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TargetCarboxypeptidase B2
LigandBDBM109260
Substrate/Competitorn/a
Meas. Tech.Enzyme Inhibition Assay
IC50 10±n/a nM
Citation Nagata, TInoue, MAshida, YNoguchi, KOno, M Cycloalkyl-substituted imidazole derivative US Patent US8609710 Publication Date 12/17/2013
More Info.:Get all data from this article,  Assay Method
 
Carboxypeptidase B2
Name:Carboxypeptidase B2
Synonyms:CBPB2_HUMAN | CPB2 | CPU | Carboxypeptidase B2 | Carboxypeptidase B2 isoform A | Carboxypeptidase U | Plasma carboxypeptidase B | TAFI | Thrombin-activable fibrinolysis inhibitor | pCPB
Type:Enzyme
Mol. Mass.:48432.74
Organism:Homo sapiens (Human)
Description:Q96IY4
Residue:423
Sequence:
MKLCSLAVLVPIVLFCEQHVFAFQSGQVLAALPRTSRQVQVLQNLTTTYEIVLWQPVTAD
LIVKKKQVHFFVNASDVDNVKAHLNVSGIPCSVLLADVEDLIQQQISNDTVSPRASASYY
EQYHSLNEIYSWIEFITERHPDMLTKIHIGSSFEKYPLYVLKVSGKEQAAKNAIWIDCGI
HAREWISPAFCLWFIGHITQFYGIIGQYTNLLRLVDFYVMPVVNVDGYDYSWKKNRMWRK
NRSFYANNHCIGTDLNRNFASKHWCEEGASSSSCSETYCGLYPESEPEVKAVASFLRRNI
NQIKAYISMHSYSQHIVFPYSYTRSKSKDHEELSLVASEAVRAIEKISKNTRYTHGHGSE
TLYLAPGGGDDWIYDLGIKYSFTIELRDTGTYGFLLPERYIKPTCREAFAAVSKIAWHVI
RNV
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BDBM109260
n/a
NameBDBM109260
Synonyms:US8609710, 36
TypeSmall organic molecule
Emp. Form.C18H31N3O2
Mol. Mass.321.4576
SMILESCCC(CN)CC(Cc1cn(cn1)[C@H]1CC[C@H](C)CC1)C(O)=O |r,wU:13.13,wD:16.17,(4.8,-.52,;3.47,-1.29,;2.14,-.52,;2.14,1.02,;3.47,1.79,;.8,-1.29,;.8,-2.83,;-.53,-3.6,;-1.86,-2.83,;-1.86,-1.29,;-3.33,-.81,;-4.23,-2.06,;-3.33,-3.3,;-3.73,.68,;-5.22,1.07,;-5.61,2.56,;-4.53,3.65,;-4.92,5.14,;-3.04,3.25,;-2.64,1.76,;2.14,-3.6,;2.14,-5.14,;3.47,-2.83,)|
Structure
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