1-(n -甲基苯胺乙基)吲哚的合成及其镇痛活性。

Acta pharmaceutica Nordica Pub Date : 1991-01-01
A Andreani, M Rambaldi, A Locatelli, F Andreani, R Bossa, I Galatulas, M Ninci
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引用次数: 0

摘要

报道了两个系列1-(n -甲基苯胺乙基)吲哚的合成。第一种是吲哚-3-乙酸或其甲基lester的n -烷基化反应,第二种是在适当的醛上通过Witting反应制备的。用热板法和苯基对苯醌致小鼠扭体法测定化合物的镇痛活性。这些化合物在热板试验中均无显著活性。而n -甲基苯基苯胺乙基1-(n -甲基苯胺乙基)-3-吲哚乙酸酯(7)在苯基对苯醌诱导扭体实验中活性最高,说明7具有外周镇痛作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and analgesic activity of 1-(N-methylanilinoethyl)indoles.

The synthesis of two series of 1-(N-methylanilinoethyl)indoles is reported. The first arises from the N-alkylation of indole-3-acetic acid or its methylester, while the second was prepared by means of the Witting reaction on the appropriate aldehyde. The compounds were tested in mice (hot plate test and phenyl-p-benzoquinone induced writhing test) for their analgesic activity. None of the compounds was significantly active in the hot plate test. However, N-methylanilinoethyl 1-(N-methylanilinoethyl)-3-indolylacetate (7) was the most active one in the phenyl-p-benzoquinone induced writhing test, which indicates that 7 has a peripheral analgesic effect.

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