Reaction Details |
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Target | Carbonic anhydrase |
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Ligand | BDBM10881 |
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Substrate/Competitor | BDBM10856 |
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Meas. Tech. | CA Inhibition Assay |
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Ki | 63±n/a nM |
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Citation | Innocenti, A; Hall, RA; Schlicker, C; Scozzafava, A; Steegborn, C; Mühlschlegel, FA; Supuran, CT Carbonic anhydrase inhibitors. Inhibition and homology modeling studies of the fungal beta-carbonic anhydrase from Candida albicans with sulfonamides. Bioorg Med Chem17:4503-9 (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 |
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Name: | Carbonic anhydrase |
Synonyms: | Carbonic Anhydrase 2 (Can2) |
Type: | Enzyme |
Mol. Mass.: | 26594.37 |
Organism: | Cryptococcus neoformans var. grubii (Filobasidiella neoformans var. grubii) |
Description: | n/a |
Residue: | 239 |
Sequence: | MPFHAEPLKPSDEIDMDLGHSVAAQKFKEIREVLEGNRYWARKVTSEEPEFMAEQVKGQA
PNFLWIGCADSRVPEVTIMARKPGDVFVQRNVANQFKPEDDSSQALLNYAIMNVGVTHVM
VVGHTGCGGCIAAFDQPLPTEENPGGTPLVRYLEPIIRLKHSLPEGSDVNDLIKENVKMA
VKNVVNSPTIQGAWEQARKGEFREVFVHGWLYDLSTGNIVDLNVTQGPHPFVDDRVPRA
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BDBM10881 |
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BDBM10856 |
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Name | BDBM10881 |
Synonyms: | CHEMBL288100 | MZA3 | Methazolamide | Methazolamide (MZA) | Methazolamide, MZA | N-[(2Z)-3-methyl-5-sulfamoyl-2,3-dihydro-1,3,4-thiadiazol-2-ylidene]acetamide | Sulfonamide, 2 | cid_4100 | sulfonamide 2 |
Type | Small organic molecule |
Emp. Form. | C5H8N4O3S2 |
Mol. Mass. | 236.272 |
SMILES | CC(=O)N=c1sc(nn1C)S(N)(=O)=O |w:3.2| |
Structure |
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