首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >NOVEL NITENPYRAM ANALOGUES WITH TETRAHYDROPYRIDONE-FIXED CZS-CONFIGURATION: SYNTHESIS, INSECTICIDAL ACTIVITIES, AND MOLECULAR DOCKING STUDIES
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NOVEL NITENPYRAM ANALOGUES WITH TETRAHYDROPYRIDONE-FIXED CZS-CONFIGURATION: SYNTHESIS, INSECTICIDAL ACTIVITIES, AND MOLECULAR DOCKING STUDIES

机译:具有四氢吡啶酮固定的CZS构型的新型内酯类似物:合成,杀虫活性和分子对接研究

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摘要

To make further researches on the diversity of nitenpyram analogues with a cis-nitromethylene configuration, a series of cis-nitenpyram analogues (3a-q) with tetrahydropyridone-fixed cis-configuration were designed and synthesized. Preliminary bioassays showed that most of the designed nitenpyram analogues exhibited good insecticidal activity at 100 mg/L against Nilaparvata lugens and Myzus persicae, while analogues 3n afforded the best in vitro activity. Modeling the ligand-receptor complexes by molecular docking study revealed the analogues 3 with various substituents on phenyl show their different binding affinities to the insect nAChR, which also explained the structure-activity relationships observed in vitro.
机译:为了进一步研究具有顺式-硝基亚甲基构型的硝苯并吡喃类似物的多样性,设计并合成了具有四氢吡啶酮固定的顺式构型的一系列顺式-nitenpyram类似物(3a-q)。初步的生物分析表明,大多数设计的硝苯吡喃类似物在100 mg / L时对褐飞虱和桃蚜有良好的杀虫活性,而类似物3n在体外具有最佳的杀虫活性。通过分子对接研究对配体-受体复合物进行建模,发现在苯基上具有各种取代基的类似物3与昆虫nAChR具有不同的结合亲和力,这也解释了体外观察到的结构-活性关系。

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