Author:
Jiménez-Ortigosa Cristina,Paderu Padmaja,Motyl Mary R.,Perlin David S.
Abstract
ABSTRACTMK-3118 is as an orally active new antifungal in the early stage of clinical development that inhibits the biosynthesis of β-(1,3)-glucan. We evaluated thein vitroactivity of this compound against wild-type and echinocandin-resistant (ER) isolates containing mutations in theFKSgene(s) ofCandidaspp. andAspergillusspp. MK-3118 demonstrated enhanced efficacy for mostC. albicansandC. glabrataER isolates relative to caspofungin, with decreased MICs and half-maximal inhibitory concentrations (IC50s).
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
105 articles.
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