哌嗪衍生物的合成及其正性肌力作用的初步研究

STUDIES ON SYNTHESIS AND INOTROPIC ACTIVITY OF PIPERAZINE DERIVATIVES

合成了两个系列共8个哌嗪类衍生物，用红外、核磁、质谱及元素分析确证结构。经豚鼠离体心房正性肌力作用试验，所筛选的8个化合物中，有7个具有不同程度的活性。其中目标物Ⅱ与Ⅸ正性肌力作用均强于对照品氨力农及维司力农（vesnarinone），且（Ⅸ）与氨力农比较有显著性差异。

Two series of compounds, including eight piperazine derivatives were synthesized, their structures were identified by using IR.NMR.MS and elemental analysis.The experiments of piperazine derivatives on inotropic activity of isolated atricum of guinea pigs showed that seven of the selected eight compounds have a range of activity. The inotropic activity of target compounds(Ⅱ) and (Ⅸ) was stronger than that of the contrast compounds amirinone and vesnarinone, and there was great different effect between (Ⅸ) and Amirinone.