English  |  正體中文  |  简体中文  |  Items with full text/Total items : 62819/95882 (66%)
Visitors : 4010875      Online Users : 958
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library & TKU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/112608


    Title: Isolation and identification of novel α-amylase inhibitors from Euonymus laxiflorus Champ
    Authors: Nguyen VB;Wang SL;Nguyen AD;Vo TPK;Zhang LJ;Nguyen QV;Kuo YH
    Keywords: α-amylase inhibitor;Euonymus laxiflorus Champ.;Medicinal plants;Diabetes;Obesity;Bioactive compounds
    Date: 2018
    Issue Date: 2018-01-24 02:10:19 (UTC+8)
    Publisher: Springer
    Abstract: Euonymus laxiflorus Champ. (ELC) has been reported to possess potential
    antidiabetic activity. The aim of this study is to isolate and identify the active
    compounds in ELC extract. Application of effective techniques including Diaoin,
    octadecylsilane opened columns, dialysis, and preparative high-performance liquid
    chromatography (HPLC) coupled with a biologically guided assay resulted in isolation
    of 11 novel active compounds. Five compounds were identified as new α-amylase inhibitors (αAIs), viz. walterolactone A/B β-D-pyranoglucoside (1),
    schweinfurthinol 9-O-β-D-pyranoglucoside (10), 1-O-(3-methyl)-butenoyl-myoinositol (11), leonuriside (13), and (3,5-dimethoxy-4-hydroxyphenol) -1-O-β-D-(6′-O-galloyl)-glucopyranoside (21). Among these inhibitors, three compounds (1, 10, 11) were characterized as new. Another six known compounds (2, 9, 16, 17, 18, 19) were determined as phenolic. Notably, six compounds (1, 2, 9, 13, 16, 17) demonstrated significant activity, comparable to or higher than that of acarbose, a commercial antidiabetic drug, based on t test ranking. The relationship between the chemical structures and bioactivity of the inhibitors is also reported.
    Relation: Research on Chemical Intermediates 44(2), p.1411-1424
    Appears in Collections:[Graduate Institute & Department of Chemistry] Journal Article

    Files in This Item:

    File Description SizeFormat
    index.html0KbHTML2View/Open
    index.html0KbHTML183View/Open
    Isolation and identification of novel α-amylase inhibitors from Euonymus laxiflorus Champ.pdf639KbAdobe PDF2View/Open

    All items in 機構典藏 are protected by copyright, with all rights reserved.


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library & TKU Library IR teams. Copyright ©   - Feedback