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New antiarrhythmic agents. N-Aryl-8-pyrrolizidinealkanamides
Journal of Medicinal Chemistry1985Vol. 28(6), pp. 714–717
Citations Over TimeTop 10% of 1985 papers
S. MIYANO, Kunihiro Sumoto, Fumio Satoh, Keiyu Shima, Mariko Hayashimatsu, Minoru Morita, Kazuo Aisaka, Teruhisa Noguchi
Abstract
The synthesis and antiarrhythmic activity of N-aryl-8-pyrrolizidinealkanamides are described. The target compounds were evaluated for their ability to protect against chloroform-induced fibrillation in mice. Many of them were found to have antifibrillatory activity comparable to that of lidocaine; several are more potent than lidocaine. N-(2,6-Dimethylphenyl)-8-pyrrolizidineacetamide which was found to be more potent and less toxic (LD50) than lidocaine, also showed a long duration of action in dogs with ventricular arrhythmias after oral administration.
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