Department of Organic Chemistry, University of Zagreb, Zagreb, Croatia.
Molecules. 2012 Sep 12;17(9):11010-25. doi: 10.3390/molecules170911010.
We report here on the synthesis and in vitro anti-tumor effects of a series of novel 1,2,4-triazole (compounds 3-6), 4,5-dicyanoimidazole (compound 7), and purine (compounds 8-13) coumarin derivatives and their acyclic nucleoside analogues 14-18. Structures of novel compounds 3-18 were deduced from their (1)H- and (13)C-NMR and corresponding mass spectra. Results of anti-proliferative assays performed on a panel of selected human tumor cell lines revealed that compound 6 had moderate cytostatic activity against the HeLa cell line (IC(50) = 35 µM), whereas compound 10 showed moderate activity against the HeLa (IC(50) = 33 µM), HepG2 (IC(50) = 25 µM) and SW620 (IC(50) = 35 µM) cell lines. These compounds showed no cytotoxic effects on normal (diploid) human fibroblasts.
我们在此报告一系列新型 1,2,4-三唑(化合物 3-6)、4,5-二氰基咪唑(化合物 7)和嘌呤(化合物 8-13)香豆素衍生物及其无环核苷类似物 14-18 的合成及体外抗肿瘤作用。新型化合物 3-18 的结构是根据它们的 (1)H-NMR 和 (13)C-NMR 以及相应的质谱推导出来的。对一组选定的人类肿瘤细胞系进行的抗增殖活性测定结果表明,化合物 6 对 HeLa 细胞系具有中等的细胞生长抑制活性(IC(50) = 35 µM),而化合物 10 对 HeLa(IC(50) = 33 µM)、HepG2(IC(50) = 25 µM)和 SW620(IC(50) = 35 µM)细胞系具有中等活性。这些化合物对正常(二倍体)人成纤维细胞没有细胞毒性作用。