A small focused library of eighteen new 1,2,3-triazole tethered acetophenones has been efficiently prepared via click chemistry approach and evaluated for their antifungal and antioxidant activity.The antifungal activ...A small focused library of eighteen new 1,2,3-triazole tethered acetophenones has been efficiently prepared via click chemistry approach and evaluated for their antifungal and antioxidant activity.The antifungal activity was evaluated against five human pathogenic fungal strains：Candida albicans,Fusarium oxysporum,Aspergillus flavus,Aspergillus niger,and Cryptococcus neoformans.Among the synthesized compounds,9c,9i,and 9p found to be more potent antifungal agents that the reference standard.These 1,2,3-triazole based derivatives were also evaluated for antioxidant activity,and compound 9h was found to be the most potent antioxidant as compared to the standard drug.Furthermore,molecular docking study of the newly synthesized compounds was performed and results showed good binding mode in the active site of fungal C.albicans enzyme P450 cytochrome lanosterol14oi-demethylase.Moreover,the synthesized compounds were also analyzed for ADME properties and showed potential as good oral drug candidates.展开更多
基金the University Grant Commission-Department of Science and Technology New Delhi for financial support under UGC-SAP and DST-FIST schemes
文摘A small focused library of eighteen new 1,2,3-triazole tethered acetophenones has been efficiently prepared via click chemistry approach and evaluated for their antifungal and antioxidant activity.The antifungal activity was evaluated against five human pathogenic fungal strains：Candida albicans,Fusarium oxysporum,Aspergillus flavus,Aspergillus niger,and Cryptococcus neoformans.Among the synthesized compounds,9c,9i,and 9p found to be more potent antifungal agents that the reference standard.These 1,2,3-triazole based derivatives were also evaluated for antioxidant activity,and compound 9h was found to be the most potent antioxidant as compared to the standard drug.Furthermore,molecular docking study of the newly synthesized compounds was performed and results showed good binding mode in the active site of fungal C.albicans enzyme P450 cytochrome lanosterol14oi-demethylase.Moreover,the synthesized compounds were also analyzed for ADME properties and showed potential as good oral drug candidates.
