Reaction Details |
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Target | Carbonic anhydrase 6 |
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Ligand | BDBM50137676 |
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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 | 3.4±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 6 |
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Name: | Carbonic anhydrase 6 |
Synonyms: | CA-VI | CA6 | CAH6_HUMAN | Carbonate dehydratase VI | Carbonic Anhydrase VI | Carbonic anhydrase | Carbonic anhydrase 6 | Carbonic anhydrase 6 (CA VI) | Carbonic anhydrase 6 (CA-VI) | Carbonic anhydrase VI (CA VI) | Salivary carbonic anhydrase | Secreted carbonic anhydrase |
Type: | Enzyme |
Mol. Mass.: | 35371.40 |
Organism: | Homo sapiens (Human) |
Description: | P23280 |
Residue: | 308 |
Sequence: | MRALVLLLSLFLLGGQAQHVSDWTYSEGALDEAHWPQHYPACGGQRQSPINLQRTKVRYN
PSLKGLNMTGYETQAGEFPMVNNGHTVQISLPSTMRMTVADGTVYIAQQMHFHWGGASSE
ISGSEHTVDGIRHVIEIHIVHYNSKYKSYDIAQDAPDGLAVLAAFVEVKNYPENTYYSNF
ISHLANIKYPGQRTTLTGLDVQDMLPRNLQHYYTYHGSLTTPPCTENVHWFVLADFVKLS
RTQVWKLENSLLDHRNKTIHNDYRRTQPLNHRVVESNFPNQEYTLGSEFQFYLHKIEEIL
DYLRRALN
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BDBM50137676 |
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n/a |
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Name | BDBM50137676 |
Synonyms: | 4-(3,4,5-Trihydroxy-6-methyl-tetrahydro-pyran-2-ylamino)-benzenesulfonamide | CHEMBL74846 | N-(p-sulfamoylphenyl)-alpha-glycopyranosylamine, 7 | N-(p-sulfamoylphenyl)-alpha-glycopyranosylamine, 8 |
Type | Small organic molecule |
Emp. Form. | C12H18N2O6S |
Mol. Mass. | 318.346 |
SMILES | CC1OC(Nc2ccc(cc2)S(N)(=O)=O)C(O)C(O)C1O |
Structure |
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