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- W4200241342 endingPage "112523" @default.
- W4200241342 startingPage "112523" @default.
- W4200241342 abstract "Four types of antifungal drugs are available that include inhibitors of ergosterol synthesis, of fungal RNA biosynthesis, and of cell wall biosynthesis as well as physiochemical regulators of fungal membrane sterols. Increasing resistance to antifungal drugs can severely limit treatment options of fungal nail infections, vaginal candidiasis, ringworm, blastomycosis, histoplasmosis, and Candida infections of the mouth, throat, and esophagus, among other infections. Development of strategies focused on new fungicides can effectively help tackle troublesome fungal diseases. The virulence and optimal growth of fungi depend on various extracellular secreted factors, among which proteases, such as serine proteases, are of particular interest. A specific extracellular proteolytic system enables fungi to survive and penetrate the tissues. Given the role of fungal proteases in infection, any molecule capable of selectively and specifically inhibiting their activity can lead to the development of potential drugs. Owing to their specific mode of action, fungal protease inhibitors can avoid fungal resistance observed with currently available treatments. Although fungal secreted proteases have been extensively studied as potential virulence factors, our understanding of the substrate specificity of such proteases remains poor. In this review, we summarize the recent advances in the design and development of specific serine protease inhibitors and provide a brief history of the compounds that inhibit fungal serine protease activity." @default.
- W4200241342 created "2021-12-31" @default.
- W4200241342 creator A5000105938 @default.
- W4200241342 creator A5066364048 @default.
- W4200241342 creator A5074114638 @default.
- W4200241342 date "2022-02-01" @default.
- W4200241342 modified "2023-10-11" @default.
- W4200241342 title "Recent advances in fungal serine protease inhibitors" @default.
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