Design, Synthesis, and Fungicidal Activities of Novel 5-Methyl-1H-1,2,3-trizole-4-carboxyl Amide Analogues

被引:3
|
作者
Wang, Zhen-Jun [1 ]
Yang, Hui-Hui [1 ]
Tian, Lei [1 ]
Zhao, Wei-Guang [1 ,2 ]
机构
[1] Nankai Univ, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China
[2] Nankai Univ, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
Succinate dehydrogenase inhibitors; 1,2,3-Triazole; fungicide; fungicidal activity relationship; synthesis; BIOLOGICAL-ACTIVITIES; SUCCINATE; RESISTANCE;
D O I
10.2174/1573406412666151112125006
中图分类号
R914 [药物化学];
学科分类号
100701 ;
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 N-benzyl-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 mu g/mL) was lower than that of chlorothalonil (12.3 mu g/mL).
引用
收藏
页码:290 / 295
页数:6
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