Hagen V, Rumler A, Klauschenz E, Hagen A, Heer S, Faust G, Mitzner R
Akademie der Wissenschaften, DDR.
Pharmazie. 1990 Apr;45(4):240-1.
The title compounds were synthesized by treating of 2-chloro-pyridines 1-3 with the appropriate aminoalkylamines or piperazines. In isolated guinea pig atria some compounds showed greater positive inotropic activity than amrinone. Heart rate was decreased or remained unchanged. In anesthetized dogs some derivatives exerted a dose-dependent increase in myocardial contractility and, additionally, a decrease in blood pressure.
通过用适当的氨基烷基胺或哌嗪处理2-氯吡啶1-3合成了标题化合物。在分离的豚鼠心房中,一些化合物显示出比氨力农更强的正性肌力活性。心率降低或保持不变。在麻醉犬中,一些衍生物使心肌收缩力呈剂量依赖性增加,此外,血压降低。