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新型含芳氧吡啶基乙胺模块的吡唑甲酰胺的合成及生物活性。

Synthesis and Biological Activities of Novel Pyrazole Carboxamides Containing an Aryloxypyridyl Ethylamine Module.

机构信息

College of Science, China Agricultural University, Beijing 100193, China.

Institute of Agro-Food Science and Technology, Shandong Academy of Agricultural Sciences, Jinan 250100, Shandong Province, China.

出版信息

J Agric Food Chem. 2024 Feb 21;72(7):3342-3353. doi: 10.1021/acs.jafc.3c06753. Epub 2024 Feb 9.

Abstract

Pyrazole carboxamide is widely utilized in agricultural crop protection. In this research, we synthesized two classes of compounds, namely, pyrazole-5-carboxamide () and pyrazole-4-carboxamide (), which are distinguished by the inclusion of the -1-(6-aryloxypyridin-3-yl) ethylamine skeleton. This design was inspired by the frequent occurrence of diaryl ether modules in pesticide molecules. The bioassay results revealed that some compounds exhibit higher insecticidal activity (IA) than , while some compounds display stronger fungicidal activity compared to . This suggests that pyrazolyl plays a crucial role in determining the selectivity of these compounds toward different biological species. Notably, compound not only retains the potent activity of tolfenpyrad, the exact lead compound of , against Lepidoptera pest and Thysanoptera pest but also shows excellent IA against pests with piercing-sucking mouthparts, such as Koch and . This research has important implications for the control of pests with piercing-sucking mouthparts and the development of new insecticides and fungicides. The findings highlight the potential of inhibitory complex I as an effective control target for these pests, particularly those that have developed resistance to traditional insecticides. Additionally, it sheds light on the binding mode of and complex II, which serves as a negative reference for the design of SDHI fungicides. The study emphasizes the significance of pyrazolyl in determining selectivity in biological species and identifies avenues for future research in enhancing the biological activity of amino modules. The discovery of ()- not only presents a promising candidate compound for pesticide development but also provides valuable insights into the inhibitory effect of a respiratory chain complex on piercing-sucking insect pests. These findings have important implications in both theory and practice, offering new directions for pest control strategies and pesticide and fungicide development.

摘要

吡唑甲酰胺在农业作物保护中被广泛应用。在本研究中,我们合成了两类化合物,即吡唑-5-甲酰胺()和吡唑-4-甲酰胺(),它们的区别在于包含了-1-(6-芳基氧吡啶-3-基)乙胺骨架。这一设计灵感来源于农药分子中经常出现的二芳基醚模块。生物测定结果表明,一些化合物()表现出比化合物()更高的杀虫活性(IA),而一些化合物()则表现出比化合物()更强的杀菌活性。这表明吡唑基在确定这些化合物对不同生物物种的选择性方面起着关键作用。值得注意的是,化合物()不仅保留了先导化合物()对鳞翅目害虫和缨翅目害虫的高效活性,而且对具有刺吸式口器的害虫如桃蚜和烟粉虱也表现出优异的杀虫活性。本研究对防治具有刺吸式口器的害虫以及开发新的杀虫剂和杀菌剂具有重要意义。研究结果表明,抑制复合体 I 作为这些害虫的有效控制靶标具有潜力,特别是对传统杀虫剂产生抗性的害虫。此外,它还揭示了与复合体 II 的结合模式,为 SDHI 杀菌剂的设计提供了一个负面参考。该研究强调了吡唑基在确定生物物种选择性方面的重要性,并确定了增强氨基酸模块生物活性的未来研究方向。()-的发现不仅为农药开发提供了一个有前途的候选化合物,还为呼吸链复合物对刺吸式昆虫害虫的抑制作用提供了有价值的见解。这些发现无论是在理论还是实践方面都具有重要意义,为害虫防治策略和杀虫剂及杀菌剂的开发提供了新的方向。

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