期刊文献+

姜黄素衍生物的合成及抑菌活性研究 被引量:5

Preparation and Antimicrobial Activities of Curcumin Derivatives
暂未订购
导出
摘要 以含有杂原子的生物素、硫辛酸、异烟酸和姜黄素为原料,以二步酰氯法合成了姜黄素生物素酯、姜黄素硫辛酸酯、姜黄素异烟酸酯。经红外,核磁共振氢谱和质谱确证了化合物的结构。在相同条件下,以姜黄素为对照测定了产物对金色葡萄球菌的抑菌性能。结果显示,姜黄素硫辛酸酯、姜黄素生物素酯、姜黄素异烟酸酯三种姜黄素衍生物在抑菌活性上均有不同程度的增强,最小抑菌浓度(MIC)分别为2.5、5.0、5.0 mg/mL,在最小抑菌浓度下抑菌圈分别为10、10、8 mm。 Curcumin derivatives were synthesized with biotin, lipolic acid, isonicotlnic acid and curcumin, using the acylchloride method. Their chemical structures were confirmed by IR, MS and 1H-NMR spectroscopy. The antimicrobial activities of these new compounds were explored with Staphylicoccus aureus under the same conditions compared with cur- cumin. The results showed that the antimicrobial activities of these new compounds were better than curcumin, the MICs were 2.5,5.0,5.0 mg/mL. The diameters of inhibition zone of each products were 10,10,8 mm.
出处 《天然产物研究与开发》 CAS CSCD 北大核心 2013年第2期237-240,共4页 Natural Product Research and Development
基金 山东省自然科学基金项目(ZR2010BM021)
关键词 生物素姜黄素酯 硫辛酸姜黄素酯 异烟酸姜黄素酯 金色葡萄球菌 抑菌活性 biotin curcumin ester lipoic curcumin ester isonicotinic curcumln ester Staphylicoccu aureua antimicrobialactivities
  • 相关文献

参考文献9

  • 1Forst-Ludwig A, Neumann M, Schneider-Brachert W, et al. Cureumin blocks NF-KB and the motogenie response in Heli- eobacter pylori-infeeted epithelial cells. Biochem Biophys Res Commun,2004,316 : 1065-1072.
  • 2Selvam C, Jachak SM, Thilagavathi R, et al. Design, synthe- sis, biological evaluation and molecular docking of curcumin analogues as antioxidant,cyclooxygenase inhibitory and anti- inflammatory agents. Bioorg Med Chem Lett , 2005,15 : 1793- 1797.
  • 3Mishra S, Karmodiya K, Surolia N,et al. Synthesis and explo- ration of novel eurcumin analogues as anti-malarial agents. Bioorg Med Chem ,2008 ,16 : 2894-2902.
  • 4胡玉梅,熊亮,黄涛,刘浩文,刘惠玲.硫辛酰胺的合成与表征[J].中南民族大学学报(自然科学版),2008,27(4):13-15. 被引量:2
  • 5何黎琴,王效山,罗丹.姜黄素烟酸酯的合成[J].化学世界,2011,52(3):175-177. 被引量:9
  • 6黄淑芳,应华洲,胡永洲.含氮姜黄素衍生物的合成及抗肿瘤活性研究[J].中国药物化学杂志,2011,21(2):88-95. 被引量:8
  • 7YahCH(颜成虎)Biofunctionalization of polylactide-poly-ethylene glycol (PLA-PEG) nanoparticles for targeting tob brainglioma.Tianjin:TianjinUniversity(天津大学),MSc.2007.
  • 8钟英英,黄晓畅,陈世益.姜黄素的体外抑菌活性研究[J].安徽农业科学,2010,38(34):19369-19370. 被引量:15
  • 9Kim K.I, Yu HH, Cha JD, et al. Antibacterial activity of cur- cuma longa L. against methicillin-resistant Staphylococcus au- reus. Phytother Res ,2005 ,19 : 599-604.

二级参考文献31

  • 1汤春芳,刘云国,徐卫华,李程峰.硫辛酸的研究概况[J].中国生化药物杂志,2005,26(1):52-55. 被引量:49
  • 2陈仕江,丁伟,杨帮,吴孝波.10种中药植物杀菌活性研究[J].重庆中草药研究,2004(2):1-4. 被引量:9
  • 3黄涛,黄开勋.硫辛酰苯并三唑的合成及反应活性[J].化学与生物工程,2005,22(8):25-27. 被引量:1
  • 4卢新军,蒋和体.姜黄素生理功能及其在食品工业中的应用前景[J].中国食物与营养,2006,12(4):31-32. 被引量:19
  • 5洪广峰,张建业,白延海,陶建中,李瑞军.α-硫辛酸的合成工艺改进[J].河南化工,2006,23(5):19-20. 被引量:1
  • 6Szabados E, Fischer G M, Gallyas F, et al. Enhanced ADP-ribosylation and its diminution by lipoamide after ischemia-reperfusion in perfused rat heart. Free Radical Biology and Medicine[J].1999, 27 (9-10): 1 103-1 113.
  • 7Elliott J D, Steele J, Johnson W S. An efficient asymmetric synthesis of R (+)-α-lipoic acid [J]. Tetrahedron Lett , 1985, 26 (21) : 2 535 - 2 538.
  • 8Chavan S P, Shivsankar K, Pasupathy K. Simplistic expedient and practical synthesis of (±)-α-lipoic acid [J]. Synthesis, 2005(8):1 297-1 300.
  • 9徐亚明,李志田,顾云龙.硫辛酰胺新合成方法[P].CN,96116303.8,1997-10-08.
  • 10ARATANECHEMUGEI Y,KOMIRAI T,MOTEKI H,et a1.Selective induction of apoptosis by ar-turmerone isolated from turmeric(Cureuma longs L)in two human leukemia cell lines,but not in human stomach cancer cell line[J].Inter J of Mol Med,2002(9):481-484.

共引文献30

同被引文献44

引证文献5

二级引证文献40

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部