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苯基琥珀酰亚胺新环衍生物的药理特性及其对动物脑中去甲肾上腺素、多巴胺、血清素、5-羟吲哚乙酸、γ-氨基丁酸浓度和单胺氧化酶活性的影响。

Pharmacological properties of new cyclic derivatives of phenylsuccinimide and their influence on noradrenaline, dopamine, serotonin, 5-hydroxyindoleacetic acid, gamma-aminobutyric acid concentrations and monoaminooxidase activity in animal brains.

作者信息

Chmielewska B

出版信息

Pharmazie. 1984 Apr;39(4):259-62.

PMID:6204346
Abstract

Three new cyclic derivatives of phenylsuccinimide (I-10, I-11 and IL-7) were subjected to preliminary pharmacological studies in animals. Minimal peripheral action and inhibitory influence on the CNS were noted (only IL-7) was found to stimulate CNS). Neurotoxic effects were similar to those of the classical succinimides . Anticonvulsant activity and behavioral effects of tested compounds are discussed in the light of their influence on neurotransmitters.

摘要

对三种新的苯基琥珀酰亚胺环状衍生物(I - 10、I - 11和IL - 7)进行了动物初步药理学研究。观察到其外周作用极小,对中枢神经系统有抑制作用(仅IL - 7被发现可刺激中枢神经系统)。神经毒性作用与经典琥珀酰亚胺类相似。根据受试化合物对神经递质的影响,讨论了它们的抗惊厥活性和行为效应。

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