• DocumentCode
    2478560
  • Title

    Lipid lowering activity of (E)-3-[4-[2-(4-chlorophenoxy)-2-methylpropanoylox y]-3-methoxyphenyl] acrylic acid (AZ) in hyperlipidemic rats

  • Author

    Chen, Xiao-Bing ; Xu, Jun ; Zhao, Po ; Yang, Zun-Hua ; Peng, Hong

  • Author_Institution
    Lab. for Pharmacochemistry, JiangXi Univ. of Traditional Chinese Med., Nanchang, China
  • fYear
    2011
  • fDate
    24-26 June 2011
  • Firstpage
    7664
  • Lastpage
    7667
  • Abstract
    Hyperlipidemia is closely related to Cardiovascular Disease, and also an important risk factor to affect Atherosclerosis, Coronary Heart Disease (CHD) and other Cardiovascular Disease. And hyperlipidemia could severely affect the health of human. In order to find better biological activity of lowering blood-lipids, we introduced the target compound of AZ. The lead compound were designed and synthesized by chlorophenoxy isobutyric acid of chemical lowering blood-lipid drugs and ferulic acid which is traditional Chinese medicine active products. The structure of the target compound prepared were confirmed by IR,MS, 1H-NMR,and elemental analysis. The herbicidal results show that the target compound has good lowering hyperlipidemia activities.
  • Keywords
    cardiovascular system; diseases; drugs; organic compounds; (E)-3 [4[2-(4-chlorophenoxy )-2-methy lpropanoy loxy]-3-methoxyphenyl] acrylic acid; atherosclerosis; cardiovascular disease; chlorophenoxy isobutyric acid; coronary heart disease; drugs; ferulic acid; hyperlipidemia; hyperlipidemic rats; lipid lowering activity; risk factor; traditional Chinese medicine; Atherosclerosis; Biological system modeling; Blood; Compounds; Drugs; Lipidomics; Rats; Biological activities; Esterification; Hyperlipidemia; Synthesis;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Remote Sensing, Environment and Transportation Engineering (RSETE), 2011 International Conference on
  • Conference_Location
    Nanjing
  • Print_ISBN
    978-1-4244-9172-8
  • Type

    conf

  • DOI
    10.1109/RSETE.2011.5966150
  • Filename
    5966150