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III类抗心律失常药司美利特的芳基取代衍生物的合成及其心脏电生理活性。潜在的I/III类药物。

Synthesis and cardiac electrophysiological activity of aryl-substituted derivatives of the class III antiarrhythmic agent sematilide. Potential class I/III agents.

作者信息

Phillips G B, Morgan T K, Nickisch K, Lind J M, Gomez R P, Wohl R A, Argentieri T M, Sullivan M E

机构信息

Department of Medicinal Chemistry, Berlex Laboratories, Inc., Cedar Knolls, New Jersey 07927.

出版信息

J Med Chem. 1990 Feb;33(2):627-33. doi: 10.1021/jm00164a025.

Abstract

Twelve novel derivatives of the selective class III antiarrhythmic agent sematilide were prepared in an attempt to incorporate both class I and class III electrophysiological properties into a single molecule. Electrophysiological activity was determined by standard microelectrode techniques in canine cardiac Purkinje fibers. Initial assessment of class I efficacy was carried out in a ouabain-induced arrhythmia model in guinea pigs. All of the compounds prolonged action potential duration in Purkinje fibers (class III activity), and three were active against ouabain-induced arrhythmias (class I activity). Selected compounds were evaluated further in dogs for efficacy against arrhythmias occurring 24 h following coronary ligation (automatic arrhythmias) and induced by using programmed electrical stimulation techniques (reentrant arrhythmias). The most effective compounds from the series are 3g and -j, which were effective in both canine models. Molecular modeling and structure-activity relationships are discussed.

摘要

制备了12种新型的选择性III类抗心律失常药物司美利特衍生物,试图将I类和III类电生理特性整合到一个分子中。通过标准微电极技术在犬心脏浦肯野纤维中测定电生理活性。在哇巴因诱导的豚鼠心律失常模型中对I类疗效进行了初步评估。所有化合物均延长了浦肯野纤维的动作电位时程(III类活性),其中三种对哇巴因诱导的心律失常有活性(I类活性)。对选定的化合物在犬中进一步评估其对冠状动脉结扎后24小时发生的心律失常(自律性心律失常)和使用程控电刺激技术诱发的心律失常(折返性心律失常)的疗效。该系列中最有效的化合物是3g和3j,它们在两种犬模型中均有效。讨论了分子建模和构效关系。

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