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螺琥珀酰亚胺作为潜在的抗惊厥药。

Spirosuccinimides as potential anticonvulsants.

作者信息

Tarver M L, Nicholson J M, Scott K R

出版信息

J Pharm Sci. 1985 Jul;74(7):785-7. doi: 10.1002/jps.2600740721.

Abstract

A series of spirosuccinimides was synthesized and evaluated for anticonvulsant activity. The study was designed to apply the Topliss approach to structure-activity correlations in this novel series of 2-substituted-2-azaspiro[4.4]nonane-1,3-diones and 2,4-disubstituted-2-azaspiro[4.4]nonane-1,3-diones. While no correlation was noted with the 2-substituted derivatives, a good correlation was obtained in the 2,4-disubstituted series, indicating that anticonvulsant activity was related to increasing tau values. The results of these anticonvulsant tests are presented and a rational approach to the structure-activity relationships of spirosuccinimides is provided.

摘要

合成了一系列螺琥珀酰亚胺,并对其抗惊厥活性进行了评估。该研究旨在将托普利斯方法应用于这一系列新型的2-取代-2-氮杂螺[4.4]壬烷-1,3-二酮和2,4-二取代-2-氮杂螺[4.4]壬烷-1,3-二酮的构效关系研究。虽然在2-取代衍生物中未发现相关性,但在2,4-二取代系列中获得了良好的相关性,表明抗惊厥活性与τ值的增加有关。本文展示了这些抗惊厥试验的结果,并提供了一种关于螺琥珀酰亚胺构效关系的合理方法。

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