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新型植物源杀虫剂先导化合物的探索:β-二氢沉香呋喃衍生物的合成及杀虫活性

Exploration of Novel Botanical Insecticide Leads: Synthesis and Insecticidal Activity of β-Dihydroagarofuran Derivatives.

作者信息

Zhao Ximei, Xi Xin, Hu Zhan, Wu Wenjun, Zhang Jiwen

机构信息

College of Science, Northwest A&F University , Yangling, Shaanxi 712100, People's Republic of China.

Key Laboratory of Botanical Pesticide R&D in Shaanxi Province , Yangling, Shaanxi 712100, People's Republic of China.

出版信息

J Agric Food Chem. 2016 Feb 24;64(7):1503-8. doi: 10.1021/acs.jafc.5b05782. Epub 2016 Feb 15.

Abstract

The discovery of novel leads and new mechanisms of action is of vital significance to the development of pesticides. To explore lead compounds for botanical insecticides, 77 β-dihydroagarofuran derivatives were designed and synthesized. Their structures were mainly confirmed by (1)H NMR, (13)C NMR, DEPT-135°, IR, MS, and HRMS. Their insecticidal activity was evaluated against the third-instar larvae of Mythimna separata Walker, and the results indicated that, of these derivatives, eight exhibited more promising insecticidal activity than the positive control, celangulin-V. Particularly, compounds 5.7, 6.6, and 6.7 showed LD50 values of 37.9, 85.1, and 21.1 μg/g, respectively, which were much lower than that of celangulin-V (327.6 μg/g). These results illustrated that β-dihydroagarofuran ketal derivatives can be promising lead compounds for developing novel mechanism-based and highly effective botanical insecticides. Moreover, some newly discovered structure-activity relationships are discussed, which may provide some important guidance for insecticide development.

摘要

新型先导化合物和新作用机制的发现对农药的发展至关重要。为了探索植物源杀虫剂的先导化合物,设计并合成了77种β-二氢沉香呋喃衍生物。其结构主要通过¹H NMR、¹³C NMR、DEPT - 135°、IR、MS和HRMS进行确证。对其杀虫活性进行了针对粘虫(Mythimna separata Walker)三龄幼虫的评价,结果表明,在这些衍生物中,有8种表现出比阳性对照苦皮藤素V更具前景的杀虫活性。特别地,化合物5.7、6.6和6.7的LD50值分别为37.9、85.1和21.1 μg/g,远低于苦皮藤素V的LD50值(327.6 μg/g)。这些结果表明,β-二氢沉香呋喃缩酮衍生物有望成为开发基于新作用机制的高效植物源杀虫剂的先导化合物。此外,还讨论了一些新发现的构效关系,这可能为杀虫剂的开发提供一些重要指导。

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