中國醫藥大學機構典藏 China Medical University Repository, Taiwan:Item 310903500/24095
English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 29490/55136 (53%)
造訪人次 : 1559768      線上人數 : 274
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋
    主頁登入上傳說明關於CMUR管理 到手機版
    請使用永久網址來引用或連結此文件: http://ir.cmu.edu.tw/ir/handle/310903500/24095


    題名: 合成FIT-OH及AVLPR-OH類緣化合物作為細胞分化劑與有絲分裂抑制劑;Synthesis of FIT-OH and AVLPR-OH analogs as cell differentiation agents and antimitotic agents
    作者: 劉玉晴;Yu-Ching Liu
    貢獻者: 中國醫藥學院藥物化學研究所
    關鍵詞: 細胞分化劑;有絲分裂抑制劑;固相peptide合成;分子模擬;cell differentiation agents;antimitotic agents;Solid Phase Peptide Synthesis;Molecular Modeling
    日期: 1990
    上傳時間: 2009-12-03 09:29:39 (UTC+8)
    摘要: 延續針對更強的細胞分化劑之研究中,選擇以AVLPR-OH為先導化合物做結構上的修飾。另一方面,由分子模擬設計一系列FIT-OH類緣化合物做為有絲分裂抑制劑。 標的化合物的合成以標準的固相peptide合成方法,針對peptide acids (TP-1, TP-3~TP-11及PP-1)之合成用Fmoc-Amino acid-Wang resin,而對於peptide amides (TP-2, PP-2及PP-3)之合成用Rink resin;合成之產物由逆相-高效液相層析法純化,繼而分子量由FAB-MS確認。; As part of our continuing search for potential cell differentiation agents, AVLPR-OH was selected as the lead compound for structural modification. On the other hand, a series of FIT-OH analogs was designed as antimitotic agents by Molecular Modeling. The target compounds were synthesized on Fmoc-Amino acid-Wang resin for peptide acids (TP-1, TP-3 — TP-11 and PP-1), and Rink resin for peptide amides (TP-2, PP-2 and PP- 3), by standard Solid Phase Peptide Synthesis. Each of synthesized products were purified by RP-HPLC and their molecular weight were confirmed by FAB-MS.
    顯示於類別:[藥物化學研究所] 博碩士論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    index.html0KbHTML178檢視/開啟


    在CMUR中所有的資料項目都受到原著作權保護.

    TAIR相關文章

     


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回饋