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Design, Synthesis, and Antimicrobial Activity Evaluation of Novel Isocryptolepine Derivatives against Phytopathogenic Fungi and Bacteria

抗菌剂 细菌 微生物学 抗感染药 化学 生物 传统医学 生物技术 医学 遗传学
作者
Yan-Yan Ding,Ya‐Rui Jin,Xiong‐Fei Luo,Shaoyong Zhang,Tian‐Li Dai,Li Ma,Zhijun Zhang,Zhengrong Wu,C. Jin,Ying‐Qian Liu
出处
期刊:Journal of Agricultural and Food Chemistry [American Chemical Society]
卷期号:72 (38): 20831-20841 被引量:6
标识
DOI:10.1021/acs.jafc.4c03976
摘要

This research adopted the Fischer indole synthesis method to continue constructing a novel drug-like chemical entity based on the guidance of isocryptolepine and obtained four series of derivatives: Y, Da, Db, and Dc. The antimicrobial activity of these derivatives against plant pathogens was further evaluated. The results showed that Dc-2 had the best antifungal effect against Botrytis cinerea, and its EC50 value was up to 1.29 μg/mL. In addition, an in vivo activity test showed that the protective effect of Dc-2 on apples was 82.2% at 200 μg/mL, which was better than that of Pyrimethanil (45.4%). Meanwhile, it was found by scanning electron microscopy and transmission electron microscopy that the compound Dc-2 affected the morphology of mycelia. The compound Dc-2 was found to damage the cell membrane by PI and ROS staining. Through experiments such as leakage of cell contents, it was found that the compound Dc-2 changed the permeability of the cell membrane and caused the leakage of substances in the cell. According to the above studies, compound Dc-2 can be used as a candidate lead compound for further structural optimization and development.
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