首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, antibacterial activity evaluation and QSAR studies of novel dispiropyrrolidines.
【24h】

Synthesis, antibacterial activity evaluation and QSAR studies of novel dispiropyrrolidines.

机译:新型双螺吡咯烷的合成,抗菌活性评估和QSAR研究。

获取原文
获取原文并翻译 | 示例
           

摘要

A series of novel dispiropyrrolidines have been synthesized through 1,3-dipolar cycloaddition of an azomethine ylide generated from sarcosine and isatin with the dipolarophile 3-benzylidene-1-methyl-pyrrolidine-2,5-dione. Their antibacterial activity was evaluated against Bacillus subtilis NCIM 2718, Staphylococcus aureus NCIM5021, Salmonella typhi NCIM2501, Pseudomonas aeruginosa NCIM 5029 and Proteus vulgaris NCIM2813 by two fold dilution method. Compound 6e exhibits reasonably good activity and compound 6c exhibits poor activity against all the organisms. The QSAR's were developed for all antibacterial activities. The models had either one or two descriptors (r2 = 0.81-0.97, , q2 = 0.57-0.92, F-ratio = 12.73-162.76). Topology, shape, charge distribution and hydrophobic nature of the molecules had pronounced effect on their antibacterial activity.
机译:通过将肌氨酸和靛红产生的偶氮甲碱内酯与偶极亲和性的3-亚苄基-1-甲基-吡咯烷-2,5-二酮进行1,3-偶极环加成反应,合成了一系列新型双螺并吡咯烷。通过两倍稀释法评估了它们对枯草芽孢杆菌NCIM 2718,金黄色葡萄球菌NCIM5021,伤寒沙门氏菌NCIM2501,铜绿假单胞菌NCIM 5029和寻常变形杆菌NCIM2813的抗菌活性。化合物6e表现出相当好的活性,而化合物6c表现出对所有生物的不良活性。 QSAR被开发用于所有抗菌活性。这些模型具有一个或两个描述符(r2 = 0.81-0.97,,q2 = 0.57-0.92,F-比= 12.73-162.76)。分子的拓扑结构,形状,电荷分布和疏水性对其抗菌活性具有显着影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号