Reaction Details |
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Target | Carboxypeptidase B2 |
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Ligand | BDBM50144323 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_206146 |
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IC50 | 1500±n/a nM |
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Citation | Nantermet, PG; Barrow, JC; Lindsley, SR; Young, M; Mao, SS; Carroll, S; Bailey, C; Bosserman, M; Colussi, D; McMasters, DR; Vacca, JP; Selnick, HG Imidazole acetic acid TAFIa inhibitors: SAR studies centered around the basic P(1)(') group. Bioorg Med Chem Lett14:2141-5 (2004) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carboxypeptidase B2 |
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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: | MKLCSLAVLVPIVLFCEQHVFAFQSGQVLAALPRTSRQVQVLQNLTTTYEIVLWQPVTAD
LIVKKKQVHFFVNASDVDNVKAHLNVSGIPCSVLLADVEDLIQQQISNDTVSPRASASYY
EQYHSLNEIYSWIEFITERHPDMLTKIHIGSSFEKYPLYVLKVSGKEQAAKNAIWIDCGI
HAREWISPAFCLWFIGHITQFYGIIGQYTNLLRLVDFYVMPVVNVDGYDYSWKKNRMWRK
NRSFYANNHCIGTDLNRNFASKHWCEEGASSSSCSETYCGLYPESEPEVKAVASFLRRNI
NQIKAYISMHSYSQHIVFPYSYTRSKSKDHEELSLVASEAVRAIEKISKNTRYTHGHGSE
TLYLAPGGGDDWIYDLGIKYSFTIELRDTGTYGFLLPERYIKPTCREAFAAVSKIAWHVI
RNV
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BDBM50144323 |
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n/a |
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Name | BDBM50144323 |
Synonyms: | 3-(6-Amino-4-methyl-pyridin-3-yl)-2-(1H-imidazol-4-yl)-propionic acid | CHEMBL304532 |
Type | Small organic molecule |
Emp. Form. | C12H14N4O2 |
Mol. Mass. | 246.2652 |
SMILES | Cc1cc(N)ncc1CC(C(O)=O)c1cnc[nH]1 |
Structure |
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