Suppr超能文献

新型丙烯海松酸三唑衍生物作为有前景的抗真菌剂的发现。

Discovery of novel acrylopimaric acid triazole derivatives as promising antifungal agents.

作者信息

Han Xu, Xu Renle, Gu Shihao, Kong Yue, Lou Yuhang, Gao Yanqing, Shang Shibin, Song Zhanqian, Song Jie, Li Jian

机构信息

Jiangsu Province Key Laboratory of Biomass Energy and Materials, College of Forestry, Northwest A&F University, Yangling, P. R. China.

College of Plant Protection, Northwest A&F University, Yangling, P. R. China.

出版信息

Pest Manag Sci. 2024 Aug;80(8):3988-3996. doi: 10.1002/ps.8102. Epub 2024 Apr 16.

Abstract

BACKGROUND

To further develop potential natural fungicides, two series of new acrylopimaric acid triazole derivatives were synthesized, and their antifungal activities were tested and evaluated.

RESULTS

In vitro antifungal activity results indicated that compound 5m exhibited significant inhibitory activity against Rhizoctonia solani with an half maximal effective concentration (EC) value of 1.528 mg/L. Its antifungal effect was comparable to that of the commercially available fungicide fluconazole, epoxiconazole and propiconazole (EC values of 1.441, 0.815 and 1.173 mg/L). Subsequently, in vivo studies were conducted on compound 5m, which revealed its significant protective and curative effects against R. solani. In addition, physiological and biochemical studies showed that compound 5m could disrupt the morphology and ultrastructure of R. solani mycelium, increase cell membrane permeability, inhibit ergosterol synthesis, and enhance the activity of defense enzymes in rice plants. Three-dimensional quantitative structure-activity relationship (3D-QSAR) studies revealed that the molecular structure significantly influenced the binding of compound 5m to the receptor, thereby enhancing its antifungal activity.

CONCLUSION

Compound 5m exhibits excellent antifungal activity against R. solani, making it a promising candidate fungicide for the prevention and control of R. solani. © 2024 Society of Chemical Industry.

摘要

背景

为进一步开发潜在的天然杀菌剂,合成了两个系列的新型丙烯酸海松酸三唑衍生物,并对其抗真菌活性进行了测试和评估。

结果

体外抗真菌活性结果表明,化合物5m对立枯丝核菌表现出显著的抑制活性,半数有效浓度(EC)值为1.528mg/L。其抗真菌效果与市售杀菌剂氟康唑、环氧唑和丙环唑相当(EC值分别为1.441、0.815和1.173mg/L)。随后,对化合物5m进行了体内研究,结果显示其对立枯丝核菌具有显著的保护和治疗作用。此外,生理生化研究表明,化合物5m可破坏立枯丝核菌菌丝体的形态和超微结构,增加细胞膜通透性,抑制麦角甾醇合成,并增强水稻植株中防御酶的活性。三维定量构效关系(3D-QSAR)研究表明,分子结构显著影响化合物5m与受体的结合,从而增强其抗真菌活性。

结论

化合物5m对立枯丝核菌表现出优异的抗真菌活性,使其成为防治立枯丝核菌的有前景的候选杀菌剂。©2024化学工业协会。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验