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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 被引量:4

Synthesis and Antifungal,Anti-tumor Studies of the Trisubstitued Triazines Bearing Aminopyrimidine Group
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摘要 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2aa~2cb及3aa~3cb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4ba和4ca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11.3μmol/L. 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 mall and antiproliferative activity for three tumor cells of all the triazine compounds were evaluated. The results showed that a majority of the compounds 2aa^2cb and 3aa^3cb have notable inhibitory activity against Valsa mall 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 ~tmol/L, respectively, higher than that of the positive control cis- platin.
出处 《有机化学》 SCIE CAS CSCD 北大核心 2011年第8期1266-1271,共6页 Chinese Journal of Organic Chemistry
基金 国家自然科学基金(No.20902016) 河北省科学技术研究与发展计划(No.09276418D-13)资助项目
关键词 嘧啶氨基 三嗪化合物 抗菌活性 抗肿瘤活性 aminopyrimidine triazine antifungal activity anti-tumor activity
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