Synthesis and biological evaluation of tetrahydroisoquinoline derivatives as potential multidrug resistance reversal agents in cancer

Yu Li Hui Bin Zhang Wen Long Huang Xia Zhen Yun Man Li

引用本文: Yu Li,  Hui Bin Zhang,  Wen Long Huang,  Xia Zhen,  Yun Man Li. Synthesis and biological evaluation of tetrahydroisoquinoline derivatives as potential multidrug resistance reversal agents in cancer[J]. Chinese Chemical Letters, 2008, 19(2): 169-171. doi: 10.1016/j.cclet.2007.12.016 shu
Citation:  Yu Li,  Hui Bin Zhang,  Wen Long Huang,  Xia Zhen,  Yun Man Li. Synthesis and biological evaluation of tetrahydroisoquinoline derivatives as potential multidrug resistance reversal agents in cancer[J]. Chinese Chemical Letters, 2008, 19(2): 169-171. doi: 10.1016/j.cclet.2007.12.016 shu

Synthesis and biological evaluation of tetrahydroisoquinoline derivatives as potential multidrug resistance reversal agents in cancer

  • 基金项目:

    The work was supported by the Hi-tech Research and Development Program of China (No. 2002AA233071).

摘要: Tetrahydroisoquinoline derivatives were synthesized and their multidrug resistance reversal activities were evaluated in vitro.The results showed that some of the synthetic compounds had higher multidrug resistance (MDR) reversal activities than verapamil.

English

  • 加载中
计量
  • PDF下载量:  1
  • 文章访问数:  786
  • HTML全文浏览量:  37
文章相关
  • 收稿日期:  2007-10-22
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

/

返回文章