烟碱乙酰胆碱受体
烟碱激动剂
化学
益达胺
药效团
乙酰胆碱受体
受体
效力
药理学
生物化学
立体化学
生物
体外
农学
杀虫剂
作者
Yasumichi Onozaki,Ryo Horikoshi,Ikuya Ohno,Shigeki Kitsuda,Kathleen A. Durkin,Tomonori Suzuki,Chiaki Asahara,Natsuko Hiroki,Rena Komabashiri,Rikako Shimizu,Shogo Furutani,Makoto Ihara,Kazuhiko Matsuda,Masaaki Mitomi,Shinzo Kagabu,Uomoto Katsuhito,Motohiro Tomizawa
标识
DOI:10.1021/acs.jafc.7b02924
摘要
A novel chemotype insecticide flupyrimin (FLP) [N-[(E)-1-(6-chloro-3-pyridinylmethyl)pyridin-2(1H)-ylidene]-2,2,2-trifluoroacetamide], discovered by Meiji Seika Pharma, has unique biological properties, including outstanding potency to imidacloprid (IMI)-resistant rice pests together with superior safety toward pollinators. Intriguingly, FLP acts as a nicotinic antagonist in American cockroach neurons, and [3H]FLP binds to the multiple high-affinity binding components in house fly nicotinic acetylcholine (ACh) receptor (nAChR) preparation. One of the [3H]FLP receptors is identical to the IMI receptor, and the alternative is IMI-insensitive subtype. Furthermore, FLP is favorably safe to rats as predicted by the very low affinity to the rat α4β2 nAChR. Structure-activity relationships of FLP analogues in terms of receptor potency, featuring the pyridinylidene and trifluoroacetyl pharmacophores, were examined, thereby establishing the FLP molecular recognition at the Aplysia californica ACh-binding protein, a suitable structural surrogate of the insect nAChR. These FLP pharmacophores account for the excellent receptor affinity, accordingly revealing differences in its binding mechanism from IMI.
科研通智能强力驱动
Strongly Powered by AbleSci AI