5-dialkylaminomethylhydantoins against Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) strains, some molecular modifications were attempted. The antibacterial activities of all of the synthesized hydantoin derivatives were evaluated. Among the hydantoin derivatives designed in this study, C₂-symmetrical twin-drug type compound (7) showed the highest level of antibacterial activity
与我们对5-二烷基
氨基甲基乙内酰
脲类抗革兰氏阴性(大肠埃希氏菌)和革兰氏阳性(
金黄色葡萄球菌)菌株的抗菌化合物的研究有关,尝试了一些分子修饰。评价了所有合成的乙内酰
脲衍
生物的抗菌活性。在这项研究设计的乙内酰
脲衍
生物中,C 2-对称双药型化合物(7)对
金黄色葡萄球菌菌株显示出最高
水平的抗菌活性。