Reaction Details |
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Target | Carbonic anhydrase 1 |
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Ligand | BDBM50326107 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_659850 (CHEMBL1246740) |
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Ki | 14200±n/a nM |
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Citation | Brzozowski, Z; Slawinski, J; Innocenti, A; Supuran, CT Carbonic anhydrase inhibitors. Regioselective synthesis of novel 1-substituted 1,4-dihydro-4-oxo-3-pyridinesulfonamides and their inhibition of the human cytosolic isozymes I and II and transmembrane cancer-associated isozymes IX and XII. Eur J Med Chem45:3656-61 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carbonic anhydrase 1 |
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Name: | Carbonic anhydrase 1 |
Synonyms: | CA-I | CA1 | CAB | CAH1_HUMAN | Carbonate dehydratase I | Carbonic anhydrase | Carbonic anhydrase 1 (CA I) | Carbonic anhydrase 1 (CA-I) | Carbonic anhydrase 1 (Recombinant CA I) | Carbonic anhydrase 2 (CA II) | Carbonic anhydrase B | Carbonic anhydrase I | Carbonic anhydrase I (CA I) | Carbonic anhydrase I (CA-I) | Carbonic anhydrase I (CAI) | Carbonic anhydrase I (hCA I) | Carbonic anhydrase isoenzyme I (hCA I) | hCA |
Type: | Enzyme |
Mol. Mass.: | 28873.37 |
Organism: | Homo sapiens (Human) |
Description: | P00915 |
Residue: | 261 |
Sequence: | MASPDWGYDDKNGPEQWSKLYPIANGNNQSPVDIKTSETKHDTSLKPISVSYNPATAKEI
INVGHSFHVNFEDNDNRSVLKGGPFSDSYRLFQFHFHWGSTNEHGSEHTVDGVKYSAELH
VAHWNSAKYSSLAEAASKADGLAVIGVLMKVGEANPKLQKVLDALQAIKTKGKRAPFTNF
DPSTLLPSSLDFWTYPGSLTHPPLYESVTWIICKESISVSSEQLAQFRSLLSNVEGDNAV
PMQHNNRPTQPLKGRTVRASF
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BDBM50326107 |
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n/a |
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Name | BDBM50326107 |
Synonyms: | 1,4-Dihydro-1-(2-naphthoylmethyl)-4-oxo-3-pyridinesulfonamide | CHEMBL1242794 |
Type | Small organic molecule |
Emp. Form. | C17H14N2O4S |
Mol. Mass. | 342.369 |
SMILES | NS(=O)(=O)c1cn(CC(=O)c2ccc3ccccc3c2)ccc1=O |
Structure |
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