Reaction Details | |||
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Target | Carboxypeptidase B2 | ||
Ligand | BDBM109254 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Enzyme Inhibition Assay | ||
IC50 | 7.0±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 | ||
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: |
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BDBM109254 | |||
n/a | |||
Name | BDBM109254 | ||
Synonyms: | US8609710, 25 | ||
Type | Small organic molecule | ||
Emp. Form. | C16H27N3O3 | ||
Mol. Mass. | 309.4039 | ||
SMILES | C[C@H](CN)OC(Cc1cn(cn1)[C@H]1CC[C@H](C)CC1)C(O)=O |r,wU:12.12,1.0,wD:15.16,(4.54,-1.29,;3.21,-.52,;3.21,1.02,;4.54,1.79,;1.87,-1.29,;1.87,-2.83,;.54,-3.6,;-.79,-2.83,;-.79,-1.29,;-2.26,-.81,;-3.16,-2.06,;-2.26,-3.3,;-2.66,.68,;-4.14,1.07,;-4.54,2.56,;-3.45,3.65,;-3.85,5.14,;-1.97,3.25,;-1.57,1.76,;3.21,-3.6,;3.21,-5.14,;4.54,-2.83,)| | ||
Structure |