2-{4-[3-(4-aryl/heteroaryl-1-piperazinyl)propoxy]phenyl}-2H-benzotriazolesand their N-oxides as ligands for serotonin and dopamine receptors

Citation
A. Sparatore et al., 2-{4-[3-(4-aryl/heteroaryl-1-piperazinyl)propoxy]phenyl}-2H-benzotriazolesand their N-oxides as ligands for serotonin and dopamine receptors, FARMACO, 54(6), 1999, pp. 402-410
Citations number
24
Categorie Soggetti
Pharmacology & Toxicology
Journal title
FARMACO
ISSN journal
0014827X → ACNP
Volume
54
Issue
6
Year of publication
1999
Pages
402 - 410
Database
ISI
SICI code
0014-827X(19990630)54:6<402:2>2.0.ZU;2-Y
Abstract
A small set of 2-{4-[3-(4-aryl/heteroaryl-piperazinyl)propoxy]phenyl}-2H-be nzotriazoles and corresponding N-oxides were prepared. The synthesized comp ounds were able to bind on some serotonin (5-HT1A, 5-HT2A) and dopamine (D- 2, D-3) receptors, while displaying poor or no affinity for 5-HT1B, 5-NT2C, 5-HT3, and 5-HT4 subtypes. The strong contribution of the N-oxide function for the binding on 5-HT1A, D-2 and D-3 receptors is noteworthy. For 2-{4-[ 3-[4-(2-methoxyphenyl)-1-piperazinyl]propoxy]phenyl}-2H-benzotriazol-1-oxid e (4b), the binding constants (K-i) were 11.9 (5-HT1A) and 10.5 nM (D-3). I n a general pharmacological screening, the 2-{4-[3-(4-phenyl-1-piperazinyl) propoxy]phenyl}-2H-benzotriazole (3a) exhibited only very weak activities, with the exception of protecting mice from cyanide-induced hypoxia. (C) 199 9 Elsevier Science S.A. All rights reserved.