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Information on EC 1.14.13.67 - quinine 3-monooxygenase Word Map on EC 1.14.13.67
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The enzyme appears in viruses and cellular organisms
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quinine + NADPH + H+ + O2 = 3-hydroxyquinine + NADP+ + H2O
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quinine,NADPH:oxygen oxidoreductase
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cytochrome P450 isoform
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Nifedipine oxidase
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quinine 3-hydroxylase
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Quinine 3-monooxygenase
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CYP3A4
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mouse
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rat
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UniProt
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human
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physiological function
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differences in the activity of both CYP3A4 and CYP3A5 in Koreans, Swedes and Tanzanians. Both 4beta-hydroxycholesterol and quinine/3-hydroxyquinine metabolic ratio show a higher CYP3A activity in women than in men
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etoposide + NADPH + O2
3'-demethyletoposide + NADP+ + H2O
quinine + NADPH + H+ + O2
3-hydroxyquinine + NADP+ + H2O
quinine + NADPH + O2
3-hydroxyquinine + NADP+ + H2O
teniposide + NADPH + O2
teniposide catechol + NADP+ + H2O
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etoposide + NADPH + O2
3'-demethyletoposide + NADP+ + H2O
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etoposide + NADPH + O2
3'-demethyletoposide + NADP+ + H2O
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quinine + NADPH + H+ + O2
3-hydroxyquinine + NADP+ + H2O
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quinine + NADPH + H+ + O2
3-hydroxyquinine + NADP+ + H2O
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quinine + NADPH + H+ + O2
3-hydroxyquinine + NADP+ + H2O
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quinine + NADPH + O2
3-hydroxyquinine + NADP+ + H2O
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quinine + NADPH + O2
3-hydroxyquinine + NADP+ + H2O
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quinine + NADPH + O2
3-hydroxyquinine + NADP+ + H2O
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quinine + NADPH + O2
3-hydroxyquinine + NADP+ + H2O
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quinine + NADPH + O2
3-hydroxyquinine + NADP+ + H2O
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quinine is used for treatment of severe forms of Plasmodium falciparum malaria, phenotyping of two different populations, overview
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quinine + NADPH + O2
3-hydroxyquinine + NADP+ + H2O
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quinine + NADPH + O2
3-hydroxyquinine + NADP+ + H2O
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quinine + NADPH + H+ + O2
3-hydroxyquinine + NADP+ + H2O
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quinine + NADPH + O2
3-hydroxyquinine + NADP+ + H2O
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quinine is used for treatment of severe forms of Plasmodium falciparum malaria, phenotyping of two different populations, overview
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anti-CYP2C antibodies
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inhibition of 20%
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etoposide
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maximum inhibition of quinine 3-hydroxylation of 60% at 0.1 mM
grape seed extract
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inhibition ranges from 6.4% to 26.8% dependent on the product
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green tea extract
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most pronounced inhibition of CYP3A4, which ranges from 5.6% to 89.9% dependent on the product
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ketoconazole 2R,4R enantiomer
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ketoconazole 2R,4S enantiomer
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ketoconazole 2S,4R enantiomer
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ketoconazole 2S,4S enantiomer
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Quinine
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maximum inhibition of etoposide 3'-demethylation of 52% at 0.1 mM
sulfaphenazole
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inhibits more than 50% at 0.1 mM
additional information
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ginseng products have little to no effect on the activity of CYP3A4
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alpha-naphthoflavone
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anti-CYP3A4 antibodies
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inhibition of 92%
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anti-CYP3A4 antibodies
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inhibition of 72%
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anti-CYP3A4 antibodies
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anti-CYP3A4 antibodies
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inhibition of 96%
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anti-CYP3A4 antibodies
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inhibition of 84%
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Chloroquin
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diazepam
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doxycyclin
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ketoconazole
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maximum inhibition of 88%
ketoconazole
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maximum inhibition of 90% at 0.0005 mM
ketoconazole
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maximum inhibition of 90% at 0.001 mM
ketoconazole
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maximum inhibition of 90%
ketoconazole
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i.e. KTZ, is a antifungal drug, known as an inhibitor of, especially, the CYP3A subfamily, KTZ racemate and four separate enantiomers are evaluated for their selectivity in inhibiting quinine metabolism
ketoconazole
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maximum inhibition of 94%
ketoconazole
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maximum inhibition of 91%
p-nitrophenol
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inhibition observed but not quantified
p-nitrophenol
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inhibits more than 75% at 10 mM
primaquine
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S-mephenytoin
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maximum inhibition of 74% at 0.12 mM
S-mephenytoin
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inhibits more than 70% at 0.5 mM
tetracyclin
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troleandomycin
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maximum inhibition of 93%
troleandomycin
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maximum inhibition of 70% at 0.08 mM
troleandomycin
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maximum inhibition of 80% at 0.1 mM
troleandomycin
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maximum inhibition of 70%
troleandomycin
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maximum inhibition of 85%
troleandomycin
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maximum inhibition of 66%
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grape seed extract
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some brands cause minor activation of CYP3A4
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alpha-naphthoflavone
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diazepam
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additional information
etoposide
0.0227
Quinine
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0.046
Quinine
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recombinant CYP2C19
0.106
Quinine
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between 0.08 mM and 0.145 mM in 10 different human livers
0.114
Quinine
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recombinant CYP3A4
additional information
etoposide
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between 0.0421 mM and 0.1151 mM
additional information
additional information
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kinetics
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additional information
tenoposide
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between 0.0197 mM and 0.0435 mM
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0.00327
Quinine
Homo sapiens
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recombinant CYP2C19
0.125
Quinine
Homo sapiens
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recombinant CYP3A4
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0.023
ketoconazole 2R,4R enantiomer
Homo sapiens
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pH 7.4, 37°C
0.014
ketoconazole 2R,4S enantiomer
Homo sapiens
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pH 7.4, 37°C
0.011
ketoconazole 2S,4R enantiomer
Homo sapiens
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pH 7.4, 37°C
0.004
ketoconazole 2S,4S enantiomer
Homo sapiens
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pH 7.4, 37°C
0.01
ketoconazole racemate
Homo sapiens
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pH 7.4, 37°C
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native enzyme partially by microsome preparation
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expression of CYP3A4 in human B lymphoblastoid cell line AHH-1
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genes CYP3A5 and CYP3A4, DNA sequence determination, genotyping of two different human populations revealing the CYP3A5 and the CYP3A4 genotypes
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A6986AG
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single nucleotide polymorphism responsible for different CYP3A genotypes, CYP3A5 allele and genotype frequency in the populations, overview
additional information
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the CYP3A5 genotype has significant effect on quinine 3-hydroxylation in black Tanzanians, who have lower total CYP3A activity compared to a population of Swedish caucasians, overview
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medicine
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green tea extract use may cause significant interactions with drugs metabolized by CYP3A4. Effect on CYP3A4 varies among different brands of green tea extract, possibly due to variations in their content of the herbal product's active ingredients
medicine
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plasma concentration of 4beta-hydroxycholesterol may be used as an endogenous marker of CYP3A activity
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CP3A4_HUMAN
503
57343
Swiss-Prot
B7P1N3_IXOSC
259
29542
TrEMBL
B7PVW8_IXOSC
419
47479
TrEMBL
B7PVW8_IXOSC
419
47479
TrEMBL
B7PWV9_IXOSC
146
16730
TrEMBL
B7PKJ0_IXOSC
159
18245
TrEMBL
B7Q2U5_IXOSC
498
57077
TrEMBL
B7P2B2_IXOSC
204
23463
TrEMBL
B7PME9_IXOSC
524
60217
TrEMBL
B7P5J6_IXOSC
278
31788
TrEMBL
B7P714_IXOSC
163
18794
TrEMBL
B7P0T1_IXOSC
178
20949
TrEMBL
B7QDA0_IXOSC
504
57487
TrEMBL
E0VSD4_PEDHC
Pediculus humanus subsp. corporis
529
61663
TrEMBL
B7Q3W6_IXOSC
135
15185
TrEMBL
B7PFG4_IXOSC
180
20790
TrEMBL
B7P474_IXOSC
185
21199
TrEMBL
B7PSW1_IXOSC
280
31440
TrEMBL
B7P0T0_IXOSC
202
23253
TrEMBL
B7P1N5_IXOSC
189
21341
TrEMBL
B7PVW7_IXOSC
508
58183
TrEMBL
B7PES7_IXOSC
363
41726
TrEMBL
B7P2B0_IXOSC
208
24239
TrEMBL
B7QJP4_IXOSC
135
15355
TrEMBL
B7Q1D1_IXOSC
140
16124
TrEMBL
B7QD99_IXOSC
209
24137
TrEMBL
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Zhao, X.J.; Yokoyama, H.; Chiba, K.; Wanwimolruk, S.; Ishizaki, T.
Identification of human cytochrome P450 isoforms involved in the hydroxylation of quinine by human liver microsomes and nine recombinant human cytochromes P450
J. Pharmacol. Exp. Ther.
279
1327-1334
1996
Homo sapiens
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Zhao, X.J.; Kawashiro, T.; Ishizaki, T.
Mutual inhibition between quinine and etoposide by human liver microsomes. Evidence for cytochrome P4503A4 involvement in their major metabolic pathways
Drug Metab. Dispos.
26
188-191
1997
Homo sapiens
brenda
Zhao, X.J.; Ishizaki, T.
The in vitro hepatic metabolism of quinine in mice, rats and dogs: comparison with human liver microsomes
J. Pharmacol. Exp. Ther.
283
1168-1176
1997
Canis lupus familiaris, Homo sapiens, Mus musculus, Rattus norvegicus
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Relling, M.V.; Evans, R.; Dass, C.; Desiderio, D.M.; Nemec, J.
Human cytochrome P450 metabolism of teniposide and etoposide
J. Pharmacol. Exp. Ther.
261
491-496
1992
Homo sapiens
brenda
Mirghani, R.A.; Sayi, J.; Aklillu, E.; Allqvist, A.; Jande, M.; Wennerholm, A.; Eriksen, J.; Herben, V.M.; Jones, B.C.; Gustafsson, L.L.; Bertilsson, L.
CYP3A5 genotype has significant effect on quinine 3-hydroxylation in Tanzanians, who have lower total CYP3A activity than a Swedish population
Pharmacogenet. Genomics
16
637-645
2006
Homo sapiens
brenda
Allqvist, A.; Miura, J.; Bertilsson, L.; Mirghani, R.A.
Inhibition of CYP3A4 and CYP3A5 catalyzed metabolism of alprazolam and quinine by ketoconazole as racemate and four different enantiomers
Eur. J. Clin. Pharmacol.
63
173-179
2007
Homo sapiens
brenda
Wanwimolruk, S.; Wong, K.; Wanwimolruk, P.
Variable inhibitory effect of different brands of commercial herbal supplements on human cytochrome P-450 CYP3A4
Drug Metabol. Drug Interact.
24
17-35
2009
Homo sapiens, Homo sapiens (P08684)
brenda
Diczfalusy, U.; Miura, J.; Roh, H.K.; Mirghani, R.A.; Sayi, J.; Larsson, H.; Bodin, K.G.; Allqvist, A.; Jande, M.; Kim, J.W.; Aklillu, E.; Gustafsson, L.L.; Bertilsson, L.
4Beta-hydroxycholesterol is a new endogenous CYP3A marker: relationship to CYP3A5 genotype, quinine 3-hydroxylation and sex in Koreans, Swedes and Tanzanians
Pharmacogenet. Genomics
18
201-208
2008
Homo sapiens, Homo sapiens (P08684)
brenda
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