Reaction Details |
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Target | Carboxypeptidase N catalytic chain |
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Ligand | BDBM50275212 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1714519 (CHEMBL4124568) |
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IC50 | >380000±n/a nM |
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Citation | Itoh, T; Yoshimoto, N; Hirano, Y; Yamamoto, K Structural basis for the selective inhibition of activated thrombin-activatable fibrinolysis inhibitor (TAFIa) by a selenium-containing inhibitor with chloro-aminopyridine as a basic group. Bioorg Med Chem Lett28:2256-2260 (2018) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carboxypeptidase N catalytic chain |
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Name: | Carboxypeptidase N catalytic chain |
Synonyms: | ACBP | Anaphylatoxin inactivator | Arginine carboxypeptidase | CBPN_HUMAN | CPN | CPN1 | Carboxypeptidase N catalytic chain | Carboxypeptidase N polypeptide 1 | Carboxypeptidase N small subunit | Carboxypeptidase N, catalytic subunit | Kininase-1 | Lysine carboxypeptidase | Plasma carboxypeptidase B | SCPN | Serum carboxypeptidase N |
Type: | PROTEIN |
Mol. Mass.: | 52293.66 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1496379 |
Residue: | 458 |
Sequence: | MSDLLSVFLHLLLLFKLVAPVTFRHHRYDDLVRTLYKVQNECPGITRVYSIGRSVEGRHL
YVLEFSDHPGIHEPLEPEVKYVGNMHGNEALGRELMLQLSEFLCEEFRNRNQRIVQLIQD
TRIHILPSMNPDGYEVAAAQGPNKPGYLVGRNNANGVDLNRNFPDLNTYIYYNEKYGGPN
HHLPLPDNWKSQVEPETRAVIRWMHSFNFVLSANLHGGAVVANYPYDKSFEHRVRGVRRT
ASTPTPDDKLFQKLAKVYSYAHGWMFQGWNCGDYFPDGITNGASWYSLSKGMQDFNYLHT
NCFEITLELSCDKFPPEEELQREWLGNREALIQFLEQVHQGIKGMVLDENYNNLANAVIS
VSGINHDVTSGDHGDYFRLLLPGIYTVSATAPGYDPETVTVTVGPAEPTLVNFHLKRSIP
QVSPVRRAPSRRHGVRAKVQPQARKKEMEMRQLQRGPA
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BDBM50275212 |
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n/a |
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Name | BDBM50275212 |
Synonyms: | CHEMBL4127473 |
Type | Small organic molecule |
Emp. Form. | C12H15ClN2O3Se |
Mol. Mass. | 349.67 |
SMILES | [#6]-[#6]-[#6](=O)[Se;v2][#6]-[#6](-[#6]-c1cnc(-[#7])c(Cl)c1)-[#6](-[#8])=O |
Structure |
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