Heteroarylureas with spirocyclic diamine cores as inhibitors of fatty acid amide hydrolase.
Bioorg Med Chem Lett
; 24(3): 737-41, 2014 Feb 01.
Article
en En
| MEDLINE
| ID: mdl-24433863
A series of mechanism based heteroaryl urea fatty acid amide hydrolase (FAAH) inhibitors with spirocyclic diamine cores is described. A potent member of this class, (37), was found to inhibit FAAH centrally, elevate the brain levels of three fatty acid ethanolamides [FAAs: anandamide (AEA), oleoyl ethanolamide (OEA) and palmitoyl ethanolamide (PEA)], and was moderately efficacious in a rat model of neuropathic pain.
Palabras clave
Texto completo:
1
Bases de datos:
MEDLINE
Asunto principal:
Compuestos de Espiro
/
Azetidinas
/
Urea
/
Diaminas
/
Amidohidrolasas
/
Compuestos Heterocíclicos
Límite:
Animals
Idioma:
En
Revista:
Bioorg Med Chem Lett
Asunto de la revista:
BIOQUIMICA
/
QUIMICA
Año:
2014
Tipo del documento:
Article