Reaction Details |
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Target | Carbonic anhydrase 1 |
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Ligand | BDBM50084540 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_47511 (CHEMBL657821) |
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Ki | 10±n/a nM |
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Citation | Scozzafava, A; Briganti, F; Ilies, MA; Supuran, CT Carbonic anhydrase inhibitors: synthesis of membrane-impermeant low molecular weight sulfonamides possessing in vivo selectivity for the membrane-bound versus cytosolic isozymes. J Med Chem43:292-300 (2000) [PubMed] |
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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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BDBM50084540 |
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n/a |
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Name | BDBM50084540 |
Synonyms: | 2,6-Dimethyl-4-phenyl-1-[(2-sulfamoyl-benzothiazol-6-ylcarbamoyl)-methyl]-pyridinium; perchlorate | CHEMBL421200 |
Type | Small organic molecule |
Emp. Form. | C22H21N4O3S2 |
Mol. Mass. | 453.557 |
SMILES | Cc1cc(cc(C)[n+]1CC(=O)Nc1ccc2nc(sc2c1)S(N)(=O)=O)-c1ccccc1 |
Structure |
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