Author/Authors :
J. Ignacio Andrés، نويسنده , , Jes?s Alc?zar، نويسنده , , José M. Alonso-Meijide، نويسنده , , Rosa M. Alvarez، نويسنده , , Margot H. Bakker، نويسنده , , Ilse Biesmans، نويسنده , , José M. Cid، نويسنده , , Ana I. De Lucas، نويسنده , , Wilhelmus Drinkenburg، نويسنده , , Javier Fernandez-Suarez، نويسنده , , Luis M. Font، نويسنده , , Laura Iturrino، نويسنده , , Xavier Langlois، نويسنده , , Ilse Lenaerts، نويسنده , , Sonia Mart?nez، نويسنده , , Anton A. Megens، نويسنده , , Joaqu?n Pastor، نويسنده , , Shirley Pullan، نويسنده , , Thomas Steckler، نويسنده ,
Abstract :
In previous articles we have described the discovery of a new series of tricyclic isoxazolines combining central serotonin (5-HT) reuptake inhibition with α2-adrenoceptor antagonistic activity. We report now on the synthesis, the in vitro binding potency and the primary in vivo activity of six enantiomers within this series, one of which was selected for further pharmacological evaluation and assigned as R226161. Some additional in vivo studies in rats are described with this compound, which proved to be centrally and orally active as a combined 5-HT reuptake inhibitor and α2-adrenoceptor antagonist.
Keywords :
?2-Adrenoceptor blockade , Isoxazolines , Serotonin uptake inhibition , Antidepressant