Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/24235
English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 18076/20274 (89%)
造訪人次 : 5301238      線上人數 : 1018
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
    請使用永久網址來引用或連結此文件: https://ir.cnu.edu.tw/handle/310902800/24235


    標題: Synthesis and Inhibition of RANKL-induced Osteoclastogensis of Indeno [1,2-c] quinoline Derivatives
    作者: You-Ren Chen (陳宥任)
    Chih-Hua Tseng (曾志華)
    Chiao-Li Yang (楊巧麗)
    Yeh-Long Chen (陳義龍)
    Cherng-Chyi Tzeng (曾誠齊)
    日期: 2011
    上傳時間: 2011-06-23 14:57:24 (UTC+8)
    摘要: Certain indeno[l,2-c]quinolines were synthesized and evaluated for anti-osteoclastogenic activities. Among them, 6,9-dimethoxy-11H-indeno[l,2-c]- quinolin-11 -one (8a) and 9-methoxy-6-(methylthio)-11H-indeno[ 1,2-c] quinolin-11 -one (16a) inhibited RANKL-induced osteoclast formation in Raw 264.7 cells with an IC50 of 2.00 and 2.58 M respectively. Compound 8a was only weekly active in the inhibition of the RANKL-induced NFAT activation while 16a was inactive. These results indicated that the anti-osteoclastogenic effect of 8a is only partly related while 16a is not related to the suppression of NFAT.
    關聯: 2011年台俄有機、藥物與生物化學交流暨藥物化學研討會,起迄日:2011/04/06~2011/04/05,地點:溪頭台大實驗林
    顯示於類別:[藥理學院] 2011年台俄有機、藥物與生物化學交流暨藥物化學研討會

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    pp-19.pdf50KbAdobe PDF428檢視/開啟


    在CNU IR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