Synthesis, computational and biological activity of heteroatomic compounds based on phenylthiourea and acetophenone
作者:Vagif Farzaliyev、Aleksey Shuriberko、Afsun Sujayev、Sabiya Osmanova、Sevinj Gojayeva、Konul Gahramanova
DOI:10.1016/j.molstruc.2020.128844
日期:2020.12
structure analysis. As a result of studies, it was found that the greatest biological activity that can be useful in creating drugs is compound 1-(6-Methyl-3-phenyl-2-sulfanylidene-1,2,3,4-tetrahydropyrimidin-5-yl)ethanone. This compound is characterized by antioxidant effect significant effect on the functioning of biological membranes, and in low concentrations (below 7.5 mg/l) it stabilizes the membranes
摘要 本文致力于有机化学的一个有前途的方向——合成具有生理特性的新型含硫和氮的硫脲和苯乙酮衍生物。因此首次以苯硫脲、乙酰丙酮和37%甲醛(福尔马林)水溶液在三氟乙酸存在下合成1-(6-Methyl-3-phenyl-2-sulfanylidene- 1,2,3,4-四氢嘧啶-5-基)乙酮。此外,根据苯乙酮及其一些对位取代衍生物的硫酰化反应,我们合成了2,2'-((1-苯基乙烷-1,1-二基)双(硫烷二基))二乙酸。进行合成 2,2'-((1-苯基乙烷-1,1-二基)双(硫烷二基))二乙酸与伯胺的直接酰胺化反应。新化合物的结构通过核磁共振谱和 X 射线结构分析进行解释。研究结果发现,可用于制造药物的最大生物活性是化合物 1-(6-Methyl-3-phenyl-2-sulfanylidene-1,2,3,4-tetrahydropyrimidin-5-基)乙酮。这种化合物的特点是抗氧化作用对生物膜的功能有显着影响,在低浓度(低于