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TargetCarboxypeptidase B2
LigandBDBM109240
Substrate/Competitorn/a
Meas. Tech.Enzyme Inhibition Assay
IC50 14±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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BDBM109240
n/a
NameBDBM109240
Synonyms:US8609710, 4
TypeSmall organic molecule
Emp. Form.C15H25N3O2
Mol. Mass.279.3779
SMILESCCC1CC(C1)n1cnc(CC(CCCN)C(O)=O)c1 |(-4.82,4.9,;-3.34,4.5,;-2.94,3.02,;-1.6,2.25,;-2.37,.91,;-3.71,1.68,;-1.98,-.58,;-2.88,-1.82,;-1.98,-3.07,;-.51,-2.59,;.82,-3.36,;2.16,-2.59,;2.16,-1.05,;3.49,-.28,;3.49,1.26,;4.82,2.03,;3.49,-3.36,;3.49,-4.9,;4.82,-2.59,;-.51,-1.05,)|
Structure
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