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一些新型N-取代的α-芳基/烷基琥珀酰亚胺作为潜在的抗惊厥药。

Some new N-substituted alpha-aryl/alkyl succinimides as possible anticonvulsants.

作者信息

Amir M, Singh E

机构信息

Department of Medicinal Chemistry, Jamia Hamdard, Hamdard Nagar, New Delhi, India.

出版信息

Pharmazie. 1991 Oct;46(10):705-7.

PMID:1803384
Abstract

In view of their expected MAO inhibitory CNS depressant and anticonvulsant properties a number of N-(5-alkyl-1,3,4-thiadiazol-2-yl)-alpha-aryl/alkyl succinimides (1-20) and N-(cyclohexyl)-alpha-aryl/alkyl succinimides (21-25) have been synthesized. Some of them when screened for anticonvulsant activity against pentetrazole induced seizures in mice at a dose of 80 mg/kg were found to be 10 to 50% active.

摘要

鉴于其预期的单胺氧化酶抑制、中枢神经系统抑制和抗惊厥特性,已合成了多种N-(5-烷基-1,3,4-噻二唑-2-基)-α-芳基/烷基琥珀酰亚胺(1-20)和N-(环己基)-α-芳基/烷基琥珀酰亚胺(21-25)。其中一些化合物在以80mg/kg的剂量对小鼠进行戊四氮诱发惊厥的抗惊厥活性筛选时,发现其活性为10%至50%。

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