Reaction Details |
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Target | Carbonic anhydrase 2 |
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Ligand | BDBM50137677 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Enzyme Inhbition Assay |
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pH | 7.5±0 |
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Temperature | 293.15±0 K |
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Ki | 25±0.0 nM |
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Citation | Winum, JY; Montero, JL; Vullo, D; Supuran, CT Carbonic anhydrase inhibitors: glycosylsulfanilamides act as subnanomolar inhibitors of the human secreted isoform VI. Chem Biol Drug Des74:636-9 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Carbonic anhydrase 2 |
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Name: | Carbonic anhydrase 2 |
Synonyms: | CA-II | CA2 | CAC | CAH2_HUMAN | Carbonate dehydratase II | Carbonic anhydrase 2 (CA II) | Carbonic anhydrase 2 (CA-II) | Carbonic anhydrase 2 (Recombinant CA II) | Carbonic anhydrase C | Carbonic anhydrase II (CA II) | Carbonic anhydrase II (CA-II) | Carbonic anhydrase II (CAII) | Carbonic anhydrase II (hCA II) | Carbonic anhydrase isoenzyme II (hCA II) |
Type: | Enzyme |
Mol. Mass.: | 29250.71 |
Organism: | Homo sapiens (Human) |
Description: | P00918 |
Residue: | 260 |
Sequence: | MSHHWGYGKHNGPEHWHKDFPIAKGERQSPVDIDTHTAKYDPSLKPLSVSYDQATSLRIL
NNGHAFNVEFDDSQDKAVLKGGPLDGTYRLIQFHFHWGSLDGQGSEHTVDKKKYAAELHL
VHWNTKYGDFGKAVQQPDGLAVLGIFLKVGSAKPGLQKVVDVLDSIKTKGKSADFTNFDP
RGLLPESLDYWTYPGSLTTPPLLECVTWIVLKEPISVSSEQVLKFRKLNFNGEGEPEELM
VDNWRPAQPLKNRQIKASFK
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BDBM50137677 |
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n/a |
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Name | BDBM50137677 |
Synonyms: | 4-(3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-ylamino)-benzenesulfonamide | CHEMBL72447 | N-(p-sulfamoylphenyl)-alpha-glycopyranosylamine, 1 | N-(p-sulfamoylphenyl)-alpha-glycopyranosylamine, 2 | N-(p-sulfamoylphenyl)-alpha-glycopyranosylamine, 3 |
Type | Small organic molecule |
Emp. Form. | C12H18N2O7S |
Mol. Mass. | 334.346 |
SMILES | NS(=O)(=O)c1ccc(NC2OC(CO)C(O)C(O)C2O)cc1 |
Structure |
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