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苯甲酰胺类化合物的合成与生物评价及其对草地贪夜蛾的杀虫活性。

Synthesis and Biological Evaluation of Benzamide Compounds as Insecticides Agents Against Spodoptera Frugiperda (Lepidoptera: Noctuidae).

机构信息

Department of Chemistry, College of Science, King Faisal University, Al-Ahsa, 31982, Saudi Arabia.

Department of Chemistry, Faculty of Science, Sohag University, Sohag, 82524, Egypt.

出版信息

Chem Biodivers. 2024 Aug;21(8):e202400948. doi: 10.1002/cbdv.202400948. Epub 2024 Aug 2.

Abstract

Due to its severe damage, Spodoptera frugiperda is receiving attention as one of the biggest dangers to world food security. Although there are numerous insecticides that are widely and successfully used to control S. frugiperda, they do not have an immediate effect. In our work focusing for synthesized twelve novel benzamide derivatives and examined their insecticidal effectiveness against S. frugiperda larvae in their second & fourth larvae instars, with the aim of further improving the insecticidal activity based on combination principles. Several spectroscopic methods, including elemental analysis, NMR & infrared spectroscopy, were employed for confirming the structure of the newly designed products. It has been discovered that most compounds show good of promising efficacy. With an LC of 24.8 mg/L for larvae in the second instar & 56.2 mg/L for larvae in the fourth instar, compound 23 was the most active. Among all compounds 11, 22 and 20 exhibited excellent results. Furthermore, a number of biological and histopathological properties of the demonstration compounds of the produced goods under laboratory conditions were also examined. This work further demonstrates the anti-proliferation of S. frugiperda and offers fresh ideas for the manufacture of benzamide derivatives.

摘要

由于其严重的破坏,草地贪夜蛾正受到关注,成为世界粮食安全的最大威胁之一。尽管有许多杀虫剂被广泛而成功地用于防治 S. frugiperda,但它们没有立即生效。在我们专注于合成的十二种新型苯甲酰胺衍生物并研究它们对 S. frugiperda 幼虫在第二和第四幼虫龄期的杀虫效果的工作中,目的是进一步根据组合原理提高杀虫活性。几种光谱方法,包括元素分析、NMR 和红外光谱,被用于确认新设计产品的结构。已经发现大多数化合物表现出良好的效果。化合物 23 的活性最高,其对第二代幼虫的 LC 为 24.8 mg/L,对第四代幼虫的 LC 为 56.2 mg/L。在所有化合物中,11、22 和 20 表现出优异的结果。此外,还在实验室条件下对所产生的化合物进行了一些生物和组织病理学特性的研究。这项工作进一步证明了 S. frugiperda 的抗增殖作用,并为苯甲酰胺衍生物的制造提供了新的思路。

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