Reaction Details |
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Target | Carbonic anhydrase 7 |
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Ligand | BDBM50380148 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_811726 (CHEMBL2014301) |
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Kd | 83±n/a nM |
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Citation | Capkauskaite, E; Zubriene, A; Baranauskiene, L; Tamulaitiene, G; Manakova, E; Kairys, V; Gražulis, S; Tumkevicius, S; Matulis, D Design of [(2-pyrimidinylthio)acetyl]benzenesulfonamides as inhibitors of human carbonic anhydrases. Eur J Med Chem51:259-70 (2012) [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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BDBM50380148 |
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n/a |
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Name | BDBM50380148 |
Synonyms: | CHEMBL2011156 | carbonic anhydrase (CA) inhibitors, benzenesulphonamide ligand, 6 |
Type | Small organic molecule |
Emp. Form. | C12H11N3O3S2 |
Mol. Mass. | 309.364 |
SMILES | NS(=O)(=O)c1ccc(cc1)C(=O)CSc1ncccn1 |
Structure |
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