Reaction Details |
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Target | beta-Carbonic Anhydrase |
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Ligand | BDBM10864 |
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Substrate/Competitor | BDBM10856 |
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Meas. Tech. | CA Inhibition Assay |
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pH | 8.3±n/a |
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Temperature | 293.15±n/a K |
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Ki | 408±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 Chem 17:4503-9 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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beta-Carbonic Anhydrase |
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Name: | beta-Carbonic Anhydrase |
Synonyms: | NCE103 |
Type: | Enzyme |
Mol. Mass.: | 31587.59 |
Organism: | Candida albicans (Yeast) |
Description: | n/a |
Residue: | 281 |
Sequence: | MGRENILKYQLEHDHESDLVTEKDQSLLLDNNNNLNGMNNTIKTHPVRVSSGNHNNFPFT
LSSESTLQDFLNNNKFFVDSIKHNHGNQIFDLNGQGQSPHTLWIGCSDSRAGDQCLATLP
GEIFVHRNIANIVNANDISSQGVIQFAIDVLKVKKIIVCGHTDCGGIWASLSKKKIGGVL
DLWLNPVRHIRAANLKLLEEYNQDPKLKAKKLAELNVISSVTALKRHPSASVALKKNEIE
VWGMLYDVATGYLSQVEIPQDEFEDLFHVHDEHDEEEYNPH
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BDBM10864 |
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BDBM10856 |
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Name | BDBM10864 |
Synonyms: | 4-Amino-3-bromobenzenesulfonamide | 4-amino-3-bromobenzene-1-sulfonamide | CHEMBL6724 | aromatic/heteroaromatic sulfonamide 9 | halogenosulfanilamide deriv. 5d |
Type | Small organic molecule |
Emp. Form. | C6H7BrN2O2S |
Mol. Mass. | 251.101 |
SMILES | Nc1ccc(cc1Br)S(N)(=O)=O |
Structure |
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