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外消旋2-氨基-N-取代琥珀酰亚胺衍生物的合成与抗惊厥活性

Synthesis and anticonvulsant activity of racemic 2-amino-N-substituted succinimide derivatives.

作者信息

Crider A M, Kolczynski T M, Miskell D L

出版信息

J Pharm Sci. 1981 Feb;70(2):192-5. doi: 10.1002/jps.2600700220.

Abstract

Several derivatives of (R,S)-2-amino-N-substituted succinimides were synthetized and evaluated in mice against seizures produced by electroshock and pentylenetetrazol. The most active compound against both electroshock- and pentylenetetrazol-induced seizures was (R,S)-N-benzyl-2-(methanesulfamido)succinimide.

摘要

合成了几种(R,S)-2-氨基-N-取代琥珀酰亚胺的衍生物,并在小鼠中针对电休克和戊四氮引发的癫痫进行了评估。对电休克和戊四氮诱导的癫痫最具活性的化合物是(R,S)-N-苄基-2-(甲磺酰胺基)琥珀酰亚胺。

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