Silicon Incorporated Morpholine Antifungals: Design, Synthesis, and Biological Evaluation
- ACS Med Chem Lett. 2015 Sep 22;6(11):1111-6. doi: 10.1021/acsmedchemlett.5b00245.
- 1. Division of Organic Chemistry and Biochemical Sciences Division, CSIR-National Chemical Laboratory , Dr. Homi Bhabha Road, Pune-411008, India.
- 2. National Research Centre for Grapes , Manjri, Solapur Road, Pune-412307, India.
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.