Synthesis, biological evaluation and molecular docking studies of some pyrimidine derivatives
作者:Ahmed M. Fargualy、Nargues S. Habib、Khadiga A. Ismail、Ahmed M.M. Hassan、Marwa T.M. Sarg
DOI:10.1016/j.ejmech.2013.05.028
日期:2013.8
Some novel pyrimidine-5-carbonitrile derivatives bearing various substituent have been synthesized. The structures of target compounds were confirmed by elemental analysis and spectral data. Some selected members of the newly synthesized compounds were investigated for their cytotoxic potency against certain human tumor cell lines. Five representative active anticancer compounds 6a, 6c, 6d, 17a and
已经合成了一些带有各种取代基的新颖的嘧啶-5-腈衍生物。通过元素分析和光谱数据确认了目标化合物的结构。研究了新合成化合物的某些选定成员对某些人类肿瘤细胞系的细胞毒性。使用MOE程序,对两种酶的3D结构,对五个代表性的活性抗癌化合物6a,6c,6d,17a和18a进行对接。胸苷酸合酶和二氢叶酸还原酶。测试了合成化合物对金黄色葡萄球菌,铜绿假单胞菌的抗菌活性。,志贺志贺菌和白色念珠菌。化合物2c,7a和9c显示了广谱抗菌活性。