应用化学

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新型苯基噻吩-2-基甲酮类化合物的合成及其对人脐静脉内皮细胞的保护活性

孔亮,冯秀娥*,高洁,李静,李青山*   

  1. (山西医科大学药学院 太原 030001)
  • 收稿日期:2013-12-23 修回日期:2014-03-05 出版日期:2014-09-04 发布日期:2014-09-04
  • 通讯作者: 李青山,教授; Tel/Fax:0351-4690322; E-mail:sxlqs2012@163.com; 研究方向:基于机制研究的药物设计合成
  • 基金资助:
    国家“863”计划项目(2013AA092903),山西省自然科学基金资助项目(2013011060-2),山西医科大学科技创新基金资助项目(01201116),山西医科大学博士启动基金资助项目(B03201213),山西省高等学校大学生创新创业训练项目(2013116)

Synthesis of Novel Phenyl(thiophen-2-yl)methanone Derivatives and Their Cytoprotective Activities Against H2O2-induced Injury in Human Umbilical Vein Endothelial Cells

KONG Liang, FENG Xiue*, GAO Jie, LI Jing, LI Qingshan*   

  1. (School of Pharmaceutical Science,Shanxi Medical University,Taiyuan 030001,China)
  • Received:2013-12-23 Revised:2014-03-05 Published:2014-09-04 Online:2014-09-04

摘要: 合成了13个具有新型结构的苯基(噻吩-2-基)甲酮类化合物,其中3个化合物(9b,10b,11b)未见文献报道,目标化合物的结构均经ESI-MS、1H NMR和13C NMR等技术手段进行了确证。 对H2O2诱导的人脐静脉内皮细胞(HUVECs)氧化损伤保护活性的结果显示,对位甲氧基以及两个氯原子取代的活性较好。 初步构效关系表明,苯基噻吩甲酮母环上取代基的位置、数目、类型是影响化合物活性的主要原因。

关键词: 苯基(噻吩-基)甲酮, 合成, 人脐静脉内皮细胞, 保护活性

Abstract: Thirteen phenyl(thiophen-2-yl)methanone derivatives were designed and synthesized by classic synthetic methods, in which compounds 9b, 10b and 11b are new. All target structures were confirmed by ESI-MS, 1H NMR and 13C NMR. Their in vitro cytoprotective activities against H2O2-induced injury on human umbilical vein endothelial cells(HUVECs) were tested. And the results show that p-methoxy groups and two chlorine atoms substituted on the phenyl ring express preferable protective activity. The preliminary structure-activity relationships results show that the position, number and type of substituents on the core structure have remarkable effects on protective activities against H2O2 induced injury on HUVECs.

Key words: phenyl(thiophen-yl)methanone, synthesis, human umbilical vein endothelial cells, cytoprotective activity

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