首页> 外文期刊>Anti-Inflammatory & Anti-allergy Agents in Medicinal Chemistry >Novel 2-(nitrooxy)ethyl 2-(4-(substituted phenyl)-2-((substituted phenyl)amino)thiazol-5-yl)acetate as Anti-inflammatory, Analgesic and Nitric Oxide Releasing Agents: Synthesis and Molecular Docking Studies
【24h】

Novel 2-(nitrooxy)ethyl 2-(4-(substituted phenyl)-2-((substituted phenyl)amino)thiazol-5-yl)acetate as Anti-inflammatory, Analgesic and Nitric Oxide Releasing Agents: Synthesis and Molecular Docking Studies

机译:新型2-(硝基氧基)乙基2-(4-(取代的苯基)-2-((取代的苯基)氨基)噻唑-5-基)作为抗炎,镇痛和一氧化氮释放剂:合成和分子对接研究

获取原文
获取原文并翻译 | 示例
           

摘要

Background'. Due to the need and adverse effects associated with the available anti-inflammatory agents, an attempt was made to develop the new anti-inflammatory agents with better activity and lesser adverse effects. Objective: Synthetic approaches based on chemical modification of NSAIDs have been undertaken with the aim of improving NSAIDs safety profile. Method'. In the present study, a series of thiazole derivatives (3a-3x) was synthesized and tested for its anti-inflammatory with analgesic and nitric oxide releasing properties. In this work, synthesis of molecules containing substituted diaryl ring on 5-membered thiazole ring with nitric oxide releasing moiety is described. Results'. Out of the twenty four synthesized compounds, five compounds showed considerable anti-inflammatory and analgesic activity in comparison with the standard. Most of the synthesized compounds showed considerable nitric oxide-releasing property. The molecular docking study was used to rationalize binding interaction at the active site and the result showed good binding interaction. Conclusion: From the results of pharmacological studies, we conclude that the synthesized compounds have not only retained, but showed enhanced anti-inflammatory and analgesic profile.
机译:背景'。由于与可用的抗炎剂相关的需要和不利影响,试图开发具有更好活性和较小的不良反应的新型抗炎剂。目的:基于NSAID的化学改性的合成方法,目的是改善NSAIDS安全性剖面。方法'。在本研究中,合成了一系列噻唑衍生物(3A-3X)并测试其抗炎,镇痛和一氧化氮释放性能。在这项工作中,描述了在5-元噻唑环上含有取代的二芳基环的分子的合成,其具有一氧化氮释放部分。结果'。除了二十四种合成化合物中,与标准相比,五种化合物显示出相当大的抗炎和镇痛活性。大多数合成化合物显示出相当大的一氧化氮释放性。分子对接研究用于在活性位点合理化结合相互作用,结果显示出良好的结合相互作用。结论:从药理研究结果中,我们得出结论,合成化合物不仅保留,而且显示出增强的抗炎和镇痛概况。

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