Reaction Details |
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Target | Carbonic anhydrase 1 |
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Ligand | BDBM50163863 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1673905 (CHEMBL4023934) |
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KOFF | 0.0075 s-1 |
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Citation | Linkuvien?, V; Talibov, VO; Danielson, UH; Matulis, D Introduction of Intrinsic Kinetics of Protein-Ligand Interactions and Their Implications for Drug Design. J Med Chem61:2292-2302 (2018) [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: | 4.2.1.1 | CA-I | CA1 | CAH1_MACMU | Carbonate dehydratase I | Carbonic anhydrase 1 | Carbonic anhydrase I |
Type: | PROTEIN |
Mol. Mass.: | 28941.00 |
Organism: | Macaca mulatta |
Description: | ChEMBL_117334 |
Residue: | 261 |
Sequence: | MASPDWGYDDKNGPEQWSKLYPIANGNNQSPVDIKTSEAKHDTSLKPISVSYNPATAKEI
INVGHSFHVNFEDNDNRSVLKGGPFSDSYRLFQFHFHWGSSNEYGSEHTVDGVKYSSELH
IVHWNSAKYSSLAEAVSKADGLAVIGVLMKVGEANPKLQKVLDALHAIKTKGKRAPFTNF
DPSTLLPSSLDFWTYSGSLTHPPLYESVTWIICKESISVSSEQLAQFRSLLSNVEGSNPV
PIQRNNRPTQPLKGRTVRASF
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BDBM50163863 |
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n/a |
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Name | BDBM50163863 |
Synonyms: | 4-(1H-benzimidazol-1-ylacetyl)-2-chlorobenzenesulfonamide (2a) | CHEMBL3798446 | carbonic anhydrase (CA) inhibitors, benzenesulphonamide ligand, 2 |
Type | Small organic molecule |
Emp. Form. | C15H12ClN3O3S |
Mol. Mass. | 349.792 |
SMILES | NS(=O)(=O)c1ccc(cc1Cl)C(=O)Cn1cnc2ccccc12 |
Structure |
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