http://jcps.bjmu.edu.cn

• 简 报 • 上一篇    下一篇

新型3-草酰胺-2-苯基吲哚衍生物的合成及其黄体细胞生长抑制活性的研究

王浩, 闻韧*, 蒋为群, 董肖椿, 黄磊, 李宁, 曹霖   

  1. 1.复旦大学药学院合成药化教研室, 上海 200032;
    2.中国科学院上海药物研究所, 上海 200031
  • 收稿日期:2000-09-15 修回日期:2000-12-20 出版日期:2001-03-15 发布日期:2001-03-15
  • 通讯作者: 闻韧*

Synthesis of Several 3-Oxamoyl-2-phenylindole Derivatives and Their Ability to Inhibit on Cultured Rat Luteal Cell Growth

Wang Hao, Wen Ren*, Jiang Weiqun, Dong Xiaochun, Huang Lei, Li Ning, Cao Lin   

  1. 1. Department of Medicinal Chemistry, Fudan University, Shanghai 200032;
    2. Department of Pharmacology, Shanghai Institute of Materia Medica, Shanghai 200031
  • Received:2000-09-15 Revised:2000-12-20 Online:2001-03-15 Published:2001-03-15
  • Contact: Wen Ren*

摘要: 本文报道以苯肼为原料合成了62-苯基-3-草酰胺基吲哚衍生物1a~f, 其结构均未见文献报道。经初步体外试验结果表明, 所被测试的6个目标化合物均具一定的离体黄体细胞生长抑制活性, 2-(4-甲氧苯基)吲哚化合物1b~d的活性明显高于2-苯基吲哚化合物1a。但在1b的吲哚氮上引入甲基或异丙基对活性没有影响。

关键词: 3-草酰胺-2-苯基吲哚, 黄体细胞生长抑制, 合成

Key words: Oxamoyl-2-phenylindole, Luteal cell growth's inhibition, Synthesis

Supporting: *Supported by National Natural Science Foundation of China (No 29872029), National Health Ministry Foundation of China (No 941184) and Shanghai Municipal Education Committee Key Discipline Foundation (No 98-12).