Arylpiperazide derivatives of phenylpiperazines as a new class of potent and selective 5-HT1B receptor antagonists

被引:4
|
作者
Jorand-Lebrun, C [1 ]
Pauwels, PJ [1 ]
Palmier, C [1 ]
Chopin, P [1 ]
Moret, C [1 ]
Marien, M [1 ]
Halazy, S [1 ]
机构
[1] Ctr Rech Pierre Fabre, Dept Mol & Cellular Biol, F-81106 Castres, France
关键词
D O I
10.1016/S0960-894X(97)10164-0
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A new series of arylpiperazide derivatives of phenylpiperazines of general formula 4 has been prepared and evaluated as 5-HT1B receptor antagonists. In vitro experiments at human cloned 5-HT1B receptors show that these derivatives are potent and selective 5-HT1B receptor, antagonists. Among them, compound 4f was found to be orally active, to gain access to the CNS and more importantly to induce an increase in extracellular brain 5-HT upon systemic administration. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:3183 / 3188
页数:6
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