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苯琥胺某些新衍生物的抗惊厥特性

Anticonvulsant properties of some new derivatives of phensuccinimide.

作者信息

Rump S, Ilczuk I, Walczyna K

出版信息

Arzneimittelforschung. 1979;29(2):290-2.

PMID:582142
Abstract

Anticonvulsant properties of two new derivatives, of phenylsuccinimide, N-morpholinomethyl-3-bromophenyl-succinimide(IL-7) and N-amino-3-bromophenylsuccinimide (IL-16), were studied. It was stated that both compounds have similar acute toxicity and act longer than phensuximide. They are especially active in maximal electroshock seizure (MES) test. Their effectiveness against convulsions produced by pentetrazole is less than that of phensuximide. Their effectiveness against procaine and strychnine is similar, only one of tested compounds has very high potency against strychnine. This compound, IL-16, has also a different pattern of effect-time which is probably due to its different pharmacokinetic behaviour.

摘要

研究了两种新的苯基琥珀酰亚胺衍生物,N-吗啉甲基-3-溴苯基琥珀酰亚胺(IL-7)和N-氨基-3-溴苯基琥珀酰亚胺(IL-16)的抗惊厥特性。据称,这两种化合物具有相似的急性毒性,且作用时间比苯琥胺长。它们在最大电休克惊厥(MES)试验中特别有效。它们对戊四氮引起的惊厥的有效性低于苯琥胺。它们对普鲁卡因和士的宁的有效性相似,只有一种受试化合物对士的宁具有非常高的效力。这种化合物,IL-16,也有不同的效应时间模式,这可能是由于其不同的药代动力学行为。

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