Reaction Details |
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Target | Carboxypeptidase B |
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Ligand | BDBM50296423 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_580862 (CHEMBL1064194) |
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Ki | 16600±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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BDBM50296423 |
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n/a |
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Name | BDBM50296423 |
Synonyms: | CHEMBL551672 | N-(2-chlorobenzyl)-N-(furan-2-ylmethyl)-3-methyl-4-(1H-tetrazol-1-yl)benzenesulfonamide |
Type | Small organic molecule |
Emp. Form. | C20H18ClN5O3S |
Mol. Mass. | 443.907 |
SMILES | Cc1cc(ccc1-n1cnnn1)S(=O)(=O)N(Cc1ccco1)Cc1ccccc1Cl |
Structure |
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