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Silicon Incorporated Morpholine Antifungals: Design, Synthesis, and Biological Evaluation
Gorakhnath R Jachak1, Remya Ramesh1, Duhita G Sant1
1Division of Organic Chemistry and Biochemical Sciences Division, CSIR-National Chemical Laboratory , Dr. Homi Bhabha Road, Pune-411008, India.
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.
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