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Design, synthesis, insecticidal activity and 3D-QSR study for novel trifluoromethyl pyridine derivatives containing an 1,3,4-oxadiazole moiety

A series of trifluoromethyl pyridine derivatives containing 1,3,4-oxadiazole moiety was designed, synthesized and bio-assayed for their insecticidal activity. The result of bio-assays indicated the synthesized compounds exhibited good insecticidal activity against Mythimna separata and Plutella xylo...

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Detalles Bibliográficos
Autores principales: Xu, F. Z., Wang, Y. Y., Luo, D. X., Yu, G., Guo, S. X., Fu, H., Zhao, Y. H., Wu, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078298/
https://www.ncbi.nlm.nih.gov/pubmed/35540384
http://dx.doi.org/10.1039/c8ra00161h
Descripción
Sumario:A series of trifluoromethyl pyridine derivatives containing 1,3,4-oxadiazole moiety was designed, synthesized and bio-assayed for their insecticidal activity. The result of bio-assays indicated the synthesized compounds exhibited good insecticidal activity against Mythimna separata and Plutella xylostella, most of the title compounds show 100% insecticidal activity at 500 mg L(−1) and >80% activity at 250 mg L(−1) against the two pests. Compounds E18 and E27 showed LC(50) values of 38.5 and 30.8 mg L(−1) against Mythimna separata, respectively, which were close to that of avermectin (29.6 mg L(−1)); compounds E5, E6, E9, E10, E15, E25, E26, and E27 showed 100% activity at 250 mg L(−1), which were better than chlorpyrifos (87%). CoMFA and CoMSIA models with good predictability were proposed, which revealed the electron-withdrawing groups with an appropriate bulk at 2- and 4-positions of benzene ring could enhance insecticidal activity.