Reaction Details | |||
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Target | Carboxypeptidase B2 | ||
Ligand | BDBM109260 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Enzyme Inhibition Assay | ||
IC50 | 10±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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BDBM109260 | |||
n/a | |||
Name | BDBM109260 | ||
Synonyms: | US8609710, 36 | ||
Type | Small organic molecule | ||
Emp. Form. | C18H31N3O2 | ||
Mol. Mass. | 321.4576 | ||
SMILES | CCC(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 |