Reaction Details |
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Target | Carboxypeptidase B |
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Ligand | BDBM50296422 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_580862 (CHEMBL1064194) |
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Ki | 11700±n/a nM |
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Citation | Fernández, D; Avilés, FX; Vendrell, J A new type of five-membered heterocyclic inhibitors of basic metallocarboxypeptidases. Eur J Med Chem44:3266-71 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carboxypeptidase B |
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Name: | Carboxypeptidase B |
Synonyms: | CBPB1_HUMAN | CPB | CPB1 | Carboxypeptidase B | PASP | PCPB | Pancreas-specific protein | Thrombin-activatable fibrinolysis (TAFI) |
Type: | Enzyme |
Mol. Mass.: | 47367.43 |
Organism: | Homo sapiens (Human) |
Description: | P15086 |
Residue: | 417 |
Sequence: | MLALLVLVTVALASAHHGGEHFEGEKVFRVNVEDENHINIIRELASTTQIDFWKPDSVTQ
IKPHSTVDFRVKAEDTVTVENVLKQNELQYKVLISNLRNVVEAQFDSRVRATGHSYEKYN
KWETIEAWTQQVATENPALISRSVIGTTFEGRAIYLLKVGKAGQNKPAIFMDCGFHAREW
ISPAFCQWFVREAVRTYGREIQVTELLDKLDFYVLPVLNIDGYIYTWTKSRFWRKTRSTH
TGSSCIGTDPNRNFDAGWCEIGASRNPCDETYCGPAAESEKETKALADFIRNKLSSIKAY
LTIHSYSQMMIYPYSYAYKLGENNAELNALAKATVKELASLHGTKYTYGPGATTIYPAAG
GSDDWAYDQGIRYSFTFELRDTGRYGFLLPESQIRATCEETFLAIKYVASYVLEHLY
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BDBM50296422 |
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n/a |
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Name | BDBM50296422 |
Synonyms: | 2-(5-((4-chlorophenoxy)methyl)-1,3,4-oxadiazol-2-ylthio)-1-p-tolylethanone | CHEMBL562891 |
Type | Small organic molecule |
Emp. Form. | C18H15ClN2O3S |
Mol. Mass. | 374.841 |
SMILES | Cc1ccc(cc1)C(=O)CSc1nnc(COc2ccc(Cl)cc2)o1 |
Structure |
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