有机化学 ›› 2011, Vol. 31 ›› Issue (08): 1266-1271. 上一篇    下一篇

研究简报

含嘧啶氨基的三取代三嗪衍生物的合成及其抗菌、抗肿瘤活性研究

陈华*,1,谷云景1,苑香果1,赵莲1,赵建鹏1,秦占斌1,刘丽2,李小六*,1,曹克强2,张金超1   

  1. (1河北大学化学与环境科学学院 河北省化学生物学重点实验室 保定 071002)
    (2河北农业大学植物保护学院 保定 071001)
  • 收稿日期:2011-01-11 修回日期:2011-03-12 发布日期:2011-03-12
  • 通讯作者: 陈华 E-mail:hua-todd@163.com

Synthesis and Antifungal, Anti-tumor Studies of the Trisubstitued Triazines Bearing Aminopyrimidine Group

Chen Hua*,1 Gu Yunjing1 Yuan Xiang-guo1 Zhao Lian1 Zhao Jianpeng1 Qin Zhanbin1 Liu Li2 Li Xiaoliu*,1 Cao Keqiang2 Zhang Jinchao1   

  1. (1 Key Laboratory of Chemical Biology of Hebei Province, College of Chemistry and Environmental Science, Hebei University, Baoding 071002)
    (2 College of Plant Protec-tion, Hebei Agricultural University, Baoding 071001)
  • Received:2011-01-11 Revised:2011-03-12 Published:2011-03-12

以三聚氯氰为起始原料, 合成了系列新的含嘧啶氨基的2,4,6-三取代-1,3,5-三嗪化合物, 并测试了化合物抗苹果树腐烂病菌和抑制肿瘤细胞增殖活性. 结果表明, 化合物2aa2cb3aa3cb对苹果树腐烂病菌具有显著的抑制作用, 具有开发为新型植物抗菌剂的潜力. 部分化合物, 如4ba4ca分别对胃癌(BGC-823)和宫颈癌(Hela)肿瘤细胞具有较强的抑制活性, IC50分别为10.9和11.3 μmol/L.

关键词: 嘧啶氨基, 三嗪化合物, 抗菌活性, 抗肿瘤活性

A series of novel trisubstituted 1,3,5-triazine compounds bearing aminopyrimidine group were synthesized using cyanuric chloride as the starting material. The antifungal activitiy against Valsa mali and antiproliferative activity for three tumor cells of all the triazine compounds were evaluated. The results showed that a majority of the compounds 2aa2cb and 3aa3cb have notable inhibitory activity against Valsa mali. Some compounds, such as 4ba and 4ca, showed good cytotoxicity to BGC-823 and Hela tumor cells with the IC50 value of 10.9 and 11.3 μmol/L, respectively, higher than that of the positive control cisplatin.

Key words: aminopyrimidine, triazine, antifungal activity, anti-tumor activity