Reaction Details |
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Target | Carbonic anhydrase 2 |
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Ligand | BDBM50043905 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_45049 (CHEMBL658047) |
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Ki | 11±n/a nM |
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Citation | Hunt, CA; Mallorga, PJ; Michelson, SR; Schwam, H; Sondey, JM; Smith, RL; Sugrue, MF; Shepard, KL 3-substituted thieno[2,3-b][1,4]thiazine-6-sulfonamides. A novel class of topically active carbonic anhydrase inhibitors. J Med Chem37:240-7 (1994) [PubMed] |
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More Info.: | Get all data from this article, 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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BDBM50043905 |
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n/a |
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Name | BDBM50043905 |
Synonyms: | CHEMBL79368 | N-Isobutyl-2-(2-oxo-6-sulfamoyl-2,3-dihydro-1H-thieno[2,3-b][1,4]thiazin-3-yl)-acetamide |
Type | Small organic molecule |
Emp. Form. | C8H10N2O4S3 |
Mol. Mass. | 294.371 |
SMILES | NS(=O)(=O)c1cc2NCC3(CC3)S(=O)(=O)c2s1 |
Structure |
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