Taipei Medical University Institutional Repository:Item 987654321/51087
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 45422/58598 (78%)
Visitors : 2546182      Online Users : 244
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU 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: http://libir.tmu.edu.tw/handle/987654321/51087


    Title: Study of Phytochemistry and Bioactivity of Constituents from Fruits of Aquilaria crassna
    Authors: GAYATHRI.UPPALA
    Keywords: Aquilaria crassna;antiglycemic;sesquiterpenoids;thymelaeaceae;iriflophenone 2-O-α-rhamnopyranoside;4-hydroxybenzoic acid;mangnferin;rhamnocitrin-3-O-β-D-glucoside;kaempferol-3-(6-coumaroyl)-glucoside
    Date: 2013-07-05
    Issue Date: 2018-10-05 11:53:33 (UTC+8)
    Abstract: The resinous portions of Aquilaria plants, called Aquilaria crassna, have been used as medicines and incenses. It contains a great variety of sesquiterpenes. This oil is widely used among various countries as perfumes and ingredient in medical recipes. The present study aims to analyze the phytochemistry of medicinal plant, Aquilaria crassna fruit. The specific objectives of the study are to extract A.crassna by using 100% methanol and to isolate the compounds using open column, and medium pressure liquid chromatography (MPLC) methods. In addition to this, the study has also been conducted to elucidate the structures of isolated pure compounds using nuclear magnetic resonance spectroscopic techniques.
    The research was designed with an experimental method. The dried A.crassna (6.13 kg) was extracted three times by 100% MeOH, at room temperature after 3 days. Pure compounds were isolated from MeOH extract using various column chromatographical techniques.
    The elucidated pure compounds from ethyl acetate layer were identified to be iriflophenone 2-O-α-rhamnopyranoside (1),4-hydroxybenzoic acid (2), mangiferin (3), rhamnocitrin-3-O-β-D-glucoside (4) kaempferol-3-(6′-coumaroyl) glucoside (5). The structures of these compounds were determined by extensive spectroscopic analyses, including 1D and 2D NMR.
    Description: 碩士
    指導教授-徐鳳麟
    委員-張永勳
    委員-盧美光
    委員-李美賢
    委員-吳姿樺
    Data Type: thesis
    Appears in Collections:[Graduate Institute of Pharmacognosy Science] Dissertation/Thesis

    Files in This Item:

    File Description SizeFormat
    index.html0KbHTML350View/Open


    All items in TMUIR are protected by copyright, with all rights reserved.


    著作權聲明 Copyright Notice
    • 本平台之數位內容為臺北醫學大學所收錄之機構典藏,包含體系內各式學術著作及學術產出。秉持開放取用的精神,提供使用者進行資料檢索、下載與取用,惟仍請適度、合理地於合法範圍內使用本平台之內容,以尊重著作權人之權益。商業上之利用,請先取得著作權人之授權。

      The digital content on this platform is part of the Taipei Medical University Institutional Repository, featuring various academic works and outputs from the institution. It offers free access to academic research and public education for non-commercial use. Please use the content appropriately and within legal boundaries to respect copyright owners' rights. For commercial use, please obtain prior authorization from the copyright owner.

    • 瀏覽或使用本平台,視同使用者已完全接受並瞭解聲明中所有規範、中華民國相關法規、一切國際網路規定及使用慣例,並不得為任何不法目的使用TMUIR。

      By utilising the platform, users are deemed to have fully accepted and understood all the regulations set out in the statement, relevant laws of the Republic of China, all international internet regulations, and usage conventions. Furthermore, users must not use TMUIR for any illegal purposes.

    • 本平台盡力防止侵害著作權人之權益。若發現本平台之數位內容有侵害著作權人權益情事者,煩請權利人通知本平台維護人員([email protected]),將立即採取移除該數位著作等補救措施。

      TMUIR is made to protect the interests of copyright owners. If you believe that any material on the website infringes copyright, please contact our staff([email protected]). We will remove the work from the repository.

    Back to Top
    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback