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设计并合成了一些新型结构多样的噻蒽酮衍生物,作为防治植物病原菌真菌的杀菌剂。

Design and synthesis of some novel structurally diverse thiochroman derivatives as fungicides against phytopathogenic fungi.

机构信息

College of Pharmacy, Guizhou Provincial Engineering Technology Research Center for Chemical Drug R&D, Guizhou Medical University, Guiyang, P. R. China.

出版信息

Pest Manag Sci. 2024 Dec;80(12):6607-6619. doi: 10.1002/ps.8400. Epub 2024 Sep 5.

Abstract

BACKGROUND

Plant diseases infected by pathogenic fungi have a devastating effect on global agricultural and food industry yields. The development of novel, environmentally friendly, and efficient fungicides is an important technique for preventing and combatting phytopathogenic fungi.

RESULTS

Herein, 99 thiochroman-based derivatives containing hydroxyl, sulfoxide, sulfone, carbonyl, double bond, amino, imine, oxime, oxime ester, and amide moieties were synthesized. The antifungal activities of the target compounds against ten typical phytopathogenic fungi were also investigated. The bioassay results illustrated that most of the target compounds exhibited moderate to excellent antifungal effects against the tested fungi in vitro. Among these, thiochroman-oxime derivatives (12a-12m) exerted a promising inhibition effect, especially against Fusarium solani, Fusarium graminearum, Valsa mali, and Botrytis cinerea strains. Furthermore, the compounds 12f and 12g markedly suppressed the spore germination germ and tube growth. At the same time, they exerted excellent protective effects against potatoes infected by F. solani, making them superior to commercial fungicides Hymexazol and Chlorothalonil. Notably, the compounds 12d and 12f also showed excellent protective effects against cherry tomatoes infected by B. cinerea. Further mechanistic studies revealed that compound 12f exerted an antifungal effect by overtly altering the mycelium structure and remarkably increasing cell membrane permeability. Fortunately, the excellent bioactive compounds showed good safety against human hepatic cell lines (WRL-68). The preliminary structure-activity relationship analysis revealed that the introduction of hydroxyl or oxime fragments at the thiopyran ring might be significantly beneficial to antifungal activity.

CONCLUSION

This study provides thiochroman compounds that can be used in the development of novel botanical fungicides for the management of phytopathogenic fungi. © 2024 Society of Chemical Industry.

摘要

背景

被病原真菌感染的植物病害对全球农业和食品产业的产量造成了毁灭性的影响。开发新型、环保且高效的杀菌剂是预防和防治植物病原真菌的重要技术。

结果

在此,合成了 99 种含有羟基、亚砜、砜、羰基、双键、氨基、亚胺、肟、肟酯和酰胺部分的噻蒽酮类衍生物。还研究了目标化合物对十种典型植物病原真菌的抗真菌活性。生物测定结果表明,大多数目标化合物对测试真菌在体外均表现出中等至优异的抗真菌作用。在这些化合物中,噻蒽酮肟衍生物(12a-12m)表现出对尖孢镰刀菌、禾谷镰刀菌、苹果腐烂病菌和葡萄孢菌的抑制作用尤为显著。此外,化合物 12f 和 12g 显著抑制孢子萌发和管生长。同时,它们对受尖孢镰刀菌感染的马铃薯表现出优异的保护作用,优于商业杀菌剂 hymexazol 和百菌清。值得注意的是,化合物 12d 和 12f 对受灰葡萄孢菌感染的樱桃番茄也表现出优异的保护作用。进一步的机制研究表明,化合物 12f 通过明显改变菌丝体结构和显著增加细胞膜通透性来发挥抗真菌作用。幸运的是,优秀的生物活性化合物对人肝细胞系(WRL-68)表现出良好的安全性。初步的构效关系分析表明,噻吩环上引入羟基或肟片段可能对抗真菌活性有显著的益处。

结论

本研究提供了噻蒽酮类化合物,可用于开发新型植物源杀菌剂来防治植物病原真菌。© 2024 化学工业协会。

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