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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.
- 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.
- Subjects :
- Animals
Azepines pharmacokinetics
Azepines therapeutic use
Central Nervous System drug effects
Orexin Receptors
Rats
Receptors, G-Protein-Coupled metabolism
Receptors, Neuropeptide metabolism
Structure-Activity Relationship
Azepines chemistry
Receptors, G-Protein-Coupled antagonists & inhibitors
Receptors, Neuropeptide antagonists & inhibitors
Sleep Wake Disorders drug therapy
Subjects
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