一系列新的芳基哌嗪基苯并唑-2- 1和苯并恶嗪-3- 1衍生物选择性D4配体的合成与结合研究。

Drug design and discovery Pub Date : 2000-01-01
P Carato, P Depreux, D Lesieur, M Millan, A Newman-Tancredi, M C Rettori, D H Caignard
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引用次数: 0

摘要

设计并研究了一系列新的芳基哌嗪甲基衍生物作为潜在的D4配体。这些化合物的合成需要一个原始的合成路线。一些被测试的化合物被发现在D4受体上与氯氮平一样有效。此外,选择D2/D4选择性比高(>122)的化合物进行进一步药理评价。
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 binding studies on a new series of arylpiperazino benzazol-2-one and benzoxazin-3-one derivatives as selective D4 ligands.

A series of new arylpiperazinomethyl derivatives was designed and studied as potential D4 ligands. The synthesis of these compounds required an original synthetic route. Some of the tested compounds were found to be as potent as clozapine at D4 receptors. Moreover, compounds which displayed a high D2/D4 selectivity ratio (>122) were selected for further pharmacological evaluation.

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