N-(3,5-二甲氧基-4-丙氧基苯基-乙基)氮吡啶的惊厥性质及安定和三唑仑对其的影响。

J Herink
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引用次数: 0

摘要

研究了新合成的氮吡啶化合物N-(3,5-二甲氧基-4-丙氧基苯基-乙基)-氮吡啶(FAZ-4)在大鼠体内的惊厥活性。与传统的惊厥药戊四唑相比,主要发作缺乏强直成分。FAZ-4的这种作用可能是由于前脑机制没有中脑参与。两种抗惊厥药物以不同的方式测试抑制癫痫发作,但三唑安定比相同剂量的地西泮具有更强的抗惊厥活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Convulsive properties of N-(3,5-dimethoxy-4-propoxyphenyl-ethyl) aziridine and their influencing by diazepam and triazolam.

Convulsive activity of N-(3,5-dimethoxy-4-propoxy-phenyl-ethyl)-aziridine (FAZ-4), a newly synthetized aziridine compound was studied in rats. There is a lack of tonic component of major paroxysm in comparison with the classical convulsive agent pentylenetetrazol. This effect of FAZ-4 is probably due to the forebrain mechanism without the midbrain involvement. Both anticonvulsants tested suppressed seizures in a different manner, however triazolam exerted stronger anticonvulsive activity than the same dose of diazepam did.

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