喹啉
菌核病
杀菌剂
EC50型
化学
抗真菌
体内
奎宁
膜透性
天然产物
体外
生物化学
立体化学
生物
有机化学
膜
植物
微生物学
生物技术
免疫学
疟疾
作者
Guan‐Zhou Yang,Jia-Kai Zhu,Xiaodan Yin,Yin-Fang Yan,Yuling Wang,Xiaofei Shang,Ying‐Qian Liu,Zhong-Min Zhao,Jingwen Peng,Hua Liu
标识
DOI:10.1021/acs.jafc.9b04224
摘要
Inspired by quinine and its analogues, we designed, synthesized, and evaluated two series of quinoline small molecular compounds (a and 2a) and six series of quinoline derivatives (3a-f) for their antifungal activities. The results showed that compounds 3e and 3f series exhibited significant fungicidal activities. Significantly, compounds 3f-4 (EC50 = 0.41 μg/mL) and 3f-28 (EC50 = 0.55 μg/mL) displayed the superior in vitro fungicidal activity and the potent in vivo curative effect against Sclerotinia sclerotiorum. Preliminary mechanism studies showed that compounds 3f-4 and 3f-28 could cause changes in the cell membrane permeability, accumulation of reactive oxygen species, loss of mitochondrial membrane potential, and effective inhibition of germination and formation of S. sclerotiorum sclerotia. These results indicate that compounds 3f-4 and 3f-28 are novel potential fungicidal candidates against S. sclerotiorum derived from natural products.
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