New 4-(4-methyl-phenyl)phthalazin-1(2H)-one derivatives and their effects on α1-receptors

被引:22
|
作者
Strappaghetti, G
Brodi, C
Giannaccini, G
Betti, L
机构
[1] Univ Perugia, Dipartimento Chim & Tecnol Farmaco, I-06123 Perugia, Italy
[2] Univ Pisa, Dipartimento Psichiatria Neurobiol Farmacol & Bio, I-56126 Pisa, Italy
关键词
alpha(1)-adrenoceptor affinity; alpha(2)-adrenoceptor affinity; 5HT(1A)-serotoninergic affinity; phenyl-phthalazinone fragment; arylpiperazines; structure-activity relationships (SAR);
D O I
10.1016/j.bmcl.2006.02.068
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Continuing our research aimed at obtaining new Compounds with high affinity and selectivity toward alpha(1)-AR, a new series of arylpiperazine derivatives was designed, synthesized, and biologically tested. The new Compounds 1-17 are characterized by a phenylphthalazin-1(2H)-one fragment connected through an alkyl chain to an arylpiperazine residue. The pharmacological profile of these compounds was evaluated for their affinity and selectivity toward alpha(1)-AR, alpha(2)-AR and toward 5HT(1A) serotoninergic receptor. A discussion on the structure-activity relationship (SAR) of these compounds is also reported. (C) 2006 Published by Elsevier Ltd.
引用
收藏
页码:2575 / 2579
页数:5
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