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茚并咪唑啉酮及相关杂环化合物在小鼠体内的抗惊厥活性

Anticonvulsive activity of indenoimidazolidinones and related heterocyclic compounds in mice.

作者信息

Alexander G J, Chatterjie N

出版信息

Res Commun Chem Pathol Pharmacol. 1980 Jan;27(1):45-56.

PMID:7361004
Abstract

A series of substituted cyclic ureides and related compounds, one of them a thio analog, were synthesized by condensing ninhydrin with urea, thiourea, dimethylurea or other aromatic or bifunctional agents. When tested against seizures induced in mice by the chemoconvulsant Metrazol or against audiogenic seizures, four compounds decreased either the incidence or the severity of convulsive manifestations and protected from mortality in seizures. The effective compounds were not toxic at the administered level (150 mg/kg) and produced few observable sedative effects.

摘要

通过茚三酮与尿素、硫脲、二甲基脲或其他芳香族或双功能试剂缩合,合成了一系列取代的环状酰脲及其相关化合物,其中一种是硫代类似物。当针对化学惊厥剂戊四氮诱导的小鼠惊厥或听源性惊厥进行测试时,四种化合物降低了惊厥表现的发生率或严重程度,并防止了惊厥导致的死亡。有效化合物在所给药剂量(150mg/kg)下无毒,且几乎没有可观察到的镇静作用。

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