Reaction Details |
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Target | Carbonic anhydrase 7 |
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Ligand | BDBM50208750 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_443319 (CHEMBL893567) |
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Ki | 25±n/a nM |
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Citation | Winum, JY; Thiry, A; Cheikh, KE; Dogné, JM; Montero, JL; Vullo, D; Scozzafava, A; Masereel, B; Supuran, CT Carbonic anhydrase inhibitors. Inhibition of isoforms I, II, IV, VA, VII, IX, and XIV with sulfonamides incorporating fructopyranose-thioureido tails. Bioorg Med Chem Lett17:2685-91 (2007) [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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BDBM50208750 |
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n/a |
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Name | BDBM50208750 |
Synonyms: | 1-{2-fluoro-4-[(5-sulfamoyl-1,3,4-thiadiazol-2-yl)sulfamoyl]phenyl}-3-{[(1R,2S,6S,9R)-4,4,11,11-tetramethyl-3,5,7,10,12-pentaoxatricyclo[7.3.0.0^{2,6}]dodecan-6-yl]methyl}thiourea | CHEMBL395981 |
Type | Small organic molecule |
Emp. Form. | C21H27FN6O9S4 |
Mol. Mass. | 654.732 |
SMILES | CC1(C)O[C@@H]2CO[C@@]3(CNC(=S)Nc4ccc(cc4F)S(=O)(=O)Nc4nnc(s4)S(N)(=O)=O)OC(C)(C)O[C@H]3[C@@H]2O1 |
Structure |
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