Acta Chimica Sinica ›› 2005, Vol. 63 ›› Issue (17): 1613-1620. Previous Articles     Next Articles

Original Articles

哌啶酮类法尼基转移酶抑制剂的设计、合成及初步抗肿瘤活性研究

葛燕丽,姜凤超*   

  1. (华中科技大学同济医学院药学院 武汉 430030)
  • 投稿日期:2004-12-08 修回日期:2005-05-29 发布日期:2010-12-10
  • 通讯作者: 姜凤超

Design, Synthesis and Antitumor Activity of Piperidone Inhibitors of Farnesyltransferase

GE Yan-Li,JIANG Feng-Chao*   

  1. (School of Pharmacy, Tongji Medical College of Huazhong University of Science and Technology, Wuhan 430030)
  • Received:2004-12-08 Revised:2005-05-29 Published:2010-12-10
  • Contact: JIANG Feng-Chao

he hypothesis of piperidone inhibitors of farnesyltransferase was built with the computer-aided drug design software—Catalyst. According to the hypothesis and structure-activity relationship of piperidone inhibitors, 17 novel piperidone inhibitors of farnesyltransferase were designed and synthesized. All compounds were characterized by IR, MS and 1H NMR. The IC50 value of the target compounds against human Hela cells was evaluated and the result showed that all compounds exhibited antitumor activity, furthermore, the IC50 value of eleven compounds was smaller than that of 5-Fu. The tested activities of the target compounds were fit to those estimated using the hypothesis that was built by Catalyst, and the excellent correlation was got.

Key words: piperidone inhibitor of farnesyltransferase, computer-aided drug design, hypothesis, structure-activity relationship, antitumor activity