Skip navigation

DSpace JSPUI

DSpace preserves and enables easy and open access to all types of digital content including text, images, moving images, mpegs and data sets

Learn More
DSpace logo
English
中文
  • Browse
    • Communities
      & Collections
    • Publication Year
    • Author
    • Title
    • Subject
  • Search TDR
  • Rights Q&A
    • My Page
    • Receive email
      updates
    • Edit Profile
  1. NTU Theses and Dissertations Repository
  2. 理學院
  3. 化學系
Please use this identifier to cite or link to this item: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/40347
Title: 設計及合成類黃酮配醣體做為RPE細胞抗氧化試劑
Synthesis of Flavonoid C-Glycosides as Antioxidants for Protection of Retinal Pigment Epithelial Cells
Authors: Chih-An Chen
陳志安
Advisor: 方俊民(Jim-Min Fang)
Keyword: 視網膜色素上皮細胞,類黃酮,抗氧化,
Retinal Pigment Epithelial Cells,Flavonoid,Antioxidants,
Publication Year : 2008
Degree: 碩士
Abstract: 視網膜色素上皮細胞層 (retinal pigment epithelium, RPE) 位於眼睛的後方,厚度只有一層,排列在布魯赫氏膜與光接受器之間。RPE功能眾多,主要有光線吸收、維生素A的儲存與運送、供給感光細胞氧氣和養份,及沉澱廢物的清除。RPE會隨著年齡的增加而死亡或游離至他處,RPE功能退化會引發一些視網膜疾病,常見的有,增殖性視網膜病變 (proliferative vitreoretinopathy), 糖尿病所引發的視網膜血管新生 (proliferative diabetic retinopathy),老年性黃斑部病變 (aged-macular degeneration, AMD)等,都與RPE細胞的機能息息相關。
石斛為蘭科植物,是重要的常用中藥,霍山石斛 (Dendrobium huoshanense) 為石斛種類中之上品,原產於中國安徽霍山等地,與靈芝、冬蟲夏草並列為中國三大珍貴靈草。根據古方與相關研究報告,石斛藥用廣泛,除了具有「清肝明目」療效,也有抗衰老、抗腫瘤、治療白內障、提高身體免疫力的功能。
從霍山石斛中分離出活性小分子—芹菜素配醣體具有「明目」療效,我們希望藉由化學合成方法來彌補霍山石斛天然物資源的缺乏,合成一系列芹菜素衍生物,搭配生物活性分析,篩選出最佳的活性分子,進而推測其藥效基團,並探討結構
A variety of C-glycosylflavonoids are found widely distributed in the plant kingdom. Dendrobium huoshanense is a well-known traditional Chinese medicine. Apigenin 6,8-di-C-glycosides have been suggested to exist in D. huoshanense to exhibit an activity for eye protection. Because the structure of the chemical constituent and the biological mechanism were unclear, we aim to synthesize a series of apigenin 6,8-di-C-glycosides and analogues for the structure–activity relationship study.
A key reaction was carried out by using Sc(OTf)3 as the promoter to furnish the C-glycosylation on phloroacetophenone with unprotected saccharides. The key compound was further converted to mono- and di-C-glycosides of apigenin. In order to increase the diversity, different sugars (D-glucose, L-arabinose, D-xylose etc.), and phenols were used to synthesize the analogues.
URI: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/40347
Fulltext Rights: 有償授權
Appears in Collections:化學系

Files in This Item:
File SizeFormat 
ntu-97-1.pdf
  Restricted Access
4.43 MBAdobe PDF
Show full item record


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

社群連結
聯絡資訊
10617臺北市大安區羅斯福路四段1號
No.1 Sec.4, Roosevelt Rd., Taipei, Taiwan, R.O.C. 106
Tel: (02)33662353
Email: ntuetds@ntu.edu.tw
意見箱
相關連結
館藏目錄
國內圖書館整合查詢 MetaCat
臺大學術典藏 NTU Scholars
臺大圖書館數位典藏館
本站聲明
© NTU Library All Rights Reserved