| Literature DB >> 28820587 |
Yasumichi Onozaki1, Ryo Horikoshi1, Ikuya Ohno1, Shigeki Kitsuda1, Kathleen A Durkin2, Tomonori Suzuki3, Chiaki Asahara3, Natsuko Hiroki3, Rena Komabashiri3, Rikako Shimizu3, Shogo Furutani4, Makoto Ihara4, Kazuhiko Matsuda4, Masaaki Mitomi1, Shinzo Kagabu5, Katsuhito Uomoto1, Motohiro Tomizawa3.
Abstract
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.Entities:
Keywords: flupyrimin; nicotinic acetylcholine receptor; nicotinic insecticide; pyridinylidene and trifluoroacetyl pharmacophores
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Year: 2017 PMID: 28820587 DOI: 10.1021/acs.jafc.7b02924
Source DB: PubMed Journal: J Agric Food Chem ISSN: 0021-8561 Impact factor: 5.279