Reaction Details |
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Target | CARBONIC ANHYDRASE |
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Ligand | BDBM10863 |
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Substrate/Competitor | BDBM10856 |
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Meas. Tech. | CA Inhibition Assay |
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Ki | 378±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 |
Synonyms: | Carbonic Anhydrase (hpCA) | hpCA |
Type: | Enzyme |
Mol. Mass.: | 28277.52 |
Organism: | Helicobacter pylori J99 |
Description: | Q9ZK30 |
Residue: | 247 |
Sequence: | MKKTFLIALALTASLIGAENTKWDYKNKENGPHRWDKLHKDFEVCKSGKSQSPINIEHYY
HTQDKADLQFKYAASKPKAVFFTHHTLKASFEPTNHINYRGHDYVLDNVHFHAPMEFLIN
NKTRPLSAHFVHKDAKGRLLVLAIGFEEGKENPNLDPILEGIQKKQNLKEVALDAFLPKS
INYYHFNGSLTAPPCTEGVAWFVIEEPLEVSAKQLAEIKKRMKNSPNQRPVQPDYNTVII
KSSAETR
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BDBM10863 |
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BDBM10856 |
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Name | BDBM10863 |
Synonyms: | 4-Amino-3-chlorobenzenesulfonamide | 4-amino-3-chlorobenzene-1-sulfonamide | CHEMBL7092 | aromatic/heteroaromatic sulfonamide 8 | halogenosulfanilamide deriv. 5c |
Type | Small organic molecule |
Emp. Form. | C6H7ClN2O2S |
Mol. Mass. | 206.65 |
SMILES | Nc1ccc(cc1Cl)S(N)(=O)=O |
Structure |
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