首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, structure and structure-activity relationship analysis of caffeic acid amides as potential antimicrobials.
【24h】

Synthesis, structure and structure-activity relationship analysis of caffeic acid amides as potential antimicrobials.

机译:咖啡酸酰胺作为潜在抗菌剂的合成,结构及构效关系分析。

获取原文
获取原文并翻译 | 示例
           

摘要

A series of caffeic acid amides 1-23 were synthesized and nine of which (13-17, 19-21 and 23) were reported for the first time. The chemical structures of these compounds were confirmed by means of 1H NMR, ESI MS and elemental analyses. Compound 15 was determined by single-crystal X-ray diffraction analysis. All of the compounds were assayed for antibacterial (Bacillus subtilis, Escherichia coli, Pseudomonas fluorescens and Staphylococcus aureus) and antifungal (Aspergillus niger, Candida albicans and Trichophyton rubrum) activities by MTT method. Compounds 10-12, 15, 18 and 21 showed considerable antibacterial activities against B. subtilis with MICs of 7.95, 6.25, 3.89, 1.18, 3.12 and 15.5 microg/mL, respectively. Structure-activity relationship analysis disclosed that caffeic acid anilides with electron-donating groups at p-position of benzene ring have better inhibitory activities.
机译:合成了一系列咖啡酸酰胺1-23,首次报道了其中的9种(13-17、19-21和23)。这些化合物的化学结构通过1 H NMR,ESI MS和元素分析得到证实。通过单晶X射线衍射分析确定化合物15。通过MTT法测定所有化合物的抗菌活性(枯草芽孢杆菌,大肠杆菌,荧光假单胞菌和金黄色葡萄球菌)和抗真菌活性(黑曲霉,白色念珠菌和红毛癣菌)。化合物10-12、15、18和21对枯草芽孢杆菌显示出显着的抗菌活性,MIC分别为7.95、6.25、3.89、1.18、3.12和15.5 microg / mL。结构-活性关系分析表明,在苯环对位具有供电子基团的咖啡酸酐具有更好的抑制活性。

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