Fatty acid amide hydrolase inhibitors. Surprising selectivity of chiral azetidine ureas-Reference-Cited by-同舟云学术

Fatty acid amide hydrolase inhibitors. Surprising selectivity of chiral azetidine ureas

Published:2009-08 Issue:15 Volume:19 Page:4241-4244
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Hart Terance,Macias Alba T.,Benwell Karen,Brooks Teresa,D’Alessandro Jalanie,Dokurno Pawel,Francis Geraint,Gibbons Ben,Haymes Timothy,Kennett Guy,Lightowler Sean,Mansell Howard,Matassova Natalia,Misra Anil,Padfield Anthony,Parsons Rachel,Pratt Robert,Robertson Alan,Walls Steven,Wong Melanie,Roughley Stephen

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference16 articles.

1. Enzymatic Pathways That Regulate Endocannabinoid Signaling in the Nervous System

2. Mice lacking fatty acid amide hydrolase exhibit a cannabinoid receptor-mediated phenotypic hypoalgesia

3. Selective blockade of 2-arachidonoylglycerol hydrolysis produces cannabinoid behavioral effects

4. Discovery of a Potent, Selective, and Efficacious Class of Reversible α-Ketoheterocycle Inhibitors of Fatty Acid Amide Hydrolase Effective as Analgesics

5. Thiadiazolopiperazinyl ureas as inhibitors of fatty acid amide hydrolase

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