Reaction Details |
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Target | Carboxypeptidase M |
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Ligand | BDBM50121929 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_45790 (CHEMBL660086) |
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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 M |
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Name: | Carboxypeptidase M |
Synonyms: | CBPM_HUMAN | CPM |
Type: | PROTEIN |
Mol. Mass.: | 50519.81 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_45790 |
Residue: | 443 |
Sequence: | MDFPCLWLGLLLPLVAALDFNYHRQEGMEAFLKTVAQNYSSVTHLHSIGKSVKGRNLWVL
VVGRFPKEHRIGIPEFKYVANMHGDETVGRELLLHLIDYLVTSDGKDPEITNLINSTRIH
IMPSMNPDGFEAVKKPDCYYSIGRENYNQYDLNRNFPDAFEYNNVSRQPETVAVMKWLKT
ETFVLSANLHGGALVASYPFDNGVQATGALYSRSLTPDDDVFQYLAHTYASRNPNMKKGD
ECKNKMNFPNGVTNGYSWYPLQGGMQDYNYIWAQCFEITLELSCCKYPREEKLPSFWNNN
KASLIEYIKQVHLGVKGQVFDQNGNPLPNVIVEVQDRKHICPYRTNKYGEYYLLLLPGSY
IINVTVPGHDPHITKVIIPEKSQNFSALKKDILLPFQGQLDSIPVSNPSCPMIPLYRNLP
DHSAATKPSLFLFLVSLLHIFFK
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BDBM50121929 |
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n/a |
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Name | BDBM50121929 |
Synonyms: | (phenylmethyl)butanedioic acid | 2-benzylbutanedioic acid | 2-benzylsuccinic acid | CHEMBL151284 | alpha-benzylsuccinic acid | benzylsuccinic acid | beta-carboxybenzenebutanoic acid |
Type | Small organic molecule |
Emp. Form. | C11H12O4 |
Mol. Mass. | 208.2106 |
SMILES | OC(=O)CC(Cc1ccccc1)C(O)=O |
Structure |
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