Reaction Details | |||
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Target | Carboxypeptidase B2 | ||
Ligand | BDBM109239 | ||
Substrate/Competitor | 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 | ||
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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BDBM109239 | |||
n/a | |||
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 |