Reaction Details |
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Target | Carbonic anhydrase |
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Ligand | BDBM10865 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_347177 (CHEMBL862664) |
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Ki | 504±n/a nM |
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Citation | Nishimori, I; Vullo, D; Minakuchi, T; Morimoto, K; Onishi, S; Scozzafava, A; Supuran, CT Carbonic anhydrase inhibitors: cloning and sulfonamide inhibition studies of a carboxyterminal truncated alpha-carbonic anhydrase from Helicobacter pylori. Bioorg Med Chem Lett16:2182-8 (2006) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carbonic anhydrase |
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Name: | Carbonic anhydrase |
Synonyms: | Beta-carbonic anhydrase | CYNT_HELPY | Carbonic anhydrase 1 | cynT | hpβCA |
Type: | Protein |
Mol. Mass.: | 25517.77 |
Organism: | Helicobacter pylori (strain G27) |
Description: | O24855 |
Residue: | 221 |
Sequence: | MKAFLGALEFQENEYEELKELYESLKTKQKPHTLFISCVDSRVVPNLITGTKPGELYVIC
NMGNVNPPKTSYKESLSTIASIEYAIAHVGVQNLIICGHSDCGACGSVHLIHDETTKAKT
PYIANWIQFLEPVKEELKNHPQFSNHFAKRSWLTERLNARLQLNNLLSYDFIQEKASKNE
LKIFGWHYIIETGRIYNYNFESHFFEPIGETIKQRKSHENF
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BDBM10865 |
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n/a |
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Name | BDBM10865 |
Synonyms: | 4-Amino-3-iodobenzenesulfonamide | 4-amino-3-iodobenzene-1-sulfonamide | CHEMBL268177 | aromatic/heteroaromatic sulfonamide 10 | halogenosulfanilamide deriv. 5e |
Type | Small organic molecule |
Emp. Form. | C6H7IN2O2S |
Mol. Mass. | 298.101 |
SMILES | Nc1ccc(cc1I)S(N)(=O)=O |
Structure |
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