Synthesis, Molecular Docking, and Hemorheological Activity of New 4-(Thien-2-yl)-3-aminopyridine-2(1H)-one Derivatives
作者:I. V. Palamarchuk、Z. T. Shulgau、Sh. D. Sergazy、A. M. Zhulikeeva、T. M. Seilkhanov、I. V. Kulakov
DOI:10.1134/s1070363222090110
日期:2022.9
the basis of 4-(thien-2-yl)-3-aminopyridine-2(1H)-one, the corresponding chloroacetamide and condensed 1H-pyrido[2,3-b][1,4]oxazine-2(3H)-one were synthesized by the reaction of acylation with chloroacetyl chloride. Thioureide derivatives of 3-aminopyridine-2(1H)-one were obtained by reactions with a number of isothiocyanates. It was shown that the carbamothionylmethacrylamide derivative cyclizes rather
摘要 以4-(thien-2-yl)-3-aminopyridine-2(1 H )-one为基础,得到相应的氯乙酰胺和缩合的1 H- pyrido[2,3 -b ][1,4]oxazine-2 (3H)-one是通过与氯乙酰氯的酰化反应合成的。3-氨基吡啶-2(1 H )的硫脲衍生物)-一种是通过与许多异硫氰酸酯反应获得的。结果表明氨基甲硫基甲基丙烯酰胺衍生物相当容易环化成取代的1,3-噻嗪。进行了用于抗血栓活性的合成衍生物的分子对接,这表明吡啶酮核心中硫脲片段的存在导致对所选蛋白质的亲和力增加。使用增加的血液粘度综合征的体外模型对化合物的血液流变学研究也显示了在参考药物己酮可可碱水平上的活性。