N,N-disubstituted 4-amino-(6-methoxy)-3-phenyl-2H-naphtho [1,2-b]pyran-2-ones with antiarrhythmic, platelet antiaggregating and local anesthetic activities.

Il Farmaco; edizione scientifica Pub Date : 1988-11-01
A Bargagna, M Longobardi, E Mariani, P Schenone, S Russo, S Vilagliano, V De Novellis, E Marmo
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引用次数: 0

Abstract

The synthesis of title compounds (VI) by 1,4-cycloaddition of phenylchloroketene to N,N-disubstituted (E)-2-aminomethylene-3,4-dihydro-(6-methoxy)-1(2H)naphthalenones, followed by dehydrochlorination with DBN and dehydrogenation with Pd/C of the resulting cycloadducts, is described. Some compounds (VI) showed antiarrhythmic activity in rats higher or like that of quinidine and platelet antiaggregating activity in vitro like that of acetylsalycilic acid, as well as moderate infiltration anesthesia in mice and weak hypotensive, bradicardic and antiinflammatory activities in rats.

具有抗心律失常、抗血小板聚集和局部麻醉活性的N,N-二取代4-氨基-(6-甲氧基)-3-苯基- 2h -萘[1,2-b]吡喃-2- 1。
用1,4-苯基氯烯酮与N,N-二取代(E)-2-氨基甲基-3,4-二氢-(6-甲氧基)-1(2H)萘酮加成,然后用DBN脱氢氯化,再用Pd/C脱氢,合成了标题化合物(VI)。部分化合物(VI)在大鼠体内的抗心律失常活性高于或接近奎尼丁,体外抗血小板聚集活性类似于乙酰水杨酸,在小鼠体内具有中度浸润麻醉作用,在大鼠体内具有较弱的降压、心动缓和抗炎作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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