酰胺
杀菌剂
组合化学
化学
立体化学
有机化学
生物
植物
作者
Zhenjun Wang,Hui-Hui Yang,Lei Tian,Wei‐Guang Zhao
出处
期刊:Medicinal Chemistry
[Bentham Science Publishers]
日期:2016-03-31
卷期号:12 (3): 290-295
被引量:3
标识
DOI:10.2174/1573406412666151112125006
摘要
Succinate dehydrogenase inhibitors (SDHIs) are fungicides with an amide bond widely used to control plant diseases caused by phytopathogenic fungi. Because of broad spectrum activity of new SDHIs, they have attracted wide attention from the research community. A series of structurally novel SDHIs with a bioactive 1,2,3-triazole moiety were designed and synthesized. Bioactivity screening showed that some of designed N-phenethyl-1,2,3-trizole-4-carboxyl amide analogues exhibited good fungicidal activities toward Sclerotinia sclerotiorum and Botrytis cinerea, while some of Nbenzyl- 1,2,3-trizole-4-carboxyl amide analogues exhibited good fungicidal activities toward Phytophthora capsici and Cercospora arachidicola. EC50 value of compound 5d against Cercospora arachidicola (6.6 µg/mL) was lower than that of chlorothalonil (12.3 µg/mL). Keywords: Succinate dehydrogenase inhibitors, 1, 2, 3-Triazole, fungicide, fungicidal activity relationship, synthesis.
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