| Literature DB >> 26617963 |
Gorakhnath R Jachak1, Remya Ramesh1, Duhita G Sant1, Shweta U Jorwekar1, Manjusha R Jadhav2, Santosh G Tupe1, Mukund V Deshpande1, D Srinivasa Reddy1.
Abstract
Known morpholine class antifungals (fenpropimorph, fenpropidin, and amorolfine) were synthetically modified through silicon incorporation to have 15 sila-analogues. Twelve sila-analogues exhibited potent antifungal activity against different human fungal pathogens such as Candida albicans, Candida glabrata, Candida tropicalis, Cryptococcus neoformans, and Aspergillus niger. Sila-analogue 24 (fenpropimorph analogue) was the best in our hands, which showed superior fungicidal potential than fenpropidin, fenpropimorph, and amorolfine. The mode of action of sila-analogues was similar to morpholines, i.e., inhibition of sterol reductase and sterol isomerase enzymes of ergosterol synthesis pathway.Entities:
Keywords: Antifungal drugs; Candida albicans; ergosterol biosynthesis; morpholines; sila-analogues
Year: 2015 PMID: 26617963 PMCID: PMC4645241 DOI: 10.1021/acsmedchemlett.5b00245
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345