Reaction Details |
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Target | Carbonic anhydrase 13 |
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Ligand | BDBM10862 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_45453 |
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Ki | 50±n/a nM |
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Citation | Lehtonen, JM; Parkkila, S; Vullo, D; Casini, A; Scozzafava, A; Supuran, CT Carbonic anhydrase inhibitors. Inhibition of cytosolic isozyme XIII with aromatic and heterocyclic sulfonamides: a novel target for the drug design. Bioorg Med Chem Lett14:3757-62 (2004) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carbonic anhydrase 13 |
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Name: | Carbonic anhydrase 13 |
Synonyms: | CA-XIII | CAH13_MOUSE | Ca13 | Car13 | Carbonate dehydratase XIII | Carbonic anhydrase 13 | Carbonic anhydrase XIII |
Type: | Enzyme |
Mol. Mass.: | 29522.80 |
Organism: | Mus musculus (mouse) |
Description: | Murine cloned isozyme |
Residue: | 262 |
Sequence: | MARLSWGYGEHNGPIHWNELFPIADGDQQSPIEIKTKEVKYDSSLRPLSIKYDPASAKII
SNSGHSFNVDFDDTEDKSVLRGGPLTGNYRLRQFHLHWGSADDHGSEHVVDGVRYAAELH
VVHWNSDKYPSFVEAAHESDGLAVLGVFLQIGEHNPQLQKITDILDSIKEKGKQTRFTNF
DPLCLLPSSWDYWTYPGSLTVPPLLESVTWIVLKQPISISSQQLARFRSLLCTAEGESAA
FLLSNHRPPQPLKGRRVRASFY
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BDBM10862 |
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n/a |
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Name | BDBM10862 |
Synonyms: | 4-Amino-3-fluorobenzenesulfonamide | 4-amino-3-fluorobenzene-1-sulfonamide | CHEMBL6853 | aromatic/heteroaromatic sulfonamide 7 | halogenosulfanilamide deriv. 5b |
Type | Small organic molecule |
Emp. Form. | C6H7FN2O2S |
Mol. Mass. | 190.195 |
SMILES | Nc1ccc(cc1F)S(N)(=O)=O |
Structure |
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