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寻找新型抗心律失常和降压化合物。新型1-[(2-羟基-3-氨基)]-丙基吡咯烷-2-酮衍生物的合成、抗心律失常、降压及α-肾上腺素能受体阻断活性

Search for new antiarrhythmic and hypotensive compounds. Synthesis, antiarrhythmic, antihypertensive, and alpha-adrenoceptor blocking activity of novel 1-[(2-hydroxy-3-amino)]-propylpyrrolidin-2-one derivatives.

作者信息

Filipek B, Sapa J, Malawska B, Kulig K, Antkiewicz-Michaluk L

机构信息

Laboratory of Pharmacological Screening, Collegium Medicum Jagiellonian University, Krakow, Poland.

出版信息

Arch Pharm (Weinheim). 1997 Jul;330(7):225-31. doi: 10.1002/ardp.19973300707.

Abstract

A series of the derivatives of 1-[2-hydroxy-3-(4-phenyl-1-piperazinyl])propyl]-pyrrolidin-2- one (MG-1) was synthesized and tested for electrocardiographic, antiarrhythmic, and antihypertensive activity as well as for alpha 1- and alpha 2-adrenoceptors binding affinities. Some of the compounds of this series slightly decreased the heart rate, prolonged P-Q, Q-T intervals and QRS complex. Only compound 7 (1-[2-hydroxy-3-(4-phenyl-1-piperazinyl)propyl]-pyrrolidine) possesses potent antiarrhythmic and a slight hypotensive properties, and affinity for alpha 1- and alpha 2-adrenoceptor. The results suggest that the antiarrhythmic and hypotensive effect of compound 7 and MG-1 is related to their adrenolytic properties, and that those properties depend on the presence of a phenylpiperazine moiety.

摘要

合成了一系列1-[2-羟基-3-(4-苯基-1-哌嗪基)丙基]-吡咯烷-2-酮(MG-1)的衍生物,并对其进行了心电图、抗心律失常、抗高血压活性以及α1和α2肾上腺素能受体结合亲和力的测试。该系列中的一些化合物略微降低了心率,延长了P-Q、Q-T间期和QRS波群。只有化合物7(1-[2-羟基-3-(4-苯基-1-哌嗪基)丙基]-吡咯烷)具有强效抗心律失常和轻微的降压特性,以及对α1和α2肾上腺素能受体的亲和力。结果表明,化合物7和MG-1的抗心律失常和降压作用与其抗肾上腺素特性有关,且这些特性取决于苯哌嗪部分的存在。

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