1.Synthesis and antifungal evaluation of chalcone derivatives combined with fluconazole against drug-resistant Candida albicans
Yunhong SHEN ; Hongjie CHEN ; Zewei MAO ; Zhengxiao HUANG ; Chunyan HU
Journal of China Pharmaceutical University 2023;54(5):564-568
Chalcone is a common scaffold in natural products with optimal properties and biological activities.In this study, we designed and prepared eight new coumarin-chalcone derivatives (5a-5h), and confirmed their structures by 1H NMR and 13C NMR. Their in vitro antifungal activity combined with fluconazole (FLC) against drug-resistant Candida albicans was tested by microdilution method.The results indicated that most chalcone derivatives showed good antifungal activity against drug resistant Candida albicans with FLC, particularly with compound 5g displaying better antifungal activity (MIC50 = 5.60 μg/mL) than FLC (MIC50 = 200 μg/mL) when combined with FLC, so, these derivatives could be used as synergists of antifungal drugs.
2.Synthesis and anti-tumor activity in vitro of N-hetercycle substituted benzofuran derivatives
Zewei MAO ; Chunping WAN ; Yuan JIANG ; Wenlian GUO ; Gaoxiong RAO
Journal of China Pharmaceutical University 2015;46(1):58-61
To discover the novel compounds with biological activity, N-hetercycle substituted derivatives were synthesized based on the structure of benzofuran. A series of novel N-hetercycle substituted benzofuran derivatives(2a-2j)were synthesized by the reaction of 2-(4′-florobenzoyl)benzofuran with N-heterocyclic compounds. And the structures were characterized by 1H NMR, 13C NMR and HRMS. Their anti-tumor activities were studied in vitro against a panel of human tumor cell lines(HeLa, A549 and H1975)by the MTT assay. The results indicate that compounds 2a, 2f and 2j are the most potent within this series of compounds against human tumor cell lines, showing that they are promising lead compounds for further structural modifications and biological evaluation.