| Reaction Details |
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 | Report a problem with these data |
| Target | CARBONIC ANHYDRASE |
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| Ligand | BDBM10875 |
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| Substrate/Competitor | BDBM10856 |
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| Meas. Tech. | CA Inhibition Assay |
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| Ki | 105±n/a nM |
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| Citation |  Nishimori, I; Minakuchi, T; Morimoto, K; Sano, S; Onishi, S; Takeuchi, H; Vullo, D; Scozzafava, A; Supuran, CT Carbonic anhydrase inhibitors: DNA cloning and inhibition studies of the alpha-carbonic anhydrase from Helicobacter pylori, a new target for developing sulfonamide and sulfamate gastric drugs. J Med Chem49:2117-26 (2006) [PubMed] Article |
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| More Info.: | Get all data from this article, Solution Info, Assay Method |
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| CARBONIC ANHYDRASE |
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| Name: | CARBONIC ANHYDRASE |
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| Synonyms: | Carbonic Anhydrase (hpCA) | hpCA |
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| Type: | Enzyme |
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| Mol. Mass.: | 28277.52 |
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| Organism: | Helicobacter pylori J99 |
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| Description: | Q9ZK30 |
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| Residue: | 247 |
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| Sequence: | MKKTFLIALALTASLIGAENTKWDYKNKENGPHRWDKLHKDFEVCKSGKSQSPINIEHYY
HTQDKADLQFKYAASKPKAVFFTHHTLKASFEPTNHINYRGHDYVLDNVHFHAPMEFLIN
NKTRPLSAHFVHKDAKGRLLVLAIGFEEGKENPNLDPILEGIQKKQNLKEVALDAFLPKS
INYYHFNGSLTAPPCTEGVAWFVIEEPLEVSAKQLAEIKKRMKNSPNQRPVQPDYNTVII
KSSAETR
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| BDBM10875 |
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| BDBM10856 |
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| Name | BDBM10875 |
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| Synonyms: | 5-(2-chlorophenyl)-1,3,4-thiadiazole-2-sulfonamide | CHEMBL360356 | Chlorzolamide, CHL | JMC522226 Compound 19 | JMC523116 Compound 19 | aromatic/heteroaromatic sulfonamide 20 |
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| Type | Small organic molecule |
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| Emp. Form. | C8H6ClN3O2S2 |
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| Mol. Mass. | 275.735 |
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| SMILES | NS(=O)(=O)c1nnc(s1)-c1ccccc1Cl |
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| Structure | 
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