益达胺
烟碱激动剂
乙酰胆碱受体
新烟碱
药理学
受体
烟碱乙酰胆碱受体
昆虫
乙酰胆碱
毒性
化学
兴奋剂
生物
生物化学
毒理
杀虫剂
生态学
有机化学
作者
Kazuhiko Matsuda,Steven D. Buckingham,Daniel A. Kleier,James J. Rauh,Marta Grauso,David B. Sattelle
标识
DOI:10.1016/s0165-6147(00)01820-4
摘要
Imidacloprid is increasingly used worldwide as an insecticide. It is an agonist at nicotinic acetylcholine receptors (nAChRs) and shows selective toxicity for insects over vertebrates. Recent studies using binding assays, molecular biology and electrophysiology suggest that both alpha- and non-alpha-subunits of nAChRs contribute to interactions of these receptors with imidacloprid. Electrostatic interactions of the nitroimine group and bridgehead nitrogen in imidacloprid with particular nAChR amino acid residues are likely to have key roles in determining the selective toxicity of imidacloprid. Chemical calculation of atomic charges of the insecticide molecule and a site-directed mutagenesis study support this hypothesis.
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