摘要
新型异唑啉类杀虫剂fluralaner通过干扰γ-氨基丁酸(GABA)门控氯离子通道发挥作用。作为新型高效GABA门控氯离子通道干扰剂,与环戊二烯类、苯基吡唑类和大环内酯类杀虫剂相比,fluralaner在分子结构、作用位点、选择性以及交互抗性等方面均有显著差异。本文综述了fluralaner及其衍生物的研发、毒性、防治范围以及作用机理等,并预测了其应用前景。
Fluralaner acts as a novel type of isoxazoline insecticides by interfere with ~/-aminobutyric acid(GABA) gated chloride channel. It displays remarkable differences in molecular structure, site of action, selectivity and cross-resistance comparing to cyclodience, phenylpyrazole and macrolides insecticides which have similar mode of action in interfering with GABA gated chloride channel. The invention, toxicity, insecticidal spectrum and mechanism of fluralaner were summarized. The prospect of fluralaner and isoxazoline insecticides were also included.
出处
《农药学学报》
CAS
CSCD
北大核心
2015年第3期251-256,共6页
Chinese Journal of Pesticide Science
基金
国家公益性行业(农业)科研专项(201303017)