Department of Organic Chemistry, Faculty of Science, Palacký University, 17 Listopadu 12, Olomouc 771 46, Czech Republic.
Carbohydr Res. 2011 Oct 18;346(14):2136-44. doi: 10.1016/j.carres.2011.07.026. Epub 2011 Aug 5.
A number of 5-alkoxymethyluracil analogues were synthesized to evaluate their cytotoxic activity. 5-Alkoxymethyluracil derivatives 1 were prepared via known nucleophilic substitution of 5-chloromethyluracil 5 and subsequently transformed to their corresponding nucleosides 2. All prepared compounds were submitted to cytotoxic activity testing against drug sensitive and drug resistant leukaemia cells and solid tumour derived cell lines. In addition, the cytotoxic activity of 5-alkoxymethyluracil analogues 1 and 2 was compared with the previously published 5-[alkoxy(4-nitrophenyl)methyl]uracil analogues 3 and 4. Extensive structure-cytotoxic activity relationship studies are reported.
合成了一系列 5-烷氧甲基尿嘧啶类似物,以评估其细胞毒性活性。5-烷氧甲基尿嘧啶衍生物 1 通过 5-氯甲基尿嘧啶 5 的已知亲核取代反应制备,随后转化为其相应的核苷 2。所有制备的化合物均进行了细胞毒性活性测试,针对药物敏感和耐药白血病细胞以及实体瘤衍生细胞系。此外,还将 5-烷氧甲基尿嘧啶类似物 1 和 2 的细胞毒性活性与先前报道的 5-[烷氧基(4-硝基苯基)甲基]尿嘧啶类似物 3 和 4 进行了比较。报告了广泛的结构-细胞毒性活性关系研究。