作者: Xiao-Meng Wang , Jing Xu , Min-Hang Xin , She-Min Lu , San-Qi Zhang
DOI: 10.1016/J.BMCL.2015.02.067
关键词:
摘要: Abstract In the present study, a series of m -(4-morpholino-1,3,5-triazin-2-yl)benzamides were designed, synthesized and characterized. Their antiproliferative activities against HCT-116 cell MCF-7 at 10 μM evaluated by MTT assay. Compounds T6 , T10 T11 T12 T19 exhibited potent activities. Thus, their IC 50 values cell, Hela U-87 MG A549 measured. The SAR target compounds was preliminary discussed. Western bolt assay suggested that compound can block PI3K/Akt/mTOR pathway. Hoechst staining indicated cause morphological changes induce apoptosis cells. These findings directly identify -(4-morpholinyl-1,3,5-triazin-2-yl)benzamide derivatives as novel agents further verify value benzamide fragment in drug design.