Reaction Details |
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Target | Carbonic anhydrase 7 |
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Ligand | BDBM50329832 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1572869 (CHEMBL3801005) |
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KOFF | 0.27 s-1 |
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Citation | Talibov, VO; Linkuviene, V; Matulis, D; Danielson, UH Kinetically Selective Inhibitors of Human Carbonic Anhydrase Isozymes I, II, VII, IX, XII, and XIII. J Med Chem59:2083-93 (2016) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carbonic anhydrase 7 |
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Name: | Carbonic anhydrase 7 |
Synonyms: | CA-VII | CA7 | CAH7_HUMAN | Carbonate dehydratase VII | Carbonic anhydrase | Carbonic anhydrase VII | Carbonic anhydrase VII (CA VII) |
Type: | Enzyme |
Mol. Mass.: | 29664.11 |
Organism: | Homo sapiens (Human) |
Description: | Human cloned isozyme. |
Residue: | 264 |
Sequence: | MTGHHGWGYGQDDGPSHWHKLYPIAQGDRQSPINIISSQAVYSPSLQPLELSYEACMSLS
ITNNGHSVQVDFNDSDDRTVVTGGPLEGPYRLKQFHFHWGKKHDVGSEHTVDGKSFPSEL
HLVHWNAKKYSTFGEAASAPDGLAVVGVFLETGDEHPSMNRLTDALYMVRFKGTKAQFSC
FNPKCLLPASRHYWTYPGSLTTPPLSESVTWIVLREPICISERQMGKFRSLLFTSEDDER
IHMVNNFRPPQPLKGRVVKASFRA
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BDBM50329832 |
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n/a |
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Name | BDBM50329832 |
Synonyms: | 5-(1H-Benzimidazol-1-ylacetyl)-2-chlorobenzenesulfonamide | CHEMBL1272187 | N-alkylated benzimidazole derivative, 4a | carbonic anhydrase (CA) inhibitors, benzenesulphonamide ligand, 4 |
Type | Small organic molecule |
Emp. Form. | C15H12ClN3O3S |
Mol. Mass. | 349.792 |
SMILES | NS(=O)(=O)c1cc(ccc1Cl)C(=O)Cn1cnc2ccccc12 |
Structure |
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