elemental analyses. Compounds 2a (3.1 times), 2c (3.8 times), 2f (4.6 times), 2g (1.3 times) and 3 (3.2 times) had 1.3-4.6 times higher cytotoxic potency than the reference compound 5-FU against Huh7 cell line while all the compounds synthesized had shown lower activities against T47D cell line than 5-FU. In the light of these results, compounds 2a, 2c, 2f, 2g and 3 may serve as model compounds for further
合成了一些4-
哌啶醇衍
生物,并测试了它们对人肝癌(Huh7)和乳腺癌(T47D)细胞的细胞毒性。芳基部分更改为2a中的苯基,2b中的4-甲基苯基,2c中的4-
甲氧基苯基,2d中的4-
氯苯基,2e中的4-
氟苯基,2f中的4-
溴苯基,2g中的4-
硝基苯基和3中的2-
噻吩基除2a和2d外,本研究首次合成并报道了化合物。
化学结构通过(1)1 H NMR,(13)C NMR,IR,MS和元素分析确认。化合物2a(3.1倍),2c(3.8倍),2f(4.6倍),2g(1.3倍)和3(3.2倍)对Huh7
细胞系的毒性比参考化合物5-FU高1.3-4.6倍,而所有合成的化合物对T47D
细胞系的活性均低于5-FU。根据这些结果,化合物2a,2c,2f,