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具有天然单萜结构的普萘洛尔类似物作为一种有效的抗心律失常药物。

Propranolol analog with the natural monoterpene structure as a potent antiarrhythmic drug.

作者信息

Librowski T, Filipek B, Czarnecki R, Beresewicz A, Karwatowska-Prokopczuk E

机构信息

Department of Pharmacodynamics, Collegium Medicum Jagiellonian University, Kraków, Poland.

出版信息

Acta Pol Pharm. 1998 May-Jun;55(3):243-7.

PMID:9735705
Abstract

Antiarrhythmic effects and intracellular electrophysiological properties of a new antiarrhythmic compound (-)trans-4-[2-hydroxy-3(N-isopropylamino)-propoxyimino]-cis-car ane (9) were studied in several models of arrhythmia and in isolated guinea-pig myocardial preparations. Compound 9 prevented the aconitine-induced arrhythmia, reversed the ouabin-induced arrhythmia depressed the maximum rate depolarization (Vmax), and shortened the action potential duration (ADP) and the effective refractory period (ERP). The data indicate that compound 9 is an effective antiarrhythmic presumably with a class 1 B mechanism of action.

摘要

在多种心律失常模型及离体豚鼠心肌标本中,研究了一种新型抗心律失常化合物(-)反式-4-[2-羟基-3(N-异丙基氨基)-丙氧基亚氨基]-顺式蒈烷(9)的抗心律失常作用及细胞内电生理特性。化合物9可预防乌头碱诱发的心律失常,逆转哇巴因诱发的心律失常,降低最大去极化速率(Vmax),缩短动作电位时程(ADP)及有效不应期(ERP)。数据表明化合物9是一种有效的抗心律失常药物,其作用机制可能为ⅠB类。

相似文献

1
Propranolol analog with the natural monoterpene structure as a potent antiarrhythmic drug.具有天然单萜结构的普萘洛尔类似物作为一种有效的抗心律失常药物。
Acta Pol Pharm. 1998 May-Jun;55(3):243-7.
2
Propranolol analogs containing natural monoterpene structures: synthesis and pharmacological properties.含天然单萜结构的普萘洛尔类似物:合成与药理性质
Pol J Pharmacol Pharm. 1992 Nov-Dec;44(6):575-93.
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Effect of monoterpene derivative KP-19 on the pressor activity of catecholamines in rats.单萜衍生物KP-19对大鼠儿茶酚胺升压活性的影响。
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引用本文的文献

1
New Progress in Understanding the Cellular Mechanisms of Anti-arrhythmic Drugs.抗心律失常药物细胞机制认识的新进展
Open Life Sci. 2018 Sep 22;13:335-339. doi: 10.1515/biol-2018-0041. eCollection 2018 Jan.