Reaction Details |
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Target | Carbonic anhydrase 12 |
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Ligand | BDBM50320512 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_637718 (CHEMBL1167309) |
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Ki | 15.7±n/a nM |
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Citation | Brzozowski, Z; Slawinski, J; Saczewski, F; Innocenti, A; Supuran, CT Carbonic anhydrase inhibitors: synthesis and inhibition of the human cytosolic isozymes I and II and transmembrane isozymes IX, XII (cancer-associated) and XIV with 4-substituted 3-pyridinesulfonamides. Eur J Med Chem45:2396-404 (2010) [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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BDBM50320512 |
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n/a |
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Name | BDBM50320512 |
Synonyms: | 4-(5-Methyl-2-pirazolino)-3-pyridinesulfonamide | CHEMBL1163382 |
Type | Small organic molecule |
Emp. Form. | C9H12N4O2S |
Mol. Mass. | 240.282 |
SMILES | CC1CC=NN1c1ccncc1S(N)(=O)=O |c:3| |
Structure |
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