Reaction Details  Report a problem with these data
Target
Carboxypeptidase B2
Ligand
BDBM109239
Substrate
n/a
Meas. Tech.
Enzyme Inhibition Assay
IC50
8.8±n/a nM
Citation
 Nagata, T; Inoue, M; Ashida, Y; Noguchi, K; Ono, M Cycloalkyl-substituted imidazole derivative US Patent  US8609710 Publication Date 12/17/2013
Target
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:
MKLCSLAVLVPIVLFCEQHVFAFQSGQVLAALPRTSRQVQVLQNLTTTYEIVLWQPVTADLIVKKKQVHFFVNASDVDNVKAHLNVSGIPCSVLLADVEDLIQQQISNDTVSPRASASYYEQYHSLNEIYSWIEFITERHPDMLTKIHIGSSFEKYPLYVLKVSGKEQAAKNAIWIDCGIHAREWISPAFCLWFIGHITQFYGIIGQYTNLLRLVDFYVMPVVNVDGYDYSWKKNRMWRKNRSFYANNHCIGTDLNRNFASKHWCEEGASSSSCSETYCGLYPESEPEVKAVASFLRRNINQIKAYISMHSYSQHIVFPYSYTRSKSKDHEELSLVASEAVRAIEKISKNTRYTHGHGSETLYLAPGGGDDWIYDLGIKYSFTIELRDTGTYGFLLPERYIKPTCREAFAAVSKIAWHVIRNV
  
Inhibitor
Name:
BDBM109239
Synonyms:
US8609710, 3
Type:
Small organic molecule
Emp. Form.:
C17H29N3O2
Mol. Mass.:
307.4311
SMILES:
CC[C@H]1CC[C@@H](CC1)n1cnc(CC(CCCN)C(O)=O)c1 |r,wU:5.8,wD:2.1,(-4.94,5.34,;-3.45,4.94,;-3.05,3.45,;-4.14,2.36,;-3.74,.87,;-2.26,.48,;-1.17,1.57,;-1.57,3.05,;-1.86,-1.01,;-2.76,-2.26,;-1.86,-3.5,;-.39,-3.03,;.94,-3.8,;2.27,-3.03,;2.27,-1.49,;3.61,-.72,;3.61,.82,;4.94,1.59,;3.61,-3.8,;3.61,-5.34,;4.94,-3.03,;-.39,-1.49,)|
Structure:
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