Design, synthesis, and evaluation of novel boronic-chalcone derivatives as antitumor agents

被引:303
作者
Kumar, SK [1 ]
Hager, E [1 ]
Pettit, C [1 ]
Gurulingappa, H [1 ]
Davidson, NE [1 ]
Khan, SR [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Div Expt Therapeut, Baltimore, MD 21231 USA
关键词
D O I
10.1021/jm030213+
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of boronic-chalcone derivatives were synthesized and tested for antitumor activity against human breast cancer cell lines. The results show the boronic-chalcones are more toxic to breast cancer cells compared to normal breast cells than other known chalcones.
引用
收藏
页码:2813 / 2815
页数:3
相关论文
共 34 条
  • [31] p53 mediated death of cells overexpressing MDM2 by an inhibitor of MDM2 interaction with p53
    Wasylyk, C
    Salvi, R
    Argentini, M
    Dureuil, C
    Delumeau, I
    Abecassis, J
    Debussche, L
    Wasylyk, B
    [J]. ONCOGENE, 1999, 18 (11) : 1921 - 1934
  • [32] INHIBITION OF CARCINOGEN-INDUCED PULMONARY AND MAMMARY CARCINOGENESIS BY CHALCONE ADMINISTERED SUBSEQUENT TO CARCINOGEN EXPOSURE
    WATTENBERG, LW
    COCCIA, JB
    GALBRAITH, AR
    [J]. CANCER LETTERS, 1994, 83 (1-2) : 165 - 169
  • [33] THE POTENT ANTI-TUMOR-PROMOTING AGENT ISOLIQUIRITIGENIN
    YAMAMOTO, S
    AIZU, E
    JIANG, H
    NAKADATE, T
    KIYOTO, I
    WANG, JC
    KATO, R
    [J]. CARCINOGENESIS, 1991, 12 (02) : 317 - 323
  • [34] MDM2 oncogene as a novel target for human cancer therapy
    Zhang, RW
    Wang, H
    [J]. CURRENT PHARMACEUTICAL DESIGN, 2000, 6 (04) : 393 - 416