应用化学 ›› 2017, Vol. 34 ›› Issue (7): 783-788.DOI: 10.11944/j.issn.1000-0518.2017.07.160440

• 研究论文 • 上一篇    下一篇

溴代甲氧基二苯甲酮咪唑类化合物的合成及对过氧化氢致EA.hy 926细胞损伤的保护作用

宋婷,孔德朋,王勤金,冯秀娥(),李青山   

  1. 山西医科大学药学院 太原 030001
  • 收稿日期:2016-11-03 接受日期:2017-01-23 出版日期:2017-07-04 发布日期:2017-07-04
  • 通讯作者: 冯秀娥
  • 基金资助:
    国家高技术研究发展计划(“863”计划)(2013AA092903);国家自然科学基金(81473100);2014年度山西省煤基重点科技攻关项目(MJH2014-14);山西医科大学博士启动基金资助项目(B03201213)

Synthesis of Bromo-Methoxyl Benzophenone Imidazole Compounds and Their Protective Activities Against Hydrogen Peroxide Induced Injury in EA.hy 926 Cells

SONG Ting,KONG Depeng,WANG Qinjin,FENG Xiu'e(),LI Qingshan   

  1. School of Pharmaceutical Science,Shanxi Medical University,Taiyuan 030001,China
  • Received:2016-11-03 Accepted:2017-01-23 Published:2017-07-04 Online:2017-07-04
  • Contact: FENG Xiu'e
  • Supported by:
    Supported by the National High Technology Research and Development Plan(“863” plan)(No.2013AA092903), the National Natural Science Foundation of China(No.81473100, Shanxi Province Coal-based Key Scientific and Technological Projects in 2014(No.MJH2014-14), Ph.D.Funded Start-up Funding of Shanxi Medical University(No.B03201213)

摘要:

本文旨在引入咪唑环,对溴代甲氧基二苯甲酮类化合物进行结构衍生,以发现对血管内皮细胞具有更高保护活性的化合物。 通过以2-甲基-5-溴-苯甲酸为起始原料,经过酰氯化、傅克酰化、溴代、与N-溴代丁二酰亚胺(NBS)自由基取代及与取代咪唑的亲核取代等多步反应,合成了8个新型溴代甲氧基二苯甲酮咪唑类化合物。 目标化合物的结构均经质谱(MS)、核磁共振波谱仪(NMR)和高分辨质谱(HRMS)进行确证。 并采用噻唑蓝(MTT)法考察了目标化合物对过氧化氢损伤的EA.hy 926细胞的保护活性,结果表明,目标化合物6a、6g、6h具有显著的细胞保护活性,其半抑制浓度(EC50)分别为1.9、4.0和3.2 μmol/L,优于阳性对照槲皮素(EC50为18 μmol/L),表明该类化合物在心血管疾病的治疗方面有潜在的应用前景。

关键词: 溴代甲氧基二苯甲酮, 咪唑, EA.hy 926细胞, 保护活性

Abstract:

To introduce the imidazole ring to the bromo-methoxyl benzophenone structures and find the target compounds with high protective activity on vacular endothelium cells, eight novel bromo-methoxyl benzophenone imidazole compounds were synthesized using 5-bromo-2-methylbenzoic acid as starting material via following reactions:acylating chlorination, Friedel acylation, bromination, radical substitution with N-bromosuccinimide(NBS) and nucleophilic substitution with substituted imidazoles. The structures of the target compounds were confirmed by proton and carbon nuclear magnetic resonance spectroscopy(1H and 13C NMR) and high resolution mass spectrometry(HRMS). Additionally, the protective effects of the target compounds against H2O2-induced EA.hy 926 cells injury were evaluated by methylthiazolyldiphenyl-tetrazolium bromide(MTT) assay and their structure-activity relationships were also preliminarily discussed. The in vitro results show that target compounds 6a, 6g and 6h exhibit significant cytoprotective activities and their half maximal inhibitory concentration(EC50) values are 1.9, 4.0 and 3.2 μmol/L, respectively, superior to the positive control Quercetin(EC50≈18 μmol/L). These results also suggest the potential application prospect of target compounds in the treatment of cardiovascular diseases.

Key words: bromo-methoxyl benzophenone, imidazole, EA.hy 926 cells, protective activity