芳基
吲哚试验
取代基
化学
抗焦虑药
药物化学
立体化学
有机化学
生物化学
烷基
受体
作者
Tiurenkov In,В. В. Багметова,Ivanova Ov,Berestovitskaia Vm,О. С. Васильева,Ostrogliadov Es
摘要
The anxiosedative properties of 2-hydroxyimino-3-indolylyl(aryl)-4-oxo-2,3,4,5,6,7-hexahydrobenzofuranon derivatives have been studied using the open-field test, elevated plus-maze test, and conflict drinking procedure as developed by Vogel. It is established that all derivatives with both indole and aryl substituents produce a sedative effect. However, an anxiolytic effect is determined by the presence of indole substituent in the third position of the hexahydrobenzofuran molecule.
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