Synthesis and antitumor activity of novel 2-amino-4-(3,5,5-trimethyl-2-pyrazolino)-1,3,5-triazine derivatives

被引:56
作者
Brzozowski, Z [1 ]
Saczewski, F [1 ]
机构
[1] Med Univ Gkansk, Dept Chem Technol Drugs, PL-80416 Gdansk, Poland
关键词
2-amino-4-(3,5,5-trimethyl-2-pyrazolino)-1,3,5-triazine derivatives; synthesis; structures; antitumor effect;
D O I
10.1016/S0223-5234(02)01379-X
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The syntheses and antitumor activities of novel 2-amino-4-(3,5,5-trimethyl-2-pyrazolino)-1,3,5-triazine derivatives 4-38 are described. All the compounds prepared were screened at the National Cancer Institute (NCI) for their activities against a panel of 60 tumor cell lines and relationships between structure and antitumor activity in vitro are discussed. The triazines 11, 16, 20, 23, 23 and 34-38 exhibited modest or fairly high activity against one or more human tumor cell lines. Prominent compound with remarkable activity (log G150, < - 8.00- -5.00) to all investigated cell lines and highly potent (log G150. < - 8.00- -7.64) against some cell lines of Leukemia (CCRF-CEM, K-562, RPMI-8226, SR), CNS Cancer (SF-539) and Breast Cancer (T-47D) was 2-[2-amino-4-(3,5,5-trimethyl-2-pyrazolino)-1,3,5-triazin-6-yl]-3-(5-nitro-2-thienyl)acrylonitrile (25). (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
引用
收藏
页码:709 / 720
页数:12
相关论文
共 20 条
  • [1] BOYD M R, 1989, Proceedings of the American Association for Cancer Research Annual Meeting, V30, P652
  • [2] BRZOZOWSKI Z, 1979, ACTA POL PHARM, V36, P401
  • [3] Synthesis, structural characterization and antitumor activity of novel 2,4-diamino-1,3,5-triazine derivatives
    Brzozowski, Z
    Saczewski, F
    Gdaniec, M
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2000, 35 (12) : 1053 - 1064
  • [4] CZERNEY P, 1981, Z CHEM, V21, P408
  • [5] SYNTHESIS AND CYTOTOXIC EVALUATION OF SOME STYRYL KETONES AND RELATED-COMPOUNDS
    DIMMOCK, JR
    KUMAR, P
    QUAIL, JW
    PUGAZHENTHI, U
    YANG, J
    CHEN, M
    REID, RS
    ALLEN, TM
    KAO, GY
    COLE, SPC
    BATIST, G
    BALZARINI, J
    DECLERCQ, E
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1995, 30 (03) : 209 - 217
  • [6] DIMMOCK JR, 1983, EUR J MED CHEM, V18, P248
  • [7] Tyrphostins .5. Potent inhibitors of platelet-derived growth factor receptor tyrosine kinase: Structure-activity relationships in quinoxalines, quinolines, and indole tyrphostins
    Gazit, A
    App, H
    McMahon, G
    Chen, J
    Levitzki, A
    Bohmer, FD
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (11) : 2170 - 2177
  • [8] Tyrphostins .6. Dimeric benzylidenemalononitrile tyrphostins: Potent inhibitors of EGF receptor tyrosine kinase in vitro
    Gazit, A
    Osherov, N
    Gilon, C
    Levitzki, A
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (25) : 4905 - 4911
  • [9] HAMAN NW, 1978, J PHARM SCI, V67, P1539
  • [10] HAYOSHI S, 1969, CHEM PHARM BULL, V17, P329