Fluoxetine and its two enantiomers as selective serotonin uptake inhibitors.

Acta pharmaceutica Nordica Pub Date : 1990-01-01
D T Wong, R W Fuller, D W Robertson
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引用次数: 0

Abstract

The biochemical and pharmacological profiles of R,S-fluoxetine and its R and S enantiomers have been compared and reviewed. Both enantiomers exhibit profiles analogous to R,S-fluoxetine as inhibitors of serotonin uptake in vitro and in vivo with about equal potencies or a eudismic ratio near unity.

氟西汀及其两个对映体作为选择性血清素摄取抑制剂。
对R,S-氟西汀及其R和S对映体的生化和药理学特性进行了比较和综述。这两种对映体在体外和体内表现出类似于R, s -氟西汀的5 -羟色胺摄取抑制剂的特征,其效价大致相等或具有接近统一的感染比。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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