...
首页> 外文期刊>Russian Journal of General Chemistry >Synthesis and antimicrobial activity of novel substituted 4-[3-(1H-benzimidazol-2-yl)-4-hydroxybenzyl]-2-(1H-benzimidazol-2-yl)phenol derivatives
【24h】

Synthesis and antimicrobial activity of novel substituted 4-[3-(1H-benzimidazol-2-yl)-4-hydroxybenzyl]-2-(1H-benzimidazol-2-yl)phenol derivatives

机译:新型取代的4- [3-(1H-苯并咪唑-2-基)-4-羟基苄基] -2-(1H-苯并咪唑-2-基)酚衍生物的合成和抗微生物活性

获取原文
获取原文并翻译 | 示例
           

摘要

A series of novel substituted bis-benzimidazole derivatives were synthesized by reaction of 5,5'-methylenebis(2-hydroxybenzaldehyde) with various substituted o-phenylenediamines in glacial acetic acid. The structure of the newly synthesized compounds was elucidated by H-1 and C-13 NMR, FT-IR, and MS spectra, and their antimicrobial activity against gram positive and gram negative bacteria and antifungal activity were evaluated. The thienyl-substituted derivative showed significant activity against Bacillus licheniformis. Bacillus subtilis, Staphylococcus aureus, Klebsiella pneumonia (bacteria), and Fusarium solani (fungi). The activities of the fluoro-substituted substituted derivative against some bacterial strains and of the thienyl-substituted derivative against fungi were found to be similar to those of standard drugs.
机译:通过在冰醋酸中与各种取代的O-苯二胺反应合成了一系列新的取代的双苯并咪唑衍生物。 通过H-1和C-13 NMR,FT-IR和MS光谱阐明了新合成的化合物的结构,并评估了抗革兰氏阳性和革兰氏阴性细菌和抗真菌活性的抗微生物活性。 噻吩基取代的衍生物对芽孢杆菌的嗜睡症显示出显着的活性。 枯草芽孢杆菌,金黄色葡萄球菌,Klebsiella肺炎(细菌)和镰刀菌(真菌)。 发现氟取代的取代衍生物与某些细菌菌株和对真菌的噻吩基取代的衍生物的活性类似于标准药物的活性。

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