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3.4.17.20: Carboxypeptidase U

This is an abbreviated version!
For detailed information about Carboxypeptidase U, go to the full flat file.

Word Map on EC 3.4.17.20

Reaction

release of C-terminal Arg and Lys from a polypeptide =

Synonyms

aCAP, activated thrombin activable fibrinolysis inhibitor, activated thrombin-activable fibrinolysis inhibitor, activated thrombin-activatable fibrinolysis inhibitor, active carboxypeptidase B, active thrombin-activatable fibrinolysis inhibitor, Arginine carboxypeptidase, Carboxypeptidase B, pro-, carboxypeptidase B2, Carboxypeptidase R, carboxypeptidase U, Carboxypeptidase-U, CPB2, CPR, CPU, Plasma carboxypeptidase B, plasma carboxypeptidase U, plasma CPB, plasma procarboxypeptidase B, plasma procarboxypeptidase B-like proenzyme, plasma procarboxypeptidase U, pro-pCPB, Procarboxypeptidase B, procarboxypeptidase R, procarboxypeptidase U, proCPU, pTAFI, rTAFI, TAFI, TAFIa, TFAI, thrombin activable fibrinolysis inhibitor, thrombin activatable fibrinolysis inhibitor, Thrombin-activable fibrinolysis inhibitor, thrombin-activatable fibrinolysis inhibitor

ECTree

     3 Hydrolases
         3.4 Acting on peptide bonds (peptidases)
             3.4.17 Metallocarboxypeptidases
                3.4.17.20 Carboxypeptidase U

IC50 Value

IC50 Value on EC 3.4.17.20 - Carboxypeptidase U

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IC50 VALUE [mM]
INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
0.000003
(R)-2-(3-guanidinophenyl)-3-mercaptopropanoic acid
Homo sapiens
-
-
0.0000007
(R)-3-(2-aminoethylthio)-2-(3-((R)-3-cyclohexyl-1-oxo-1-((1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ylamino)propan-2-yl)ureido)propanoic acid
Homo sapiens
-
-
0.044
(S)-2,5-dihydroxy-N-(1-hydroxy-3-phenylpropan-2-yl)benzamide
Homo sapiens
-
-
0.0032
2-(2-amino-pyridin-4-ylmethyl)-3-mercapto-propionic acid
Homo sapiens
-
reversible inhibition, IC50: 0.0032 mM
0.0044
2-(2-guanidinoethylthio)succinic acid
Homo sapiens
-
-
0.000003
2-(3-carbamimidamidophenyl)-3-sulfanylpropanoic acid
Homo sapiens
-
-
0.25
2-(6-amino-pyridin-3-ylmethyl)-2-mercaptomethyl-butyric acid
Homo sapiens
-
reversible inhibition, IC50: 0.25 mM
0.0005
2-mercaptomethyl-3-(6-amino-pyridin-3-yl)-2-fluoro-propionic acid
Homo sapiens
-
reversible inhibition, IC50: 0.0005 mM
0.0009
2-mercaptomethyl-3-(6-amino-pyridin-3-yl)-2-hydroxy-propionic acid
Homo sapiens
-
reversible inhibition, IC50: 0.0009 mM
0.0032
2-mercaptomethyl-3-piperidin-4-yl-propionic acid
Homo sapiens
-
reversible inhibition, IC50: 0.0032 mM
0.0016
2-mercaptomethyl-3-pyrrolidin-3-yl-propionic acid
Homo sapiens
-
reversible inhibition, IC50: 0.0016 mM
0.0013
3-(2-amino-thiazol-5-yl)-2-mercaptomethyl-propionic acid
Homo sapiens
-
reversible inhibition, IC50: 0.0013 mM
0.0002
3-(2-guanidinoethylthio)-2-(mercaptomethyl)propanoic acid
Homo sapiens
-
-
0.0063
3-(6-amino-2-methyl-pyridin-3-yl)-2-mercaptomethyl-propionic acid
Homo sapiens
-
reversible inhibition, IC50: 0.0063 mM
0.0079
3-(6-amino-4-methyl-pyridin-3-yl)-2-mercaptomethyl-propionic acid
Homo sapiens
-
reversible inhibition, IC50: 0.0079 mM
0.01
3-(6-amino-5-chloro-pyridin-3-yl)-2-mercaptomethyl-propionic acid
Homo sapiens
-
reversible inhibition, IC50: 0.010 mM
0.013
3-(6-amino-5-hydroxymethyl-pyridin-3-yl)-2-mercaptomethyl-propionic acid
Homo sapiens
-
reversible inhibition, IC50: 0.013 mM
0.083
3-(6-amino-5-methyl-pyridin-3-yl)-2-(hydroxymethyl)-2-mercaptomethyl-propionic acid
Homo sapiens
-
reversible inhibition, IC50: 0.083 mM
0.001 - 0.0016
3-(6-amino-5-methyl-pyridin-3-yl)-2-mercaptomethyl-2-methyl-propionic acid
0.0006
3-(6-amino-pyridin-3-yl)-2-mercaptomethyl-2-methyl-propionic acid
Homo sapiens
-
reversible inhibition, IC50: 0.0006 mM
0.0002
3-(6-amino-pyridin-3-yl)-2-mercaptomethyl-propionic acid
Homo sapiens
-
reversible inhibition, IC50: 0.0002 mM
0.000004
3-(6-aminopyridin-3-yl)-2-(1-((5-(5-chlorothiophen-2-yl)isoxazol-3-yl)methyl)-1H-imidazol-4-yl)propanoic acid
Homo sapiens
-
-
0.000002
3-(6-aminopyridin-3-yl)-2-(1-isopentyl-1H-imidazol-4-yl)propanoic acid
Homo sapiens
-
-
0.000001
3-(6-aminopyridin-3-yl)-2-(1H-imidazol-4-yl)propanoic acid
Homo sapiens
-
IC50: 0.000001 mM
0.0002
3-(6-aminopyridin-3-yl)-2-(mercaptomethyl)propanoic acid
Homo sapiens
-
-
0.000002
3-(6-aminopyridin-3-yl)-2-[1-(3-methylbutyl)-1H-imidazol-4-yl]propanoic acid
Homo sapiens
-
-
0.001
3-(cis-4-amino-cyclopent-2-yl)-2-mercaptomethyl-propionic acid
Homo sapiens
-
reversible inhibition, IC50: 0.001 mM
0.02
3-[(2-carbamimidamidoethyl)sulfanyl]-2-(sulfanylmethyl)propanoic acid
Homo sapiens
-
reversible inhibition, IC50: 0.02 mM
0.27
5-bromo-4-chloro-indolyl beta-D-galactopyranosyl-alpha-2,6-N-acetyl-neuraminic acid
Homo sapiens
-
reversible inhibition, IC50: 0.27 mM
0.0002
anabaenopeptin-type cyclic peptide
Homo sapiens
-
-
-
0.000002
BX-528
Homo sapiens
-
-
0.029
DL-mercaptomethyl-3-guanidinoethylthiopropanoic acid
Homo sapiens
-
i.e. Plummer's inhibitor, IC50: 0.029 mM
0.0000083
EF-6265
Homo sapiens
-
-
0.000001 - 0.00000826
EF6265
0.0094
guanidinyl-L-cysteine
Homo sapiens
-
IC50: 0.0094 mM in inhibition of plasma fibrin clot lysis
0.0000083
[(S)-7-amino-2-[[[(R)-2-methyl-1-(3-phenylpropanoylamino)propyl]hydroxyphosphinoyl]methyl]heptanoic acid]
Homo sapiens
-
IC50: 8.3 nM, potent and highly selective inhibitor. Systemically administered inhibitor enhances fibrinolysis in a dose- and time-dependent manner