Design, Synthesis, and Insecticidal Activity of Novel Isoxazoline Compounds That Contain Meta-diamides against Fall Armyworm (Spodoptera frugiperda)

被引:16
作者
Jiang, Biaobiao [1 ]
Feng, Di [1 ]
Li, Fangyi [1 ]
Luo, Yuqin [1 ]
He, Siqi [1 ]
Dong, Yawen [2 ]
Hu, Deyu [1 ]
机构
[1] Guizhou Univ, State Key Lab Breeding Base Green Pesticide & Agr, Key Lab Green Pesticide & Agr Bioengn, Minist Educ, Guiyang 550025, Guizhou, Peoples R China
[2] Guizhou Univ, Sch Pharmaceut Sci, Guiyang 550025, Guizhou, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
fall armyworm; isoxazoline; 3D-QSAR; insecticidal activity; molecular docking; LEPIDOPTERA-NOCTUIDAE; RESISTANCE;
D O I
10.1021/acs.jafc.2c07035
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Fall armyworm (Spodoptera frugiperda) is a major migratory pest around the entire world that causes severe damage to agriculture. We designed and synthesized a series of novel isoxazoline derivatives based on the previously discovered active compound H13 to find new and effective candidates against S. frugiperda. Most of them showed excellent insecticidal activity. In addition, a three-dimensional quantitative structure???activity relationship model was established, and compound F32 was designed and synthesized based on the results. The bioassay result showed that compound F32 exhibited excellent activity against S. frugiperda (LC50 = 3.46 mg/L), which was substantially better than that of the positive control fipronil (LC50 = 78.8 mg/L). Furthermore, an insect ??-aminobutyric acid (GABA) enzyme-linked immunosorbent assay indicated that F32 can upregulate the content of GABA in insects in a manner similar to that of fipronil. Molecular docking showed that the hydrophobic effect and hydrogen-bond interactions are vital factors between the binding of F32 and receptors. All of these results suggest that compound F32 could be employed as a novel isoxazoline lead compound to control S. frugiperda.
引用
收藏
页码:1091 / 1099
页数:9
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