首页> 外文期刊>Journal of Drug Delivery and Therapeutics >Synthesis and Biological Evaluation of Some Piperazine Derivatives as Anti-Inflammatory Agents
【24h】

Synthesis and Biological Evaluation of Some Piperazine Derivatives as Anti-Inflammatory Agents

机译:某些哌嗪衍生物作为抗炎剂的合成及生物学评价

获取原文
           

摘要

Some 1-((4-methylpiperazin-1yl)methyl)-1H-benzo[d]imidazole & 1-((4-phenylpiperazin-1yl)methyl)-1H-benzo[d]imidazole derivatives were synthesized through reaction of 1-substituted piperazines with different benzimidazole derivatives in methanol yielded the corresponding mannich bases (42-a to 42-i). All the synthesized compounds were elucidated by IR, sup1/supH NMR and MASS spectroscopy. They were tested for anti-inflammatory activity using in-vivo (Carrageenan- induced rat paw edema model) method at a dose of 50mg/kg. result showed that compounds 42-c, 42-d and 42-h were found to be most potent in series.
机译:通过1-的反应合成了一些1-(((4-甲基哌嗪-1基)甲基)-1H-苯并[d]咪唑和1-((4-苯基哌嗪-1基)甲基)-1H-苯并[d]咪唑衍生物在甲醇中用不同的苯并咪唑衍生物取代的哌嗪产生相应的曼尼希碱(42-a至42-i)。通过IR, 1 1 H NMR和MASS光谱对所有合成的化合物进行了阐明。使用体内(角叉菜胶诱导的大鼠爪水肿模型)方法以50mg / kg的剂量测试它们的抗炎活性。结果表明,化合物42-c,42-d和42-h的串联作用最强。

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