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[N-取代α-氨基羧酸的新型二环己基酰胺衍生物的抗心律失常活性]

[The anti-arrhythmia activity of new dicyclohexylamide derivatives of N-substituted alpha-aminocarboxylic acids].

作者信息

Berdiaev S U, Paliani-Katsitadze N Sh, Turilova A I, Kaverina N V, Likhosherstov A M, Lebedeva A S, Ogurtsov V A

机构信息

Institute of Pharmacology, Russian Academy of Medical Sciences, Moscow, Russia.

出版信息

Eksp Klin Farmakol. 1999 Jul-Aug;62(4):26-9.

Abstract

Experiments on arrhythmia models showed a high antiarrhythmic activity of new derivatives of dicyclohexylamides of N-replaced alpha-aminocarbonic acids. The new compounds surpassed in intensity and duration of the antiarrhythmic effect the standard agents with classes I and III antiarrhythmic activity. In doing so they raise myocardial electrical stability and prevent sudden development of ventricular fibrillation. According to the mechanism of the antiarrhythmic activity, the new compounds may be related to antiarrhythmic agents possessing the properties of classes I and III.

摘要

对心律失常模型的实验表明,N-取代α-氨基羧酸二环己基酰胺的新衍生物具有很高的抗心律失常活性。这些新化合物在抗心律失常作用的强度和持续时间方面超过了具有I类和III类抗心律失常活性的标准药物。在此过程中,它们提高了心肌电稳定性,防止心室颤动的突然发生。根据抗心律失常活性的机制,这些新化合物可能与具有I类和III类特性的抗心律失常药物有关。

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