Design, Synthesis, and Insecticidal Activity of Novel Isoxazoline Diacylhydrazine Compounds as GABA Receptor Inhibitors

被引:9
作者
Li, Yahui [1 ,2 ]
Zhang, Wenbo [1 ]
Wu, Zengxue [1 ]
Song, Baoan [1 ]
Song, Runjiang [1 ]
机构
[1] Guizhou Univ, Minist Educ, Key Lab Green Pesticide & Agr Bioengn, Natl Key Lab Green Pesticide y, Natl Key Lab Green Pesticide, Guiyang 550025, Peoples R China
[2] Anhui Agr Univ, Sch Resources & Environm, Key Lab Agrifood Safety Anhui Prov, Hefei 230036, Peoples R China
基金
中国国家自然科学基金;
关键词
isoxazoline compounds; diacylhydrazine moiety; insecticidal activities; proteomics; molecular docking; mechanism; FIELD-EVOLVED RESISTANCE; PLUTELLA-XYLOSTELLA; DIAMONDBACK MOTH; CHLORANTRANILIPROLE; MANAGEMENT; DISCOVERY; ECOLOGY;
D O I
10.1021/acs.jafc.2c08880
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
A series of isoxazoline derivatives containing diacylhydrazine moieties were designed and synthesized as potential insecticides. Most of these derivatives exhibited good insecticidal activities against Plutella xylostella, and some compounds exhibited excellent insecticidal activities against Spodoptera frugiperda. Especially, D14 showed outstanding insecticidal activity against P. xylostella (LC50 = 0.37 mu g/mL), which was superior to that of ethiprole (LC50 = 2.84 mu g/mL) and tebufenozide (LC50 = 15.3 mu g/ mL) and similar to that of fluxametamide (LC50 = 0.30 mu g/mL). Remarkably, the insecticidal activity of D14 against S. frugiperda (LC50 = 1.72 mu g/mL) was superior to that of chlorantraniliprole (LC50 = 3.64 mu g/mL) and tebufenozide (LC50 = 60.5 mu g/mL) but lower than that of fluxametamide (LC50 = 0.14 mu g/mL). The results of electrophysiological experiments, molecular docking, and proteomics experiments indicate that compound D14 acts by interfering with the y-aminobutyric acid receptor to control pests.
引用
收藏
页码:6561 / 6569
页数:9
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