首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Synthesis and Biological Activities of 2-[3-(4-Morpholino)propyIthio]-5-(difluromethoxy)benzimidazole Derivatives
【24h】

Synthesis and Biological Activities of 2-[3-(4-Morpholino)propyIthio]-5-(difluromethoxy)benzimidazole Derivatives

机译:2- [3-(4-Morpholino)丙基硫代] -5-(二氟甲氧基)苯并咪唑衍生物的合成及生物活性

获取原文
获取原文并翻译 | 示例
       

摘要

Benzimidazple derivatives exhibit some important pharmacological actions in animals and human beings. The synthesis and pharmacological effects of two novel synthesized compounds, 2-{3-(4-morpnolino)propylthio]- 5-(difiuromethoxy)benzimidazole (BM1) and 2-[3-(4-morpholino)ethylthio]-5-(diflurometboxy)benzimidazole (BM2), were described in this work. The tests showed that BM1 had better antiinflammatory effect than aspirin and better analgesia activity than indomethacin, while these two compounds had lower side effect of gastric Ulcer than aspirin. Therefore, BM1 was an ideal antiinflammatory compound for further development.
机译:苯并咪唑衍生物在动物和人类中表现出一些重要的药理作用。两种新型合成化合物2- {3-(4-morpnolino)propylthio]-5-(difiuromethoxymethoxy)benzimidazole(BM1)和2- [3-(4-morpholino)ethylthio] -5-(在这项工作中描述了二氟苄基)苯并咪唑(BM2)。试验表明,BM1的抗炎作用比阿司匹林好,镇痛活性比消炎痛好,而这两种化合物的胃溃疡副作用比阿司匹林低。因此,BM1是进一步发展的理想抗炎化合物。

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