Reaction Details |
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Target | Carbonic anhydrase 12 |
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Ligand | BDBM50133409 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1525821 (CHEMBL3635735) |
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Ki | 8.1±n/a nM |
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Citation | La Regina, G; Coluccia, A; Famiglini, V; Pelliccia, S; Monti, L; Vullo, D; Nuti, E; Alterio, V; De Simone, G; Monti, SM; Pan, P; Parkkila, S; Supuran, CT; Rossello, A; Silvestri, R Discovery of 1,1'-Biphenyl-4-sulfonamides as a New Class of Potent and Selective Carbonic Anhydrase XIV Inhibitors. J Med Chem58:8564-72 (2015) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carbonic anhydrase 12 |
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Name: | Carbonic anhydrase 12 |
Synonyms: | CA-XII | CA12 | CAH12_HUMAN | Carbonate dehydratase XII | Carbonic anhydrase | Carbonic anhydrase 12 (CA XII) | Carbonic anhydrase XII | Carbonic anhydrase XII (CA XII) | Carbonic anhydrase XII (CAXII) | Tumor antigen HOM-RCC-3.1.3 |
Type: | Enzyme |
Mol. Mass.: | 39456.00 |
Organism: | Homo sapiens (Human) |
Description: | Catalytic domain of human cloned isozyme was used in the assay |
Residue: | 354 |
Sequence: | MPRRSLHAAAVLLLVILKEQPSSPAPVNGSKWTYFGPDGENSWSKKYPSCGGLLQSPIDL
HSDILQYDASLTPLEFQGYNLSANKQFLLTNNGHSVKLNLPSDMHIQGLQSRYSATQLHL
HWGNPNDPHGSEHTVSGQHFAAELHIVHYNSDLYPDASTASNKSEGLAVLAVLIEMGSFN
PSYDKIFSHLQHVKYKGQEAFVPGFNIEELLPERTAEYYRYRGSLTTPPCNPTVLWTVFR
NPVQISQEQLLALETALYCTHMDDPSPREMINNFRQVQKFDERLVYTSFSQVQVCTAAGL
SLGIILSLALAGILGICIVVVVSIWLFRRKSIKKGDNKGVIYKPATKMETEAHA
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BDBM50133409 |
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n/a |
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Name | BDBM50133409 |
Synonyms: | CHEMBL3632845 |
Type | Small organic molecule |
Emp. Form. | C19H18N2O2S |
Mol. Mass. | 338.423 |
SMILES | Nc1ccc(Cc2ccc(cc2)-c2ccc(cc2)S(N)(=O)=O)cc1 |
Structure |
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