Bioorganic & Medicinal Chemistry Letters 2002-01-21

Synthesis and structure-activity relationship of 2-(aminoalkyl)-2,3,3a,8-tetrahydrodibenzo[c,f]isoxazolo[2,3-a]azepine derivatives: a novel series of 5-HT(2A/2C) receptor antagonists. Part 1.

J Ignacio Andrés, Jesús Alcázar, José M Alonso, Adolfo Díaz, Javier Fernández, Pilar Gil, Laura Iturrino, Encarna Matesanz, Theo F Meert, Anton Megens, Victor K Sipido

Index: Bioorg. Med. Chem. Lett. 12(2) , 243-48, (2002)

Full Text: HTML

Abstract

The synthesis of a series of novel 2-(aminoalkyl)-2,3,3a,8-tetrahydrodibenzo[c,f]isoxazolo[2,3-a]azepine derivatives as well as their 5-HT(2A/2C) and H(1) receptor binding affinities are described. The in vivo activity as potential anxiolytics of the synthesised compounds was measured in a mCPP challenge test. One of the compounds, 2a, proved to be a potent 5-HT(2A/2C) receptor antagonist showing as well oral activity and therefore could be considered as a potential anxiolytic/antidepressant agent.


Related Compounds

Related Articles:

New bis (imino) pyridine-iron (II)-and cobalt (II)-based catalysts: synthesis, characterization and activity towards polymerization of ethylene. Abu-Surrah AS, et al.

[J. Organomet. Chem. 648(1) , 55-61, (2002)]

Stereoselective synthesis of (R)-(-)-mianserin. Pawlowska J, et al.

[Tetrahedron Asymmetry 14(21) , 3335-3342, (2003)]

More Articles...