Novel Quinolizidinyl Derivatives as Antiarrhythmic Agents: 2. Further Investigation

被引：15

作者：

Tasso, Bruno ^{[1
]}

Budriesi, Roberta ^{[2
]}

Vazzana, Iana ^{[1
]}

Ioan, Pierfranco ^{[2
]}

Micucci, Matteo ^{[2
]}

Novelli, Federica ^{[1
]}

Tonelli, Michele ^{[1
]}

Sparatore, Anna ^{[3
]}

Chiarini, Alberto ^{[2
]}

Sparatore, Fabio ^{[1
]}

机构：

[1] Univ Genoa, Dipartimento Sci Farmaceut, I-16132 Genoa, Italy

[2] Univ Bologna, Dipartimento Sci Farmaceut, I-40126 Bologna, Italy

[3] Univ Milan, Dipartimento Sci Farmaceut, I-20133 Milan, Italy

来源：

JOURNAL OF MEDICINAL CHEMISTRY | 2010年 / 53卷 / 12期

关键词：

PHARMACOLOGICAL INTEREST; ATRIAL-FIBRILLATION; RECEPTOR ANTAGONISTS; 1-LUPINYLQUINOXALIN-2(1H)-ONES; METOCLOPRAMIDE; ARRHYTHMIAS; LUPININE; LIGANDS; DRUGS; 5-HT3;

D O I：

10.1021/jm100298d

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

Fifteen quinolizidine derivatives have been tested for antiarrhythmic, inotropic, and chronotropic effects on isolated guinea pig (gp) heart tissues and to assess calcium antagonist activity. All compounds exhibited from moderate to high antiarrhythmic activity, and five of them (3, 4, 6, 13, and 15) were more active and potent than the reference drugs (amiodarone, lidocaine, procainamide, and quinidine). These compounds were studied on spontaneously beating Langendorff-perfuse gp heart; even at concentration 17-67 times higher than the Corresponding EC50 for antiarrhythmic activity, they prolonged the QT intervals only moderately, comparing favorably with amiodarone and quinidine. Compounds 3 and 15 deserve further investigation due to their interesting cardiovascular profiles.

引用

页码：4668 / 4677

页数：10

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