| Reaction Details |
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 | Report a problem with these data |
| Target | Carboxypeptidase A1 |
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| Ligand | BDBM50135933 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_45620 (CHEMBL655431) |
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| IC50 | >50000±n/a nM |
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| Citation |  Barrow, JC; Nantermet, PG; Stauffer, SR; Ngo, PL; Steinbeiser, MA; Mao, SS; Carroll, SS; Bailey, C; Colussi, D; Bosserman, M; Burlein, C; Cook, JJ; Sitko, G; Tiller, PR; Miller-Stein, CM; Rose, M; McMasters, DR; Vacca, JP; Selnick, HG Synthesis and evaluation of imidazole acetic acid inhibitors of activated thrombin-activatable fibrinolysis inhibitor as novel antithrombotics. J Med Chem46:5294-7 (2003) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| Carboxypeptidase A1 |
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| Name: | Carboxypeptidase A1 |
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| Synonyms: | CBPA1_HUMAN | CPA | CPA1 |
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| Type: | PROTEIN |
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| Mol. Mass.: | 47132.61 |
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| Organism: | Homo sapiens (Human) |
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| Description: | ChEMBL_1496378 |
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| Residue: | 419 |
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| Sequence: | MRGLLVLSVLLGAVFGKEDFVGHQVLRISVADEAQVQKVKELEDLEHLQLDFWRGPAHPG
SPIDVRVPFPSIQAVKIFLESHGISYETMIEDVQSLLDEEQEQMFAFRSRARSTDTFNYA
TYHTLEEIYDFLDLLVAENPHLVSKIQIGNTYEGRPIYVLKFSTGGSKRPAIWIDTGIHS
REWVTQASGVWFAKKITQDYGQDAAFTAILDTLDIFLEIVTNPDGFAFTHSTNRMWRKTR
SHTAGSLCIGVDPNRNWDAGFGLSGASSNPCSETYHGKFANSEVEVKSIVDFVKDHGNIK
AFISIHSYSQLLMYPYGYKTEPVPDQDELDQLSKAAVTALASLYGTKFNYGSIIKAIYQA
SGSTIDWTYSQGIKYSFTFELRDTGRYGFLLPASQIIPTAKETWLALLTIMEHTLNHPY
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| BDBM50135933 |
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| n/a |
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| Name | BDBM50135933 |
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| Synonyms: | 3-(6-Amino-pyridin-3-yl)-2-(1H-imidazol-4-yl)-propionic acid | CHEMBL302067 |
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| Type | Small organic molecule |
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| Emp. Form. | C11H12N4O2 |
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| Mol. Mass. | 232.2386 |
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| SMILES | Nc1ccc(CC(C(O)=O)c2cnc[nH]2)cn1 |
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| Structure | 
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