English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 29490/55136 (53%)
造訪人次 : 1496628      線上人數 : 428
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/310903500/7638


    題名: Cytotoxicity of phenylpropanoid esters from the stems of Hibiscus taiwanensis
    Cytotoxicity of phenylpropanoid esters from the stems of Hibiscus taiwanensis
    作者: 吳培琳(Pei-Lin Wu);莊大賢(Ta-Hsien Chuang);賀彩霞(Cai-Xia He);吳天賞(Tian-Shung)*
    貢獻者: 藥學院藥學系
    關鍵詞: Malvaceae;Hibiscus taiwanensis;Lignan;9,9′-O-feruloyl-(−)-secoisolaricinresinol
    Malvaceae;Hibiscus taiwanensis;Lignan;9,9′-O-feruloyl-(−)-secoisolaricinresinol
    日期: 2004-05
    2004-05
    上傳時間: 2009-08-26 16:32:08 (UTC+8)
    2009-08-26 16:32:08 (UTC+8)
    摘要: The separation of an extract prepared from the stems of the previously uninvestigated Hibiscus taiwanensis led to the isolation of three new phenylpropanoid esters, (7S,8S)-demethylcarolignan E (1), hibiscuwanin A (2), hibiscuwanin B (3), in addition to eight known ones. The structures of these compounds were elucidated by spectroscopic and chemical transformation studies. In cytotoxicity evaluation of the isolates, 9,9′-O-feruloyl-(−)-secoisolaricinresinol (8) showed strong cytotoxic activity against human lung carcinoma and breast carcinoma cell lines in an in vitro cytotoxicity assay with EC50 values of 1.8 and 3.9 μg/mL, respectively.

    Three new phenylpropanoid esters, (7S,8S)-demethylcarolignan E (1), hibiscuwanin A (2), hibiscuwanin B (3), in addition to eight known ones were isolated from the stems of Hibiscus taiwanensis. Among those isolates, 9,9′-O-feruloyl-(−)-secoisolaricinresinol (8) showed strong cytotoxic activity against human lung carcinoma and breast carcinoma cell lines with EC50 values of 1.8 and 3.9 μg/mL, respectively.
    The separation of an extract prepared from the stems of the previously uninvestigated Hibiscus taiwanensis led to the isolation of three new phenylpropanoid esters, (7S,8S)-demethylcarolignan E (1), hibiscuwanin A (2), hibiscuwanin B (3), in addition to eight known ones. The structures of these compounds were elucidated by spectroscopic and chemical transformation studies. In cytotoxicity evaluation of the isolates, 9,9′-O-feruloyl-(−)-secoisolaricinresinol (8) showed strong cytotoxic activity against human lung carcinoma and breast carcinoma cell lines in an in vitro cytotoxicity assay with EC50 values of 1.8 and 3.9 μg/mL, respectively.

    Three new phenylpropanoid esters, (7S,8S)-demethylcarolignan E (1), hibiscuwanin A (2), hibiscuwanin B (3), in addition to eight known ones were isolated from the stems of Hibiscus taiwanensis. Among those isolates, 9,9′-O-feruloyl-(−)-secoisolaricinresinol (8) showed strong cytotoxic activity against human lung carcinoma and breast carcinoma cell lines with EC50 values of 1.8 and 3.9 μg/mL, respectively.
    關聯: BIOORGANIC & MEDICINAL CHEMISTRY 12(9 )2193 ~2197
    BIOORGANIC & MEDICINAL CHEMISTRY 12(9 )2193 ~2197
    顯示於類別:[藥學系暨碩博士班] 期刊論文

    文件中的檔案:

    檔案 大小格式瀏覽次數
    58KbUnknown485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