查尔酮
抗真菌
吡唑
化学
立体化学
作用机理
肺孢子虫病
组合化学
生物化学
生物
植物
体外
微生物学
作者
Yufang Zhang,Xingping Luo,Qing Zhou,Xue Geng,Lang Xing,Qingxue Hu,Han Yang,Xiaoyan Pan,Wei Xue
标识
DOI:10.1021/acs.jafc.5c06092
摘要
16 chalcone derivatives containing pyrazole were synthesized. The antifungal activity of the target compounds against 8 pathogenic fungi was measured. The results of the in vitro antifungal activity test indicated that the EC50 of Z10 for Phomopsis sp. (P.s.) was 12.5 μg/mL, which was better than those of the control prescription drugs azoxystrobin (Az, 24.9 μg/mL) and flupidazamide (Fl, 282.6 μg/mL). The molecular docking, density functional theory (DFT) calculation, and molecular electrostatic potential results showed that the binding affinity of Z10 to the SDH protein was better than that of Fl. The results of scanning electron microscopy (SEM) and fluorescence microscopy (FM) showed that Z10 disrupted the fullness of the pathogenic fungal membrane, causing the cell membrane to curve, fork, and fold and affecting the normal growth of mycelium. Further studies found that the change of membrane integrity of pathogenic fungi led to the leakage of cytoplasmic contents and the increase of malondialdehyde (MDA) content.
科研通智能强力驱动
Strongly Powered by AbleSci AI