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Sulfonylureas have antifungal activity and are potent inhibitors of Candida albicans acetohydroxyacid synthase.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2013 Jan 10; Vol. 56 (1), pp. 210-9. Date of Electronic Publication: 2012 Dec 31. - Publication Year :
- 2013
-
Abstract
- The sulfonylurea herbicides exert their activity by inhibiting plant acetohydroxyacid synthase (AHAS), the first enzyme in the branched-chain amino acid biosynthesis pathway. It has previously been shown that if the gene for AHAS is deleted in Candida albicans , attenuation of virulence is achieved, suggesting AHAS as an antifungal drug target. Herein, we have cloned, expressed, and purified C. albicans AHAS and shown that several sulfonylureas are inhibitors of this enzyme and possess antifungal activity. The most potent of these compounds is ethyl 2-(N-((4-iodo-6-methoxypyrimidin-2-yl)carbamoyl)sulfamoyl)benzoate (10c), which has a K(i) value of 3.8 nM for C. albicans AHAS and an MIC₉₀ of 0.7 μg/mL for this fungus in cell-based assays. For the sulfonylureas tested there was a strong correlation between inhibitory activity toward C. albicans AHAS and fungicidal activity, supporting the hypothesis that AHAS is the target for their inhibitory activity within the cell.
- Subjects :
- Acetolactate Synthase chemistry
Amino Acid Sequence
Antifungal Agents chemistry
Antifungal Agents pharmacology
Benzoates chemistry
Benzoates pharmacology
Candida albicans enzymology
Catalytic Domain
Disk Diffusion Antimicrobial Tests
Herbicides pharmacology
Microbial Sensitivity Tests
Models, Molecular
Molecular Sequence Data
Recombinant Proteins antagonists & inhibitors
Recombinant Proteins chemistry
Structure-Activity Relationship
Sulfonylurea Compounds chemistry
Sulfonylurea Compounds pharmacology
Acetolactate Synthase antagonists & inhibitors
Antifungal Agents chemical synthesis
Benzoates chemical synthesis
Candida albicans drug effects
Sulfonylurea Compounds chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4804
- Volume :
- 56
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 23237384
- Full Text :
- https://doi.org/10.1021/jm301501k