Synthesis, physicochemical and preliminary pharmacological properties of N-[beta-hydroxy-gamma-(N-phenylpiperazinepropyl)]-2-pyrrolidinone.

B Malawska, M Gorczyca, B Filipek
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引用次数: 0

Abstract

The present paper reports on the synthesis and preliminary pharmacological properties of N-[beta-hydroxy-gamma-(N-phenylpiperazinepropyl)]-2- pyrrolidinone (MG-1). MG-1 was obtained by aminolysis of 1-(beta, gamma-epoxypropyl)-2-pyrrolidinone and N-phenylpiperazine. Its structure was established by elemental and spectral analyses (IR, UV, MS, 1H, 13C, 2D H-H and 2D C-H NMR). The antiarrhythmic activity of MG-1 was investigated on mice, rats and guinea pigs, using several models of arrhythmia. MG-1 attenuated or prevented the adrenaline- and barium chloride-induced arrhythmia. MG-1 demonstrated potent local anesthetic properties and depressed the depolarization phase of the action potential of cardiac cells. These results indicate that MG-1 possesses antiarrhythmic activity.

N-[β -羟基- γ -(N-苯基哌嗪丙基)]-2-吡咯烷酮的合成、理化性质及初步药理学性质。
本文报道了N-[β -羟基- γ -(N-苯基哌嗪丙基)]-2-吡咯烷酮(MG-1)的合成及其初步药理性质。MG-1由1-(β, γ -环氧丙基)-2-吡咯烷酮和n -苯哌嗪氨解得到。通过元素分析和光谱分析(IR、UV、MS、1H、13C、2D H-H和2D C-H NMR)确定了其结构。采用多种心律失常模型,在小鼠、大鼠和豚鼠身上研究了MG-1的抗心律失常活性。MG-1可减轻或预防肾上腺素和氯化钡引起的心律失常。MG-1表现出强大的局部麻醉特性,并抑制心肌细胞动作电位的去极化期。这些结果表明MG-1具有抗心律失常活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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