Synthesis of novel derivatives of camptothecin as potential insecticides

被引:34
作者
Liu, Ying-Qian [1 ,2 ]
Yang, Liu [3 ]
Zhao, Yong-Long [2 ]
Li, Hong-Yu [1 ,2 ]
机构
[1] Lanzhou Univ, Sch Life Sci, MOE Key Lab Arid & Grassland Ecol, Lanzhou 730000, Peoples R China
[2] Lanzhou Univ, Sch Pharm, Lanzhou 730000, Peoples R China
[3] Lanzhou Jiaotong Univ, Environm & Municipal Engn Sch, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
Camptothecin; Nitroxides; Antifeedant activity; Insecticidal activity; Mythimna separate; NITROXYL RADICALS; PODOPHYLLOTOXIN; DEOXYPODOPHYLLOTOXIN; PERSPECTIVES; ACUMINATA; AGENTS; LARVAE;
D O I
10.1016/j.pestbp.2010.06.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In an attempt to find the biorational pesticides, a series of novel camptothecin derivatives were synthesized via a simple modification of the carbodiimide method using the combination of scandium triflate (Sc(OTf)(3)) and 4-dimethylaminopyridine (DMAP), and their structures were identified by IR, ESR, HRMS and (1)H NMR. Their antifeedant effect and insecticidal activity against third-instar larva of Mythimna separate were examined. The results of preliminary bioassays showed that these compounds exhibited less potent antifeedant activity than camptothecin. Also, all of these derivatives of camptothecin showed delayed insecticidal activity, which differs from traditional neurotoxic insecticides. The results suggested that 20-hydroxyl group in the camptothecin derivatives is essential to keep the insecticidal activity and nature of the substitutes has a major impact on insecticidal activity of these compounds. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:219 / 223
页数:5
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