Reaction Details |
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Target | CARBONIC ANHYDRASE |
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Ligand | BDBM10896 |
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Substrate/Competitor | BDBM10856 |
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Meas. Tech. | CA Inhibition Assay |
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Ki | 13±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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BDBM10896 |
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BDBM10856 |
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Name | BDBM10896 |
Synonyms: | 4-tert-butyl-N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)benzamide | 5-(4-tert-Butylphenylcarboxamido)-1,3,4-thiadiazole-2-sulfonamide | aromatic/heteroaromatic sulfonamide 30 |
Type | Small organic molecule |
Emp. Form. | C13H16N4O3S2 |
Mol. Mass. | 340.421 |
SMILES | CC(C)(C)c1ccc(cc1)C(=O)Nc1nnc(s1)S(N)(=O)=O |
Structure |
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