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Discovery of a potent, CNS-penetrant orexin receptor antagonist based on an n,n-disubstituted-1,4-diazepane scaffold that promotes sleep in rats.

Authors :
Whitman DB
Cox CD
Breslin MJ
Brashear KM
Schreier JD
Bogusky MJ
Bednar RA
Lemaire W
Bruno JG
Hartman GD
Reiss DR
Harrell CM
Kraus RL
Li Y
Garson SL
Doran SM
Prueksaritanont T
Li C
Winrow CJ
Koblan KS
Renger JJ
Coleman PJ
Source :
ChemMedChem [ChemMedChem] 2009 Jul; Vol. 4 (7), pp. 1069-74.
Publication Year :
2009

Abstract

Silent Night: Antagonism of the orexin (or hypocretin) system has recently been identified as a novel mechanism for the treatment of insomnia. Herein, we describe discovery of a dual (OX(1)R/OX(2)R) orexin receptor antagonist featuring a 1,4-diazepane central constraint that blocks orexin signaling in vivo. In telemetry-implanted rats, oral administration of this antagonist produced a decrease in wakefulness, while increasing REM and non-REM sleep.

Details

Language :
English
ISSN :
1860-7187
Volume :
4
Issue :
7
Database :
MEDLINE
Journal :
ChemMedChem
Publication Type :
Academic Journal
Accession number :
19418500
Full Text :
https://doi.org/10.1002/cmdc.200900069