Carato P, Depreux P, Lesieur D, Millan M, Newman-Tancredi A, Rettori M C, Caignard D H
lnstitut de Chimie Pharmaceutique Charles Lespagnol, Lille.
Drug Des Discov. 2000;17(2):173-81.
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.
设计并研究了一系列新型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条原创的合成路线。发现一些受试化合物在D4受体上与氯氮平一样有效。此外,选择了显示出高D2/D4选择性比率(>122)的化合物进行进一步的药理学评估。