位置:成果数据库 > 期刊 > 期刊详情页
新型邻甲酰胺基间苯二甲酰胺类化合物的设计合成及生物活性
  • 期刊名称:高等学校化学学报
  • 时间:0
  • 页码:1750-1754
  • 语言:中文
  • 分类:TQ457.202[化学工程—农药化工] TQ414
  • 作者机构:[1]State Key Laboratory of Elemento-Organic Chemistry, Institute of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China
  • 相关基金:Supporting information for this article is available on the WWW under http://dx.doi.org/10.1002/cjoc.2011 00745 or from the author. Acknowledgement This work was supported by the National Natural Science Foundation of China (No. 20872069), National Basic Research Program of China (No. 2010CB126106), the National Key Technologies R&D Program (No. 2011BAE06B05) and Tianjin Natural Science Foundation (No. 11JCYBJC08600)
  • 相关项目:基于鱼尼丁受体新靶标的绿色杀虫剂的设计合成、生物活性及构效关系研究
中文摘要:

以便在 ryanodine 受体(RyR ) 上与新行动模式发现新奇杀虫药剂,一系列新奇酞酸酸 diamide 衍生物被设计并且综合。所有混合物被 1H NMR 系列和 HRMS 描绘。生物活动评价的初步的结果显示一些标题混合物对 Mythimna separata, Spodoptera exigua,和 Plutella xylostella 展出了优秀杀虫的活动。标题混合物 3-nitro-N-cyclopropyl-N-[2-methyl-4-(perfluoropropan-2-yl ) 苯基] phthalamide (4a ) 比控制(chlorantraniliprole ) 对有菱形斑纹的蛾是更有效的。从 Spodoptera exigua 的神经原的细胞内部的钙上的一些标题混合物的效果证明标题混合物是 RyR 使活跃之物。

英文摘要:

In order to discover novel insecticides with the new action mode on ryanodine receptor (RyR), a series of novel phthalic acid diamide derivatives were designed and synthesized. All compounds were characterized by 1H NMR spectra and HRMS. The preliminary results of biological activity assessment indicated that some title compounds exhibited excellent insecticidal activities against Mythimna separata, Spodoptera exigua, and Plutella xylostella. The title compound 3-nitro-N-cyclopropyl-N'-[2-methyl-4-(perfluoropropan-2-yl)phenyl]phthalamidte (4a) was more efficient against diamondback moths than the control (chlorantraniliprole). The effects of some title compounds on intracellular calcium of neurons from the Spodoptera exigua proved that the title compounds were RyR activators.

同期刊论文项目
同项目期刊论文