isoform UGT2B7, pH 7.4, 37°C
0.515
(S)-propanolol
-
isoform UGT2B4, pH 7.4, 37°C
0.247
1-hydroxy-benzo(a)pyrene

-
wild-type, pH 7.4, 37°C
0.263
1-hydroxy-benzo(a)pyrene
-
mutant K75R, pH 7.4, 37°C
0.0061
1-hydroxy-benzo[a]pyrene

with UDP-D-xylose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.011
1-hydroxy-benzo[a]pyrene
with UDP-D-glucose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.0012
1-hydroxy-pyrene

with UDP-D-xylose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.0033
1-hydroxy-pyrene
with UDP-D-glucose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.0113
1-hydroxybenzo(a)pyrene

37°C, pH 7.5
0.0299
1-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.0342
1-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.087
1-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.0963
1-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.169
1-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.854
1-hydroxybenzo(a)pyrene
37°C, pH 7.5
1.526
1-hydroxybenzo(a)pyrene
37°C, pH 7.5
2.869
1-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.091
1-hydroxypyrene

-
wild-type, pH 7.4, 37°C
0.111
1-hydroxypyrene
-
mutant K75R, pH 7.4, 37°C
0.03
1-naphthol

-
wild-type, pH 7.4, 37°C
0.044
1-naphthol
-
mutant K75R, pH 7.4, 37°C
0.048
1-naphthol
-
H379A mutant isozyme UGT1A6
0.083
1-naphthol
-
H371A mutant isozyme UGT1A6
0.084
1-naphthol
-
isoform UGT1A6, pH 7.4, 37°C
0.129
1-naphthol
with UDP-D-xylose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.225
1-naphthol
with UDP-D-glucose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.265
1-naphthol
-
pH 7.4, 37°C
27
1-naphthol
-
wild-type isozyme UGT1A6
0.0178
10-gingerol

P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT1A9
0.0224
10-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT2B7
0.0308
10-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT1A1
0.0313
10-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT2B17
0.033
10-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT1A8
0.0353
10-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT1A8
0.0069
11alpha-hydroxyprogesterone

37°C, pH 7.4
0.093
11alpha-hydroxyprogesterone
37°C, pH 7.4
0.073
16alpha-hydroxyprogesterone

37°C, pH 7.4
0.211
16alpha-hydroxyprogesterone
37°C, pH 7.4
0.042
17-epiestriol

native UGT2B4
0.052
17-epiestriol
native UGT2B4
0.063
17-epiestriol
mutant UGT2B4(Y33L)
0.071
17-epiestriol
mutant UGT2B4(F33Y)
0.093
17-epiestriol
mutant UGT2B4(F33L)
0.159
17-epiestriol
mutant UGT2B4(Y33F)
0.00192
17beta-estradiol

recombinant mutant M59I, pH 7.5, 37°C
0.00233
17beta-estradiol
recombinant mutant T202I, pH 7.5, 37°C
0.00234
17beta-estradiol
recombinant wild-type enzyme, pH 7.5, 37°C
0.0143
17beta-estradiol
-
isoform UGT1A10, pH 7.4, 37°C
0.0297
17beta-estradiol
-
isoform UGT2B7, pH 7.4, 37°C
0.0975
17beta-estradiol
-
isoform UGT2A1, pH 7.4, 37°C
0.0073
1alpha,25-dihydroxyvitamin D3

25-O-glucuronidation of 1alpha,25-dihydroxyvitamin D3 by UGT1A4 supersomes
0.0112
1alpha,25-dihydroxyvitamin D3
25-O-glucuronidation of 1alpha,25-dihydroxyvitamin D3 by liver microsomes
0.00298
2',4,4'-trihydroxychalcone

-
isoform UGT1A1, product 2',4,4'-trihydroxychalcone 2'-O-glucoside
0.00315
2',4,4'-trihydroxychalcone
-
isoform UGT1A9, product 2',4,4'-trihydroxychalcone 4'-O-glucoside
0.0043
2',4,4'-trihydroxychalcone
-
isoform UGT1A1, product 2',4,4'-trihydroxychalcone 4'-O-glucoside
0.0258
2',4,4'-trihydroxychalcone
-
isoform UGT1A10, product 2',4,4'-trihydroxychalcone 2'-O-glucoside
0.00702
2,3,4,5-Tetrachlorophenol

pH 7.4, 37°C, recombinant UGT1A8, substrate inhibition model
0.0804
2,3,4,5-Tetrachlorophenol
pH 7.4, 37°C, recombinant UGT1A1, substrate inhibition model
0.002
2,3,4-Trichlorophenol

pH 7.4, 37°C, recombinant UGT1A6, substrate inhibition model
0.0269
2,3,4-Trichlorophenol
pH 7.4, 37°C, recombinant UGT1A8, substrate inhibition model
0.04554
2,3,4-Trichlorophenol
pH 7.4, 37°C, recombinant UGT1A10, substrate inhibition model
0.0648
2,3,4-Trichlorophenol
pH 7.4, 37°C, recombinant UGT1A1, substrate inhibition model
0.0322
2,4,5-Trichlorophenol

pH 7.4, 37°C, recombinant UGT1A8, substrate inhibition model
0.06982
2,4,5-Trichlorophenol
pH 7.4, 37°C, recombinant UGT1A6, substrate inhibition model
0.01989
2,4,6-Trichlorophenol

pH 7.4, 37°C, recombinant UGT1A6, substrate inhibition model
0.109
2,4,6-Trichlorophenol
pH 7.4, 37°C, recombinant UGT1A8, substrate inhibition model
0.05182
2,4-Dichlorophenol

pH 7.4, 37°C, recombinant UGT1A6, substrate inhibition model
0.1542
2,4-Dichlorophenol
pH 7.4, 37°C, recombinant UGT1A8, substrate inhibition model
0.0119
2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid

Hill equation
0.0456
2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid
Hill equation
0.138
2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid
-
0.293
2-(4-chlorophenyl)-5-(2-furyl)-4-oxazoleacetic acid
Hill equation
0.014
2-hydroxyestradiol

-
apparent Km on expressed UGT2B7Y, 2 mM UDP glucuronic acid
0.024
2-hydroxyestradiol
apparent Km for UGT1A3
0.025
2-hydroxyestradiol
apparent Km for UGT1A1
0.026
2-hydroxyestradiol
-
apparent Km on expressed UGT1A3, 2 mM UDP glucuronic acid
0.027
2-hydroxyestradiol
-
apparent Km on expressed UGT1A1, 2 mM UDP glucuronic acid
0.0102
2-hydroxyestrone

37°C, pH 8.0, mutant enzyme F93A
0.021
2-hydroxyestrone
apparent Km for UGT1A3
0.024
2-hydroxyestrone
-
apparent Km on expressed UGT1A3, 2 mM UDP glucuronic acid
0.024
2-hydroxyestrone
apparent Km for UGT1A1
0.026
2-hydroxyestrone
-
apparent Km on expressed UGT1A1, 2 mM UDP glucuronic acid
0.066
2-hydroxyestrone
-
apparent Km on expressed UGT2B7Y, 2 mM UDP glucuronic acid
0.0823
2-hydroxyestrone
37°C, pH 8.0, mutant enzyme F93L
0.1305
2-hydroxyestrone
37°C, pH 8.0, wild-type enzyme
0.291
2-hydroxyestrone
37°C, pH 8.0, mutant enzyme F90L
0.551
3'-azido-3'-deoxythymidine

pH 7.4, 37°C
0.77
3'-azido-3'-deoxythymidine
-
isozyme UGT2B7, pH 7.5, 37°C
13.4
3'-azido-3'-deoxythymidine
-
-
0.00347
3,4,5-trichlorophenol

pH 7.4, 37°C, recombinant UGT1A6, substrate inhibition model
0.0471
3,4,5-trichlorophenol
pH 7.4, 37°C, recombinant UGT1A8, substrate inhibition model
0.271
3-hydroxy-benzo(a)pyrene

-
wild-type, pH 7.4, 37°C
0.278
3-hydroxy-benzo(a)pyrene
-
mutant K75R, pH 7.4, 37°C
0.0072
3-hydroxy-benzo[a]pyrene

with UDP-D-xylose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.0075
3-hydroxy-benzo[a]pyrene
with UDP-D-glucose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.0097
3-hydroxybenzo(a)pyrene

37°C, pH 7.5
0.0556
3-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.0635
3-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.115
3-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.234
3-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.295
3-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.348
3-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.497
3-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.583
3-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.00197
3alpha,5beta-tetrahydroaldosterone

isozyme UGT2B7Y268, pH 7.5, 37°C
0.0047
3alpha,5beta-tetrahydroaldosterone
isozyme UGT2B7H268, pH 7.5, 37°C
0.0588
4-aminobiphenyl

-
0.251
4-aminobiphenyl
-
mutant D148A
0.269
4-aminobiphenyl
-
wild-type
0.286
4-aminobiphenyl
-
mutant H37A
0.006
4-hydroxyestradiol

-
apparent Km on expressed UGT1A1, 2 mM UDP glucuronic acid
0.007
4-hydroxyestradiol
-
apparent Km on expressed UGT2B7Y, 2 mM UDP glucuronic acid
0.01
4-hydroxyestradiol
apparent Km for UGT2B7
0.038
4-hydroxyestradiol
-
apparent Km on expressed UGT1A3, 2 mM UDP glucuronic acid
0.0401
4-hydroxyestradiol
37°C, pH 8.0, mutant enzyme F93A
0.2338
4-hydroxyestradiol
37°C, pH 8.0, wild-type enzyme
0.292
4-hydroxyestradiol
37°C, pH 8.0, mutant enzyme F90L
0.014
4-hydroxyestrone

apparent Km for UGT2B7
0.016
4-hydroxyestrone
-
apparent Km on expressed UGT2B7Y, 2 mM UDP glucuronic acid
0.019
4-hydroxyestrone
-
apparent Km on expressed UGT1A1, 2 mM UDP glucuronic acid
0.0401
4-hydroxyestrone
37°C, pH 8.0, mutant enzyme F93A
0.053
4-hydroxyestrone
-
apparent Km on expressed UGT1A3, 2 mM UDP glucuronic acid
0.1182
4-hydroxyestrone
37°C, pH 8.0, wild-type enzyme
0.011
4-methylumbeliferone

-
wildtype, pH 7.4, 37°C
0.228
4-methylumbeliferone
-
mutant M33Q, pH 7.4, 37°C
0.233
4-methylumbeliferone
-
mutant M33I, pH 7.4, 37°C
0.234
4-methylumbeliferone
-
mutant M33V, pH 7.4, 37°C
1.621
4-methylumbeliferone
-
mutant M33T, pH 7.4, 37°C
0.00012
4-Methylumbelliferone

pH 7.4, 37°C, recombinant wild-type isozyme UGT1A6
0.0021
4-Methylumbelliferone
mutant L173A, pH 7.4, 37°C
0.0029
4-Methylumbelliferone
pH 7.4, 37°C, isozyme UGT1A9 in presence of 2% fatty acid-free human serum albumin
0.0036
4-Methylumbelliferone
mutant K91M/A92D, pH 7.4, 37°C
0.0044
4-Methylumbelliferone
wild-type, pH 7.4, 37°C
0.0044
4-Methylumbelliferone
mutant E241A, pH 7.4, 37°C
0.0056
4-Methylumbelliferone
mutant Y106F/G111S/D115G, pH 7.4, 37°C
0.0059
4-Methylumbelliferone
mutant L219F/H221Q/R222Y, pH 7.4, 37°C
0.008
4-Methylumbelliferone
isozyme UGT1A9, pH 7.4, 37°C
0.009
4-Methylumbelliferone
isozyme UGT1A6, Michaelis-Menten kinetic, pH 7.4, 37°C
0.0091
4-Methylumbelliferone
mutant N152A, pH 7.4, 37°C
0.0101
4-Methylumbelliferone
mutant R42Q, pH 7.4, 37°C
0.0134
4-Methylumbelliferone
pH 7.4, 37°C, isozyme UGT1A9
0.014
4-Methylumbelliferone
isozyme UGT1A7, Michaelis-Menten kinetic, pH 7.4, 37°C
0.015
4-Methylumbelliferone
-
mutant D143A
0.021
4-Methylumbelliferone
-
wild-type
0.031
4-Methylumbelliferone
isozyme UGT1A10, Michaelis-Menten kinetic, pH 7.4, 37°C
0.0522
4-Methylumbelliferone
37°C, pH 7.4
0.054
4-Methylumbelliferone
pH 7.5, 37°C, 0.2 mM propofol, isozyme UGT1A1
0.0766
4-Methylumbelliferone
37°C, pH 7.4
0.0924
4-Methylumbelliferone
37°C, pH 7.4
0.101
4-Methylumbelliferone
pH 7.5, 37°C, isozyme UGT1A1
0.108
4-Methylumbelliferone
37°C, pH 7.4
0.113
4-Methylumbelliferone
isozyme UGT1A1, Michaelis-Menten kinetic, pH 7.4, 37°C
0.115
4-Methylumbelliferone
isozyme UGT1A1, pH 7.4, 37°C
0.1226
4-Methylumbelliferone
37°C
0.149
4-Methylumbelliferone
isozyme UGT2B15, pH 7.4, 37°C
0.157
4-Methylumbelliferone
isozyme UGT1A6, pH 7.4, 37°C
0.17
4-Methylumbelliferone
-
wild-type isozyme UGT1A6
0.18
4-Methylumbelliferone
isozyme UGT1A9, pH 7.4, 37°C
0.1917
4-Methylumbelliferone
isoform UGT1A8, pH 7.4, 37°C
0.2376
4-Methylumbelliferone
37°C, pH 7.4
0.253
4-Methylumbelliferone
isozyme UGT2B15, pH 7.4, 37°C
0.335
4-Methylumbelliferone
isozyme UGT2B7, Hill equation, pH 7.4, 37°C
0.335
4-Methylumbelliferone
isozyme UGT1A3, pH 7.4, 37°C
0.58
4-Methylumbelliferone
-
H379A mutant isozyme UGT1A6
0.66
4-Methylumbelliferone
-
H371A mutant isozyme UGT1A6
0.73
4-Methylumbelliferone
isozyme UGT1A8, pH 7.4, 37°C
0.967
4-Methylumbelliferone
-
mutant D148A
1.159
4-Methylumbelliferone
isozyme UGT1A3, pH 7.4, 37°C
4.204
4-Methylumbelliferone
isozyme UGT2B17, pH 7.4, 37°C
0.0102
4-nitrophenol

mutant Y106F/G111S/D115G, pH 7.4, 37°C
0.0152
4-nitrophenol
mutant L219F/H221Q/R222Y, pH 7.4, 37°C
0.0157
4-nitrophenol
mutant L173A, pH 7.4, 37°C
0.0169
4-nitrophenol
wild-type, pH 7.4, 37°C
0.0178
4-nitrophenol
mutant K91M/A92D, pH 7.4, 37°C
0.0188
4-nitrophenol
mutant E241A, pH 7.4, 37°C
0.03
4-nitrophenol
mutant R42Q, pH 7.4, 37°C
0.0492
4-nitrophenol
mutant N152A, pH 7.4, 37°C
0.0496
4-nitrophenol
37°C, pH 7.4
0.1508
4-nitrophenol
37°C, pH 7.4
0.3359
4-nitrophenol
37°C, pH 7.4
0.5191
4-nitrophenol
37°C, pH 7.4
0.73
4-nitrophenol
-
pH 7.5, 37°C, genetic variant UGT1A6*1, co-expression of splice variants i1 and i2
0.77
4-nitrophenol
-
pH 7.5, 37°C, genetic variant UGT1A6*1
0.803
4-nitrophenol
37°C, pH 7.4
1.034
4-nitrophenol
37°C, pH 7.4
0.0293
5-diethylaminoethylamino-8-hydroxyimidazoacridinone

-
isoform UGT1A7, pH not specified in the publication, temperature not specified in the publication
0.0546
5-diethylaminoethylamino-8-hydroxyimidazoacridinone
-
isoform UGT1A9, pH not specified in the publication, temperature not specified in the publication
0.094
5-diethylaminoethylamino-8-hydroxyimidazoacridinone
-
isoform UGT1A10, pH not specified in the publication, temperature not specified in the publication
0.149
5-diethylaminoethylamino-8-hydroxyimidazoacridinone
-
isoform UGT1A1, pH not specified in the publication, temperature not specified in the publication
0.0289
5-dimethylaminopropylamino-8-hydroxytriazoloacridinone

-
isoform UGT1A1, pH not specified in the publication, temperature not specified in the publication
0.0633
5-dimethylaminopropylamino-8-hydroxytriazoloacridinone
-
isoform UGT1A9, pH not specified in the publication, temperature not specified in the publication
0.0706
5-dimethylaminopropylamino-8-hydroxytriazoloacridinone
-
isoform UGT1A10, pH not specified in the publication, temperature not specified in the publication
0.135
5-hydroxytryptophol

isozyme UGT1A6, pH 7.5, 37°C
3.674
5-hydroxytryptophol
isozyme UGT1A9, pH 7.5, 37°C
0.124
5-methylchrysene-1,2-diol

with UDP-D-xylose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.27
5-methylchrysene-1,2-diol
-
wild-type, pH 7.4, 37°C
0.381
5-methylchrysene-1,2-diol
-
mutant K75R, pH 7.4, 37°C
1.25
5-methylchrysene-1,2-diol
with UDP-D-glucose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.00023
5alpha-dihydroaldosterone

isozyme UGT2B7H268, pH 7.5, 37°C
0.00036
5alpha-dihydroaldosterone
isozyme UGT2B7Y268, pH 7.5, 37°C
0.0646
5beta-tetrahydrocortisone

isozyme UGT2B7H268, pH 7.5, 37°C
0.0647
5beta-tetrahydrocortisone
isozyme UGT2B7Y268, pH 7.5, 37°C
0.0253
6-gingerol

P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT2B15
0.0488
6-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT2B17
0.0543
6-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT1A8
0.138
6-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT1A8
0.158
6-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT1A9
0.206
6-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT1A10
0.232
6-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT1A1
0.404
6-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT2B7
0.48
6-hydroxywarfarin

-
wild-type, pH 7.4, 37°C
0.7
6-hydroxywarfarin
-
mutant V92A, pH 7.4, 37°C
0.72
6-hydroxywarfarin
-
mutant F93A, pH 7.4, 37°C
0.003
6alpha-hydroxyprogesterone

37°C, pH 7.4
0.055
6alpha-hydroxyprogesterone
37°C, pH 7.4
19.3
7-ethyl-10-hydroxycampothecin

recombinant wild-type isozyme UGT1A9, pH.4, 37°C
44.4
7-ethyl-10-hydroxycampothecin
recombinant UGT1A9 mutant D256N isozyme, pH.4, 37°C
0.0098
7-hydroxy benzo(a)pyrene

37°C, pH 7.5
0.0501
7-hydroxy benzo(a)pyrene
37°C, pH 7.5
0.0621
7-hydroxy benzo(a)pyrene
37°C, pH 7.5
0.127
7-hydroxy benzo(a)pyrene
37°C, pH 7.5
0.129
7-hydroxy benzo(a)pyrene
37°C, pH 7.5
0.19
7-hydroxy benzo(a)pyrene
37°C, pH 7.5
0.281
7-hydroxy benzo(a)pyrene
37°C, pH 7.5
0.542
7-hydroxy benzo(a)pyrene
37°C, pH 7.5
1.588
7-hydroxy benzo(a)pyrene
37°C, pH 7.5
0.00418
7-hydroxy-4-trifluoromethylcoumarin

recombinant mutant M59I, pH 7.5, 37°C
0.00491
7-hydroxy-4-trifluoromethylcoumarin
recombinant wild-type enzyme, pH 7.5, 37°C
0.00537
7-hydroxy-4-trifluoromethylcoumarin
recombinant mutant T202I, pH 7.5, 37°C
0.198
7-hydroxy-4-trifluoromethylcoumarin
recombinant isoform UGT1A1, pH 7.4, 37°C
0.261
7-hydroxy-benzo(a)pyrene

-
wild-type, pH 7.4, 37°C
0.334
7-hydroxy-benzo(a)pyrene
-
mutant K75R, pH 7.4, 37°C
0.0078
7-hydroxy-benzo[a]pyrene

with UDP-D-glucose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.0085
7-hydroxy-benzo[a]pyrene
with UDP-D-xylose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.17
7-hydroxywarfarin

-
wild-type, pH 7.4, 37°C
0.56
7-hydroxywarfarin
-
mutant V92A, pH 7.4, 37°C
0.0132
8-gingerol

P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT1A9
0.0211
8-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT2B17
0.0235
8-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT2B7
0.0293
8-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT1A1
0.0314
8-gingerol
P16662, P19224, O60656, P22309, P22310, Q9HAW7, Q9HAW9, P35503, Q9HAW8, P54855, O75795, P06133 pH 7.4, temperature not specified in the publication, isozyme UGT1A8
0.308
8-hydroxy-benzo(a)pyrene

-
wild-type, pH 7.4, 37°C
0.368
8-hydroxy-benzo(a)pyrene
-
mutant K75R, pH 7.4, 37°C
0.00048
8-hydroxyquinoline

isozyme UGT1A9, pH 7.4, 37°C
0.0065
8-hydroxyquinoline
isozyme UGT1A6, pH 7.4, 37°C
0.016
8-hydroxyquinoline
isozyme UGT2B15, pH 7.4, 37°C
0.301
8-hydroxyquinoline
isozyme UGT2B7, pH 7.4, 37°C
0.494
8-hydroxyquinoline
isozyme UGT1A3, pH 7.4, 37°C
0.19
8-hydroxywarfarin

-
mutant F90A, pH 7.4, 37°C
0.304
8-hydroxywarfarin
-
mutant F93A, pH 7.4, 37°C
0.39
8-hydroxywarfarin
-
wild-type, pH 7.4, 37°C
0.39
8-hydroxywarfarin
-
mutant V92A, pH 7.4, 37°C
0.0096
9-hydroxy-benzo[a]pyrene

with UDP-D-xylose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.012
9-hydroxy-benzo[a]pyrene
with UDP-D-glucose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.0301
9-hydroxybenzo(a)pyrene

37°C, pH 7.5
0.0382
9-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.0633
9-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.0918
9-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.125
9-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.208
9-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.209
9-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.481
9-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.615
9-hydroxybenzo(a)pyrene
37°C, pH 7.5
0.00036
aldosterone

isozyme UGT2B7Y268, pH 7.5, 37°C
0.00076
aldosterone
isozyme UGT2B7H268, pH 7.5, 37°C
0.0075
amitriptyline

pH 7.4, 37°C
0.45
amitriptyline
pH 7.4, 37°C
0.49
amitriptyline
pH 7.4, 37°C
0.0066
androsterone

apparent Km for UGT2B7
0.01
androsterone
apparent Km for UGT2B7(H)
0.01
anthraflavic acid

isozyme UGT1A9, pH 7.6, 37°C
0.01
anthraflavic acid
isozyme UGT1A1, pH 6.4 or pH 7.6, 37°C
0.0035
bakuchiol

isoform UGT2B15, at pH 7.4 and 37°C
0.00441
bakuchiol
isoform Ugt1a1, at pH 7.4 and 37°C
0.01005
bakuchiol
isoform UGT1A3, at pH 7.4 and 37°C
0.397
benzo(a)pyrene-7,8-diol

-
wild-type, pH 7.4, 37°C
0.426
benzo(a)pyrene-7,8-diol
-
mutant K75R, pH 7.4, 37°C
0.168
Benzo[a]pyrene-7,8-diol

with UDP-D-xylose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.397
Benzo[a]pyrene-7,8-diol
with UDP-D-glucose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.12
benzo[a]pyrene-9,10-diol

with UDP-D-xylose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.19
benzo[a]pyrene-9,10-diol
with UDP-D-glucose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.004
bilirubin

-
pH 7.5, 37°C, recombinant UGT1A1
0.0062
bilirubin
-
pH 7.5, 37°C, liver UGT1A1
0.014
bilirubin
-
apparent Km for UGT1.1
0.024
bilirubin
apparent Km for UGT1A1
0.0034
cannabinol

-
isoform UGT1A9, pH 7.4, 37°C
0.019
cannabinol
-
isoform UGT1A7, pH 7.4, 37°C
0.044
cannabinol
-
isoform UGT1A8, pH 7.4, 37°C
0.059
cannabinol
-
isoform UGT1A10, pH 7.4, 37°C
0.071
carvacrol

-
isoform UGT1A3, pH 7.4, 37°C
0.078
carvacrol
-
isoform UGT1A9, pH 7.4, 37°C
0.14
carvacrol
-
isoform UGT1A6, pH 7.4, 37°C
0.282
carvacrol
-
isoform UGT1A7, pH 7.4, 37°C
0.368
carvacrol
-
isoform UGT2B7, pH 7.4, 37°C
0.004
chrysin

isozyme UGT1A1, pH 7.6, 37°C
0.005
chrysin
isozyme UGT1A1, pH 6.4, 37°C
0.0074
cis-4-hydroxytamoxifen

pH 7.4, 37°C, isozyme UGT1A7
0.015
cis-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT2B7
0.018
cis-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT2B17
0.02
cis-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT2B15
0.03
cis-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT1A10
0.041
cis-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT2B17
0.056
cis-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT1A8
0.07
cis-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT1A9
0.165
cis-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT1A3
0.193
cis-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT1A1
0.025
clozapine

recombinant mutant isozyme UGT1A4 L48V, pH 8.4, 37°C
0.049
clozapine
recombinant wild-type isozyme UGT1A4, pH 8.4, 37°C
0.00168
curcumin

pH 7.4, 37°C
0.1
curcumin
isozyme UGT1A7, pH 7.6, 37°C
0.1
curcumin
isozyme UGT1A8, pH 7.0, 37°C
0.1
curcumin
isozyme UGT1A1, pH 6.4, 37°C
0.1
curcumin
isozymes UGT1A1 and UGT1A10, pH 6.4, 37°C
0.086
cyproheptadine

recombinant mutant isozyme UGT1A4 L48V, pH 8.4, 37°C
0.228
cyproheptadine
recombinant wild-type isozyme UGT1A4, pH 8.4, 37°C
7.4
deferiprone

-
pH 7.5, 37°C, genetic variant UGT1A6*3
8.2
deferiprone
-
pH 7.5, 37°C, genetic variant UGT1A6*2
8.2
deferiprone
-
pH 7.5, 37°C, genetic variant UGT1A6*4
8.2
deferiprone
-
pH 7.5, 37°C, genetic variant UGT1A6*5
10
deferiprone
-
pH 7.5, 37°C, genetic variant UGT1A6*1
19.3
deferiprone
-
pH 7.5, 37°C, genetic variant UGT1A6*1, co-expression of splice variants i1 and i2
1.48
denopamine

recombinant isozyme UGT2B7, substrate denopamine, pH 7.5, 37°C
2.87
denopamine
liver micosomes, substrate denopamine, pH 7.5, 37°C
2.99
denopamine
jejunum microsomes, substrate denopamine, pH 7.5, 37°C
3.133
desmethylnaproxen

37°C, pH 7.4
3.384
desmethylnaproxen
37°C, pH 7.4
7.724
desmethylnaproxen
37°C, pH 7.4
0.284
dibenzo(a,l)pyrene-11,12-diol

-
wild-type, pH 7.4, 37°C
0.307
dibenzo(a,l)pyrene-11,12-diol
-
mutant K75R, pH 7.4, 37°C
0.096
dibenzo[a,1]pyrene-11,12-diol

with UDP-D-glucose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.143
dibenzo[a,1]pyrene-11,12-diol
with UDP-D-xylose, recombinant enzyme in microsomes, pH 7.4, 37°C
0.013
diclofenac

-
UGT2B7
0.016
diclofenac
-
UGT1A9
0.02
diclofenac
-
liver microsomes
0.056
diclofenac
-
isoform UGT2B10, pH 7.4, 37°C
0.069
diclofenac
-
isoform UGT2B7, pH 7.4, 37°C
0.037
diphenhydramine

pH 7.4, 37°C
0.47
diphenhydramine
pH 7.4, 37°C
1.89
dopamine

-
formation of dopamine-4-O-glucuronide, mutant F90A
1.95
dopamine
-
formation of dopamine-4-O-glucuronide, wild-type
1.99
dopamine
-
formation of dopamine-3-O-glucuronide, mutant F90A
2.19
dopamine
-
formation of dopamine-3-O-glucuronide, wild-type
2.31
dopamine
-
formation of dopamine-3-O-glucuronide, mutant F90L
2.59
dopamine
-
formation of dopamine-4-O-glucuronide, mutant F90L
2.63
dopamine
-
formation of dopamine-4-O-glucuronide, mutant F93A
2.67
dopamine
-
formation of dopamine-3-O-glucuronide, mutant F93L
2.91
dopamine
-
formation of dopamine-3-O-glucuronide, mutant F93A
3.11
dopamine
-
formation of dopamine-4-O-glucuronide, mutant F93L
0.021
entacapone

isozyme UGT1A9, pH 7.4, 37°C
0.0457
entacapone
-
membrane-bound recombinant isoform UGT1A10 from CHO cells, at pH 7.4 and 37°C
0.0569
entacapone
-
membrane-bound recombinant isoform UGT1A10 from HEK-293 cells, at pH 7.4 and 37°C
0.294
entacapone
isozyme UGT1A3, pH 7.4, 37°C
0.554
entacapone
-
with phospholipid purified recombinant isoform UGT1A10 from CHO cells, at pH 7.4 and 37°C
0.703
entacapone
-
without phospholipid purified recombinant isoform UGT1A10 from CHO cells, at pH 7.4 and 37°C
0.0017
Epitestosterone

-
isoform UGT2B7, pH 7.4, 37°C
0.0116
Epitestosterone
-
isoform UGT2A1, pH 7.4, 37°C
0.0049
estradiol

37°C, pH 8.0, mutant enzyme F90L
0.0078
estradiol
37°C, pH 8.0, mutant enzyme F93A
0.0138
estradiol
37°C, pH 8.0, wild-type enzyme
0.0388
estriol

37°C, pH 8.0, wild-type enzyme
0.0467
estriol
37°C, pH 8.0, mutant enzyme F93A
0.0063
estrone

37°C, pH 8.0, mutant enzyme F93A
0.0421
estrone
37°C, pH 8.0, wild-type enzyme
8.03
ethanol

pH 7.4, 37°C, enzyme UGT2B15
10.33
ethanol
pH 7.4, 37°C, enzyme UGT1A1
12.05
ethanol
pH 7.4, 37°C, enzyme UGT1A4
21.46
ethanol
pH 7.4, 37°C, enzyme UGT1A6
26.17
ethanol
pH 7.4, 37°C, enzyme UGT1A9
32.41
ethanol
pH 7.4, 37°C, enzyme UGT2B7
35.07
ethanol
pH 7.4, 37°C, enzyme UGT2B10
40.04
ethanol
pH 7.4, 37°C, enzyme UGT1A3
0.44
etoposide

liver microsomes, pH 7.4, 37°C
0.5
etoposide
recombinant isozyme UGT1A1, pH 7.4, 37°C
0.0084
eugenol

isozyme UGT1A10, pH 7.6, 37°C
0.0159
eugenol
isozyme UGT1A7, pH 6.4, 37°C
0.0245
eugenol
isozyme UGT1A10, pH 6.4, 37°C
0.0257
eugenol
isozyme UGT1A7, pH 8.5, 37°C
0.0209
frusemide

-
mutant M33T, pH 7.4, 37°C
0.129
frusemide
-
mutant M33V, pH 7.4, 37°C
0.183
frusemide
-
mutant M33Q, pH 7.4, 37°C
0.187
frusemide
-
mutant M33I, pH 7.4, 37°C
0.229
frusemide
-
wildtype, pH 7.4, 37°C
0.0022
gemfibrozil

-
pH 7.5, 37°C, isozyme UGT2B7
0.0195
gemfibrozil
-
pH 7.4, 37°C
2.1
grepafloxacin

isozyme UGT1A9, pH 7.4, 37°C
2.7
grepafloxacin
isozyme UGT1A1, pH 7.4, 37°C
5.2
grepafloxacin
liver microsomes, pH 7.4, 37°C
0.011
hyodeoxycholic acid

apparent Km for UGT2B7(H)
0.021
hyodeoxycholic acid
native UGT2B4
0.025
hyodeoxycholic acid
native UGT2B4
0.029
hyodeoxycholic acid
mutant UGT2B4(Y33L)
0.039
hyodeoxycholic acid
mutant UGT2B4(Y33F)
0.044
hyodeoxycholic acid
recombinant genetic variant UGT2A3.2
0.069
hyodeoxycholic acid
recombinant genetic variant UGT2A3.1
0.091
hyodeoxycholic acid
mutant UGT2B4(F33Y)
0.27
hyodeoxycholic acid
apparent Km for UGT2B4
0.0072
imipramine

pH 7.4, 37°C
0.071
imipramine
-
UGT1A4 expressed on B lymphoblastoid cells
0.097
imipramine
-
high affinity component from liver microsomes
0.276
imipramine
recombinant mutant isozyme UGT1A4 L48V, pH 8.4, 37°C
0.5
imipramine
pH 7.4, 37°C
0.7
imipramine
-
low affinity component from liver microsomes
0.76
imipramine
pH 7.4, 37°C
1.1
imipramine
imipramine N-glucuronide formation
1.4
imipramine
imipramine N-glucuronide formation, 1A4 co-expressed with isoform 1A4
1.4
imipramine
imipramine N-glucuronide formation, 1A4 co-expressed with isoform 1A6
1.442
imipramine
recombinant wild-type isozyme UGT1A4, pH 8.4, 37°C
0.368
labetalol

pH 7.5, 37°C, recombinant isozyme UGT1A9
0.386
labetalol
pH 7.5, 37°C, recombinant isozyme UGT2B7
0.956
labetalol
pH 7.5, 37°C, recombinant isozyme UGT1A1
0.774
lamotrigine

-
isoform UGT1A1 mutant H39P
1.564
lamotrigine
-
isoform UGT1A4, pH 7.4, 37°C
1.579
lamotrigine
-
isoform UGT1A4
3.812
lamotrigine
-
isoform UGT1A9 mutant H37P
2.6
levofloxacin

isozyme UGT1A9, pH 7.4, 37°C
6
levofloxacin
isozyme UGT1A1, pH 7.4, 37°C
10
levofloxacin
liver microsomes, pH 7.4, 37°C
0.028
MOCAc-Lys-Arg-Gly-Leu-Tyr-Phe-Ile-Thr-His-Lys(Dnp)

native UGT2B4
0.117
MOCAc-Lys-Arg-Gly-Leu-Tyr-Phe-Ile-Thr-His-Lys(Dnp)
mutant UGT2B4(Y33F)
0.131
MOCAc-Lys-Arg-Gly-Leu-Tyr-Phe-Ile-Thr-His-Lys(Dnp)
mutant UGT2B4(F33Y)
0.173
MOCAc-Lys-Arg-Gly-Leu-Tyr-Phe-Ile-Thr-His-Lys(Dnp)
mutant UGT2B4(F33L)
0.012
montanoyl-CoA

mutant UGT2B4(Y33L)
0.081
montanoyl-CoA
native UGT2B4
0.0355
morphine

pH 7.5, 37°C, isozyme UGT1A8, at 0.05 mM morphine
0.0404
morphine
pH 7.5, 37°C, isozyme UGT1A1, at 0.05 mM morphine
0.0679
morphine
pH 7.5, 37°C, isozyme UGT1A1, at 2.5 mM morphine
0.0681
morphine
pH 7.5, 37°C, isozyme UGT1A8, at 2.5 mM morphine
0.2
morphine
isozyme UGT2B7 in COS-1 cell microsomes, pH 7.8, 37°C, in presence with CYP2C9
0.38
morphine
isozyme UGT2B7 in COS-1 cell microsomes, pH 7.8, 37°C
0.42
morphine
-
morphine 3-glucuronide formation, recombinant isozyme UGT2B7, pH 7.4, 37°C
0.48
morphine
isozyme UGT2B7 in COS-1 cell microsomes, pH 7.8, 37°C, in presence with CYP1A2
0.63
morphine
-
morphine 6-glucuronide formation, isozyme UGT2B7, pH 7.5, 37°C
0.67
morphine
-
morphine 3-glucuronide formation, isozyme UGT2B7, pH 7.5, 37°C
0.97
morphine
-
morphine 6-glucuronide formation, recombinant isozyme UGT2B7, pH 7.4, 37°C
1.18
morphine
liver microsomes, pH 7.8, 37°C
2.6
morphine
-
morphine 3-glucuronide formation, recombinant isozyme UGT1A8, pH 7.4, 37°C
3.2
morphine
-
morphine 3-glucuronide formation, recombinant isozyme UGT1A3, pH 7.4, 37°C
3.71
morphine
isozyme UGT2B7 in COS-1 cell microsomes, pH 7.8, 37°C, in presence with CYP3A4
7.3
morphine
-
membrane-bound recombinant isoform UGT1A10 from CHO cells, at pH 7.4 and 37°C
10.4
morphine
-
membrane-bound recombinant isoform UGT1A10 from HEK-293 cells, at pH 7.4 and 37°C
12.6
morphine
-
morphine 3-glucuronide formation, recombinant isozyme UGT1A10, pH 7.4, 37°C
18
morphine
-
morphine 3-glucuronide formation, recombinant isozyme UGT1A6, pH 7.4, 37°C
18.7
morphine
-
morphine 3-glucuronide formation, recombinant isozyme UGT1A1, pH 7.4, 37°C
37.4
morphine
-
morphine 3-glucuronide formation, recombinant isozyme UGT1A9, pH 7.4, 37°C
1.9
moxifloxacin

liver microsomes, pH 7.4, 37°C
2.1
moxifloxacin
isozyme UGT1A9, pH 7.4, 37°C
3.4
moxifloxacin
isozyme UGT1A1, pH 7.4, 37°C
0.046
Mycophenolic acid

-
mutant M33Q, pH 7.4, 37°C
0.087
Mycophenolic acid
-
wildtype, pH 7.4, 37°C
0.157
Mycophenolic acid
-
mutant M33I, pH 7.4, 37°C
0.16
Mycophenolic acid
-
isozyme UGT1A9
0.18
Mycophenolic acid
-
liver microsomes
0.2
Mycophenolic acid
-
mutant M33V, pH 7.4, 37°C
0.336
Mycophenolic acid
-
mutant M33T, pH 7.4, 37°C
0.072
naproxen

37°C, pH 7.4
0.25
naproxen
-
pH 7.4, 37°C
0.855
naproxen
37°C, pH 7.4
4.375
naproxen
37°C, pH 7.4
0.135
niflumic acid

-
0.0503
p-Cresol

pH not specified in the publication, temperature not specified in the publication
0.0584
p-Cresol
S50 value, n is 1.6, pH not specified in the publication, temperature not specified in the publication
5.06
p-ethoxyphenylurea

-
6.99
p-ethoxyphenylurea
-
0.0198
Phenylbutazone

C-glucuronidation
0.1951
Phenylbutazone
O-glucuronidation
0.0068
phloretin

isozyme UGT1A8, pH 7.0, 37°C
0.045
phloretin
isozyme UGT1A10, pH 6.4, 37°C
0.0964
phloretin
isozyme UGT1A7, pH 6.4, 37°C
0.0072
propofol

pH 7.4, 37°C, isozyme UGT1A9 in presence of 2% fatty acid-free human serum albumin
0.0106
propofol
pH 7.4, 37°C, liver microsomes in presence of 2% fatty acid-free human serum albumin
0.026
propofol
-
wildtype, pH 7.4, 37°C
0.041
propofol
pH 7.4, 37°C, isozyme UGT1A9
0.07
propofol
-
mutant M33Q, pH 7.4, 37°C
0.109
propofol
-
mutant M33V, pH 7.4, 37°C
0.113
propofol
-
mutant M33T, pH 7.4, 37°C
0.113
propofol
-
mutant M33I, pH 7.4, 37°C
0.127
propofol
pH 7.4, 37°C, liver microsomes
0.17
propofol
-
pH 7.5, 37°C, isozyme UGT1A9
0.5 - 1
propofol
UGT1A9/UGT2B7(mutant H35A)-CFP heterodimer, pH 7.4, 37°C
0.54
propofol
UGT1A9/UGT2B7(mutant DELTA C511-529)-CFP heterodimer, pH 7.4, 37°C
0.54
propofol
UGT1A9/UGT2B7(mutant DELTA C525-529)-CFP heterodimer, pH 7.4, 37°C
0.71
propofol
UGT1A9/UGT2B7(mutant DELTA N1-23)-CFP heterodimer, pH 7.4, 37°C
0.72
propofol
UGT1A9/UGT2B7-CFP heterodimer, pH 7.4, 37°C
0.72
propofol
UGT1A9/UGT2B7(mutant DELTA C493-529)-CFP heterodimer, pH 7.4, 37°C
0.76
propofol
UGT1A9 monomer, pH 7.4, 37°C
0.78
propofol
UGT1A9/UGT2B7(mutant N68A/N315A)-CFP heterodimer, pH 7.4, 37°C
0.86
propofol
UGT1A9/UGT2B7(mutant H268Y)-CFP heterodimer, pH 7.4, 37°C
0.9
propofol
UGT1A9/UGT2B7 heterodimer, pH 7.4, 37°C
0.211
Protocatechuic aldehyde

pH 7.5, 37°C, recombinant isozyme UGT1A6, formation of product M2
0.2385
Protocatechuic aldehyde
pH 7.5, 37°C, recombinant isozyme UGT1A9, formation of product M2
0.337
Protocatechuic aldehyde
pH 7.5, 37°C, liver microsomes, formation of product M2
0.3675
Protocatechuic aldehyde
pH 7.5, 37°C, recombinant isozyme UGT1A6, formation of product M1
0.38
Protocatechuic aldehyde
pH 7.5, 37°C, recombinant isozyme UGT1A9, formation of product M1
0.433
Protocatechuic aldehyde
pH 7.5, 37°C, liver microsomes, formation of product M1
0.494
Protocatechuic aldehyde
pH 7.5, 37°C, intestine microsomes, formation of product M2
0.627
Protocatechuic aldehyde
pH 7.5, 37°C, intestine microsomes, formation of product M1
0.032
retigabine

-
wildtype, pH 7.4, 37°C
0.055
retigabine
-
mutant M33Q, pH 7.4, 37°C
0.058
retigabine
-
mutant H37A
0.062
retigabine
-
mutant M33V, pH 7.4, 37°C
0.068
retigabine
-
mutant M33T, pH 7.4, 37°C
0.09
retigabine
-
wild-type
0.099
retigabine
-
mutant M33I, pH 7.4, 37°C
0.034
S-naproxen

-
pH 7.4, 37°C, renal cortex microsomes
0.045
S-naproxen
-
pH 7.4, 37°C, renal medulla microsomes
0.061
scopoletin

-
apparent Km for membrane-bound UGT1AB
0.062
scopoletin
-
mutant D143A
0.08
scopoletin
-
wild-type isozyme UGT1A9
0.083
scopoletin
-
wild-type
0.29
scopoletin
-
wild-type isozyme UGT1A6
0.629
scopoletin
-
mutant D148A
0.79
scopoletin
-
apparent Km for purified UGT1AB
0.954
scopoletin
-
mutant H37A
1.64
scopoletin
-
H369A mutant isozyme UGT1A9
3.88
scopoletin
-
H371A mutant isozyme UGT1A6
7.64
scopoletin
-
H379A mutant isozyme UGT1A6
3.7
serotonin

serotonin O-glucuronide formation, 1A4 co-expressed with isoform 1A6
4.4
serotonin
serotonin O-glucuronide formation, 1A4 co-expressed with isoform 1A4
4.6
serotonin
serotonin O-glucuronide formation
4.9
serotonin
lung UGT1A6, pH 7.5, 37°C
5.2 - 8.8
serotonin
liver UGT1A6, pH 7.5, 37°C
6.5
serotonin
kidney UGT1A6, pH 7.5, 37°C
8.6
serotonin
37°C, pH 7.4
9.8
serotonin
-
pH 7.5, 37°C, genetic variant UGT1A6*1
9.9
serotonin
-
pH 7.5, 37°C, genetic variant UGT1A6*1, co-expression of splice variants i1 and i2
12.4
serotonin
intestine UGT1A6, pH 7.5, 37°C
55.9
serotonin
recombinant UGT1A6 from lymphoblasts or insect cells, pH 7.5, 37°C
1.9
Sitafloxacin

isozyme UGT1A1, pH 7.4, 37°C
3.7
Sitafloxacin
liver microsomes, pH 7.4, 37°C
6.3
Sitafloxacin
isozyme UGT1A9, pH 7.4, 37°C
0.014
sulfinpyrazone

-
wildtype, pH 7.4, 37°C
0.032
sulfinpyrazone
-
mutant M33I, pH 7.4, 37°C
0.033
sulfinpyrazone
-
mutant M33Q, pH 7.4, 37°C
0.039
sulfinpyrazone
-
mutant M33V, pH 7.4, 37°C
0.053
sulfinpyrazone
-
mutant M33T, pH 7.4, 37°C
0.0038
testosterone

37°C, pH 7.4
0.0057
testosterone
37°C, pH 7.4
0.01
testosterone
-
isoform UGT2B17, pH 7.4, 37°C
0.0387
testosterone
-
isoform UGT2A1, pH 7.4, 37°C
0.007
tigogenin

recombinant mutant isozyme UGT1A4 L48V, pH 8.4, 37°C
0.008
tigogenin
recombinant wild-type isozyme UGT1A4, pH 8.4, 37°C
0.0056
tizoxanide

pH 7.4, 37°C
0.0155
tizoxanide
pH 7.4, 37°C
0.0506
tranilast

activity in human jejunum microsomes
0.0515
tranilast
activity in human liver microsomes
0.0037
trans-4-hydroxytamoxifen

-
isoform UGT2B7, variant 268His, pH 7.4, 37°C
0.004
trans-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT2B7
0.0087
trans-4-hydroxytamoxifen
-
isoform UGT2B7, variant 268Tyr, pH 7.4, 37°C
0.023
trans-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT1A8
0.023
trans-4-hydroxytamoxifen
-
isoform UGT1A8, variant 173Ala/277Cys, pH 7.4, 37°C
0.043
trans-4-hydroxytamoxifen
-
isoform UGT1A8, variant 173Gly/277Cys, pH 7.4, 37°C
0.052
trans-4-hydroxytamoxifen
-
isoform UGTA10, variant 139Lys, pH 7.4, 37°C
0.094
trans-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT1A3
0.096
trans-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT1A10
0.096
trans-4-hydroxytamoxifen
-
isoform UGTA10, variant 139Glu, pH 7.4, 37°C
0.124
trans-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT1A1
0.166
trans-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT1A7
0.319
trans-4-hydroxytamoxifen
pH 7.4, 37°C, isozyme UGT1A9
0.008
trans-androsterone

recombinant mutant isozyme UGT1A4 L48V, pH 8.4, 37°C
0.0236
trans-androsterone
-
isoform UGT1A4, pH 7.4, 37°C
0.255
trans-androsterone
recombinant wild-type isozyme UGT1A4, pH 8.4, 37°C
0.013
trans-endoxifen

-
isoform UGTA10, variant 139Lys, pH 7.4, 37°C
0.04
trans-endoxifen
-
isoform UGTA10, variant 139Glu, pH 7.4, 37°C
0.098
trans-endoxifen
-
isoform UGT1A8, variant 173Ala/277Cys, pH 7.4, 37°C
0.101
trans-endoxifen
-
isoform UGT2B7, variant 268His, pH 7.4, 37°C
0.101
trans-endoxifen
-
isoform UGT2B7, variant 268Tyr, pH 7.4, 37°C
0.135
trans-endoxifen
-
isoform UGT1A8, variant 173Gly/277Cys, pH 7.4, 37°C
0.0197
Trifluoperazine

trifluoperazine N-glucuronide formation
0.0198
Trifluoperazine
trifluoperazine N-glucuronide formation, 1A4 co-expressed with isoform 1A4
0.044
Trifluoperazine
-
isoform UGT1A4
0.048
Trifluoperazine
trifluoperazine N-glucuronide formation, 1A4 co-expressed with isoform 1A6
0.305
Trifluoperazine
-
isoform UGT1A1 mutant H39P
0.138
UDP-glucuronate

-
mutant D143A
0.173
UDP-glucuronate
-
mutant H37A
0.179
UDP-glucuronate
-
wild-type
0.184
UDP-glucuronate
-
mutant D148A
0.229
UDP-glucuronic acid

-
apparent Km for membrane-bound UGT1AB
0.704
UDP-glucuronic acid
-
apparent Km for purified UGT1AB
0.111
umbelliferone

isozyme UGT1A9, pH 7.4, 37°C
0.294
umbelliferone
isozyme UGT1A1, pH 7.4, 37°C
0.339
umbelliferone
isozyme UGT2B15, pH 7.4, 37°C
0.00579
xanthotoxol

enzyme from liver microsomes, at pH 7.4 and 37°C
0.0125
xanthotoxol
isoform UGT1A10, at pH 7.4 and 37°C
0.0345
xanthotoxol
enzyme from intestinal microsomes, at pH 7.4 and 37°C
0.04191
xanthotoxol
isoform UGT1A6, at pH 7.4 and 37°C
0.2024
xanthotoxol
isoform UGT1A8, at pH 7.4 and 37°C
0.2586
xanthotoxol
isoform UGT1A3, at pH 7.4 and 37°C
0.4593
xanthotoxol
isoform Ugt1a1, at pH 7.4 and 37°C
0.508
zidovudine

pH 7.4, 37°C, recombinant HA-tagged wild-type dimer
0.519
zidovudine
pH 7.4, 37°C, recombinant CFP-tagged mutant H268Y dimer
0.534
zidovudine
pH 7.4, 37°C, recombinant HA-tagged mutant A71S dimer
0.54
zidovudine
pH 7.4, 37°C, recombinant dimer of CFP-tagged H268Y and HA-tagged D398N mutant monomers
0.54
zidovudine
UGT1A9/UGT2B7(mutant DELTA C525-529)-CFP heterodimer, pH 7.4, 37°C
0.57
zidovudine
pH 7.4, 37°C, recombinant HA-tagged mutant H268Y dimer
0.589
zidovudine
pH 7.4, 37°C, recombinant dimer of CFP-tagged A71S and HA-tagged D398N mutant monomers
0.605
zidovudine
pH 7.4, 37°C, recombinant CFP-tagged wild-type dimer
0.605
zidovudine
pH 7.4, 37°C, recombinant dimer of CFP-tagged wild-type and HA-tagged D398N mutant monomers
0.609
zidovudine
pH 7.4, 37°C, recombinant dimer of CFP-tagged A71S and HA-tagged H268Y mutant monomers
0.634
zidovudine
pH 7.4, 37°C, recombinant CFP-tagged mutant A71S dimer
0.706
zidovudine
pH 7.4, 37°C, recombinant dimer of CFP-tagged wild-type and HA-tagged A71S mutant monomers
0.841
zidovudine
pH 7.4, 37°C, recombinant dimer of CFP-tagged wild-type and HA-tagged H268Y mutant monomers
0.94
zidovudine
UGT1A9/UGT2B7(mutant H268Y)-CFP heterodimer, pH 7.4, 37°C
0.97
zidovudine
UGT1A9/UGT2B7 heterodimer, pH 7.4, 37°C
1.05
zidovudine
UGT1A9/UGT2B7(mutant DELTA C511-529)-CFP heterodimer, pH 7.4, 37°C
1.06
zidovudine
UGT1A9/UGT2B7(mutant N68A/N315A)-CFP heterodimer, pH 7.4, 37°C
1.08
zidovudine
UGT1A9/UGT2B7-CFP heterodimer, pH 7.4, 37°C
1.54
zidovudine
UGT2B7-CFP monomer, pH 7.4, 37°C
additional information
additional information

Km values for 31 xenobiotics reported
-
additional information
additional information
-
Km values for all endogenous substrates for UGT2B7 range from 0.006 to 0.1 mM
-
additional information
additional information
kinetic analysis of UGT2B15, UGT2B17 and UGT2B20 mutant proteins for 5 alpha-androstane-3alpha-17beta-diol, dihydrotestosterone and testosterone
-
additional information
additional information
-
kinetic analysis of UGT2B15, UGT2B17 and UGT2B20 mutant proteins for 5 alpha-androstane-3alpha-17beta-diol, dihydrotestosterone and testosterone
-
additional information
additional information
kinetics
-
additional information
additional information
-
kinetics
-
additional information
additional information
kinetics
-
additional information
additional information
kinetics
-
additional information
additional information
kinetics
-
additional information
additional information
kinetics
-
additional information
additional information
-
kinetics
-
additional information
additional information
-
hyperbolic and sigmoidal kinetics for 4-methylumbelliferone and 1-naphthol for different isozymes, empirical and two-site models, overview
-
additional information
additional information
hyperbolic and sigmoidal kinetics for 4-methylumbelliferone and 1-naphthol for different isozymes, empirical and two-site models, overview
-
additional information
additional information
hyperbolic and sigmoidal kinetics for 4-methylumbelliferone and 1-naphthol for different isozymes, empirical and two-site models, overview
-
additional information
additional information
hyperbolic and sigmoidal kinetics for 4-methylumbelliferone and 1-naphthol for different isozymes, empirical and two-site models, overview
-
additional information
additional information
hyperbolic and sigmoidal kinetics for 4-methylumbelliferone and 1-naphthol for different isozymes, empirical and two-site models, overview
-
additional information
additional information
hyperbolic and sigmoidal kinetics for 4-methylumbelliferone and 1-naphthol for different isozymes, empirical and two-site models, overview
-
additional information
additional information
hyperbolic and sigmoidal kinetics for 4-methylumbelliferone and 1-naphthol for different isozymes, empirical and two-site models, overview
-
additional information
additional information
hyperbolic and sigmoidal kinetics for 4-methylumbelliferone and 1-naphthol for different isozymes, empirical and two-site models, overview
-
additional information
additional information
hyperbolic and sigmoidal kinetics for 4-methylumbelliferone and 1-naphthol for different isozymes, empirical and two-site models, overview
-
additional information
additional information
hyperbolic and sigmoidal kinetics for 4-methylumbelliferone and 1-naphthol for different isozymes, empirical and two-site models, overview
-
additional information
additional information
-
kinetics
-
additional information
additional information
-
different kinetic profiles of isozymes with different hormone substrates, overview
-
additional information
additional information
kinetics
-
additional information
additional information
-
kinetics
-
additional information
additional information
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kinetics
-
additional information
additional information
kinetics
-
additional information
additional information
kinetics
-
additional information
additional information
kinetics
-
additional information
additional information
kinetics
-
additional information
additional information
kinetics
-
additional information
additional information
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kinetics
-
additional information
additional information
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kinetics of microsomes from different tissues
-
additional information
additional information
kinetics, different isozymes, pH-values, and substrates
-
additional information
additional information
kinetics, different isozymes, pH-values, and substrates
-
additional information
additional information
kinetics, different isozymes, pH-values, and substrates
-
additional information
additional information
kinetics, different isozymes, pH-values, and substrates
-
additional information
additional information
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kinetics, different isozymes, pH-values, and substrates
-
additional information
additional information
-
kinetics
-
additional information
additional information
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kinetics, different isozymes
-
additional information
additional information
kinetics
-
additional information
additional information
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kinetics
-
additional information
additional information
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kinetics, at different conditions with different activators and different substrates, microsomes or recombinant isozymes, overview
-
additional information
additional information
-
imipramine N-glucuronide formation: Vmax (pmol/min/unit): 134.9, 110.4 (1A4 co-expressed with isoform 1A1), 126 (1A4 co-expressed with isoform 1A6). Trifluoperazine N-glucuronide formation: 2.1, 2.0 (1A4 co-expressed with isoform 1A1), 5.1 (1A4 co-expressed with isoform 1A6)
-
additional information
additional information
imipramine N-glucuronide formation: Vmax (pmol/min/unit): 134.9, 110.4 (1A4 co-expressed with isoform 1A1), 126 (1A4 co-expressed with isoform 1A6). Trifluoperazine N-glucuronide formation: 2.1, 2.0 (1A4 co-expressed with isoform 1A1), 5.1 (1A4 co-expressed with isoform 1A6)
-
additional information
additional information
-
coexpression of UGT1A1 decreases the Vmax value of UGT1A4-catalyzed imipramine N-glucuronide formation but has no effect on UGT1A4-catalyzed trifluoperazine N-glucuronide formation. Coexpression of UGT1A6 has no effect on UGT1A4-catalyzed imipramine N-glucuronide formation but increases the Km and Vmax of UGT1A4-catalyzed trifluoperazine N-glucuronide formation
-
additional information
additional information
coexpression of UGT1A1 decreases the Vmax value of UGT1A4-catalyzed imipramine N-glucuronide formation but has no effect on UGT1A4-catalyzed trifluoperazine N-glucuronide formation. Coexpression of UGT1A6 has no effect on UGT1A4-catalyzed imipramine N-glucuronide formation but increases the Km and Vmax of UGT1A4-catalyzed trifluoperazine N-glucuronide formation
-
additional information
additional information
-
serotonin O-glucuronide formation: Vmax (nmol/min/unit): 1.5, 2.1 (1A6 co-expressed with isoform 1A1), 6.1 (1A6 co-expressed with isoform 1A4). Diclofenac O-glucuronide formation: 0.0284, 0.088 (1A6 co-expressed with isoform 1A1), 0.0758 (1A6 co-expressed with isoform 1A4)
-
additional information
additional information
serotonin O-glucuronide formation: Vmax (nmol/min/unit): 1.5, 2.1 (1A6 co-expressed with isoform 1A1), 6.1 (1A6 co-expressed with isoform 1A4). Diclofenac O-glucuronide formation: 0.0284, 0.088 (1A6 co-expressed with isoform 1A1), 0.0758 (1A6 co-expressed with isoform 1A4)
-
additional information
additional information
-
co-expression of both UGT1A1 and UGT1A4 increases the Vmax values of UGT1A6-catalyzed serotonin and diclofenac O-glucuronide formation
-
additional information
additional information
co-expression of both UGT1A1 and UGT1A4 increases the Vmax values of UGT1A6-catalyzed serotonin and diclofenac O-glucuronide formation
-
additional information
additional information
-
kinetic analysis of wild-type isozyme UGT1A9 and mutants expressed in HEK293 cells, overview
-
additional information
additional information
kinetic analysis of wild-type isozyme UGT1A9 and mutants expressed in HEK293 cells, overview
-
additional information
additional information
kinetic analysis of wild-type isozyme UGT1A9 and mutants expressed in HEK293 cells, overview
-
additional information
additional information
kinetic analysis of wild-type isozyme UGT1A9 and mutants expressed in HEK293 cells, overview
-
additional information
additional information
kinetic analysis of wild-type isozyme UGT1A9 and mutants expressed in HEK293 cells, overview
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additional information
additional information
kinetic analysis, overview
-
additional information
additional information
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kinetic analysis, overview
-
additional information
additional information
kinetic modeling of the interactions between 4-methylumbelliferone, 1-naphthol, and zidovudine glucuronidation by UGT2B7 provides evidence for multiple substrate binding and effector sites, multisite kinetic equilibria models and two-site inhibition model for a substrate exhibiting Michaelis-Menten kinetics, three-site model for heteroactivation, overview
-
additional information
additional information
glucuronidation of the non-selective substrate 4-methylumbelliferone by mutant chimeric UGT2B7-15(61194)-7 and isozyme UGT2B15 followed MichaelisMenten and weak substrate inhibition kinetics, respectively, overview
-
additional information
additional information
glucuronidation of the non-selective substrate 4-methylumbelliferone by mutant chimeric UGT2B7-15(61194)-7 and isozyme UGT2B15 followed MichaelisMenten and weak substrate inhibition kinetics, respectively, overview
-
additional information
additional information
-
glucuronidation of the non-selective substrate 4-methylumbelliferone by mutant chimeric UGT2B7-15(61194)-7 and isozyme UGT2B15 followed MichaelisMenten and weak substrate inhibition kinetics, respectively, overview
-
additional information
additional information
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frusemide glucuronidation followed MichaelisMenten kinetics in all tissues, kinetics of different microsome types from liver and kidney, overview
-
additional information
additional information
-
-
additional information
additional information
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-
-
additional information
additional information
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kinetic analysis, isozyme UGT1A8 shows biphasic Michaelis-Menten kinetic behavior with substrate morphine, overview
-
additional information
additional information
kinetic analysis, isozyme UGT1A8 shows biphasic Michaelis-Menten kinetic behavior with substrate morphine, overview
-
additional information
additional information
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kinetic analysis, recombinant isozyme UGT1A4, and liver microsomes, with substrates dexmedetomidine and levomedetomidine, overview
-
additional information
additional information
kinetic analysis, recombinant isozyme UGT1A4, and liver microsomes, with substrates dexmedetomidine and levomedetomidine, overview
-
additional information
additional information
kinetics analysis using ecombinant isozymes UGT1A6 and UGT1A9, and liver and intestine microsomes, overview
-
additional information
additional information
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kinetics analysis using ecombinant isozymes UGT1A6 and UGT1A9, and liver and intestine microsomes, overview
-
additional information
additional information
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enzyme kinetics with substrate gemfibrozil follow Michaelis-Menten kinetics
-
additional information
additional information
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kinetics
-
additional information
additional information
kinetics
-
additional information
additional information
kinetics
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additional information
additional information
kinetics
-
additional information
additional information
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bisubstrate kinetics of wild-type and mutant isozyme UGT1A6
-
additional information
additional information
isozyme UGT1A4 with substrates nicotine and cotinine in liver and intestine microsomes
-
additional information
additional information
isozyme UGT1A4 with substrates nicotine and cotinine in liver and intestine microsomes
-
additional information
additional information
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isozyme UGT1A4 with substrates nicotine and cotinine in liver and intestine microsomes
-
additional information
additional information
glucuronidation of the non-selective substrate 4-methylumbelliferone by mutant chimeric UGT2B7-15(61194)-7 follows MichaelisMenten and weak substrate inhibition kinetics, respectively, whereas 4-methylumbelliferone glucuronidation by isozyme UGT2B7 exhibited sigmoidal kinetics characteristic of autoactivation, overview
-
additional information
additional information
glucuronidation of the non-selective substrate 4-methylumbelliferone by mutant chimeric UGT2B7-15(61194)-7 follows MichaelisMenten and weak substrate inhibition kinetics, respectively, whereas 4-methylumbelliferone glucuronidation by isozyme UGT2B7 exhibited sigmoidal kinetics characteristic of autoactivation, overview
-
additional information
additional information
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glucuronidation of the non-selective substrate 4-methylumbelliferone by mutant chimeric UGT2B7-15(61194)-7 follows MichaelisMenten and weak substrate inhibition kinetics, respectively, whereas 4-methylumbelliferone glucuronidation by isozyme UGT2B7 exhibited sigmoidal kinetics characteristic of autoactivation, overview
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additional information
additional information
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kinetic analysis, isozyme UGT1A1 shows biphasic Michaelis-Menten kinetic behavior with substrate morphine, overview
-
additional information
additional information
kinetic analysis, isozyme UGT1A1 shows biphasic Michaelis-Menten kinetic behavior with substrate morphine, overview
-
additional information
additional information
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kinetic analysis, recombinant isozyme UGT2B10, and liver microsomes, with substrates dexmedetomidine and levomedetomidine, overview
-
additional information
additional information
kinetic analysis, recombinant isozyme UGT2B10, and liver microsomes, with substrates dexmedetomidine and levomedetomidine, overview
-
additional information
additional information
kinetics of wild-type UGT1A6 and mutants, overview
-
additional information
additional information
kinetics of wild-type UGT1A6 and mutants, overview
-
additional information
additional information
kinetics of wild-type UGT1A6 and mutants, overview
-
additional information
additional information
kinetics of wild-type UGT1A6 and mutants, overview
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additional information
additional information
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kinetics of wild-type UGT1A6 and mutants, overview
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additional information
additional information
isozyme UGT2B10 with substrates nicotine and cotinine in liver and intestine microsomes
-
additional information
additional information
isozyme UGT2B10 with substrates nicotine and cotinine in liver and intestine microsomes
-
additional information
additional information
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isozyme UGT2B10 with substrates nicotine and cotinine in liver and intestine microsomes
-
additional information
additional information
Michaelis-Menten kinetics, overview
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additional information
additional information
Michaelis-Menten kinetics, overview
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additional information
additional information
Michaelis-Menten kinetics, overview
-
additional information
additional information
Michaelis-Menten kinetics, overview
-
additional information
additional information
Michaelis-Menten kinetics, overview
-
additional information
additional information
Michaelis-Menten kinetics, overview
-
additional information
additional information
Michaelis-Menten kinetics, overview
-
additional information
additional information
Michaelis-Menten kinetics, overview
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additional information
additional information
-
Michaelis-Menten kinetics, overview
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additional information
additional information
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steady-state kinetics, Michaelis-Menten kinetics
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additional information
additional information
Km values of isozymes using different specific substrates at different concentrations with healthy and hepatitis B virus-positive liver microsomes, overview
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additional information
additional information
Km values of isozymes using different specific substrates at different concentrations with healthy and hepatitis B virus-positive liver microsomes, overview
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additional information
additional information
Km values of isozymes using different specific substrates at different concentrations with healthy and hepatitis B virus-positive liver microsomes, overview
-
additional information
additional information
Km values of isozymes using different specific substrates at different concentrations with healthy and hepatitis B virus-positive liver microsomes, overview
-
additional information
additional information
-
Km values of isozymes using different specific substrates at different concentrations with healthy and hepatitis B virus-positive liver microsomes, overview
-
additional information
additional information
Michaelis-Menten kinetics
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additional information
additional information
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Michaelis-Menten kinetics
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additional information
additional information
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Michaelis-Menten kinetic modeling, overview
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additional information
additional information
Michaelis-Menten kinetic modeling, overview
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additional information
additional information
Q9Y4X1
Michaelis-Menten kinetic modeling, overview
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additional information
additional information
Michaelis-Menten and Hill kinetics
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additional information
additional information
Michaelis-Menten and Hill kinetics
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additional information
additional information
Michaelis-Menten and Hill kinetics
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additional information
additional information
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Michaelis-Menten and Hill kinetics
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additional information
additional information
substrate inhibition kinetics profile, overview
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additional information
additional information
substrate inhibition kinetics profile, overview
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additional information
additional information
substrate inhibition kinetics profile, overview
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additional information
additional information
substrate inhibition kinetics profile, overview
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additional information
additional information
substrate inhibition kinetics profile, overview
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additional information
additional information
substrate inhibition kinetics profile, overview
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additional information
additional information
substrate inhibition kinetics profile, overview
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additional information
additional information
substrate inhibition kinetics profile, overview
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additional information
additional information
substrate inhibition kinetics profile, overview
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additional information
additional information
substrate inhibition kinetics profile, overview
-
additional information
additional information
substrate inhibition kinetics profile, overview
-
additional information
additional information
substrate inhibition kinetics profile, overview
-
additional information
additional information
-
substrate inhibition kinetics profile, overview
-
additional information
additional information
Michaelis-Menten kinetic profile, overview
-
additional information
additional information
Michaelis-Menten kinetic profile, overview
-
additional information
additional information
Michaelis-Menten kinetic profile, overview
-
additional information
additional information
Michaelis-Menten kinetic profile, overview
-
additional information
additional information
Michaelis-Menten kinetic profile, overview
-
additional information
additional information
Michaelis-Menten kinetic profile, overview
-
additional information
additional information
Michaelis-Menten kinetic profile, overview
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additional information
additional information
Michaelis-Menten kinetic profile, overview
-
additional information
additional information
Michaelis-Menten kinetic profile, overview
-
additional information
additional information
Michaelis-Menten kinetic profile, overview
-
additional information
additional information
Michaelis-Menten kinetic profile, overview
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additional information
additional information
Michaelis-Menten kinetic profile, overview
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additional information
additional information
-
Michaelis-Menten kinetic profile, overview
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additional information
additional information
Michaelis-Menten kinetics with substrate 3-epideacetycinobufagin
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additional information
additional information
Michaelis-Menten kinetics
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additional information
additional information
Michaelis-Menten kinetics
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additional information
additional information
-
Michaelis-Menten kinetics
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additional information
additional information
Michaelis-Menten kinetics, kinetic parameters are determined for UGT3A2 using UDP-Glc or UDP-Xyl as cosubstrates
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additional information
additional information
Michaelis-Menten kinetics, kinetic parameters are determined for UGT3A2 using UDP-Glc or UDP-Xyl as cosubstrates
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additional information
additional information
-
Michaelis-Menten kinetics, kinetic parameters are determined for UGT3A2 using UDP-Glc or UDP-Xyl as cosubstrates
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additional information
additional information
Michaelis-Menten kinetics, kinetics analysis, overview. The kinetic analysis of PCP's and other chlorophenols' glucuronidation by human liver microsomes, the metabolic kinetic type is fit to the substrate inhibition model
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additional information
additional information
Michaelis-Menten kinetics, kinetics analysis, overview. The kinetic analysis of PCP's and other chlorophenols' glucuronidation by human liver microsomes, the metabolic kinetic type is fit to the substrate inhibition model
-
additional information
additional information
Michaelis-Menten kinetics, kinetics analysis, overview. The kinetic analysis of PCP's and other chlorophenols' glucuronidation by human liver microsomes, the metabolic kinetic type is fit to the substrate inhibition model
-
additional information
additional information
Michaelis-Menten kinetics, kinetics analysis, overview. The kinetic analysis of PCP's and other chlorophenols' glucuronidation by human liver microsomes, the metabolic kinetic type is fit to the substrate inhibition model
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