The evaluation of a series of piperazinyl carbamates and ureas, designed on the basis of previously reported TRPV1 antagonists and FAAH inhibitors, led to the identification of some 'dual-action' compounds targeting both FAAH and TRPV1 or TRPA1 receptors. (C) 2009 Elsevier Ltd. All rights reserved.

Synthesis and biological evaluation of piperazinyl carbamates and ureas as fatty acid amide hydrolase (FAAH) and transient receptor potential (TRP) channel dual ligands

De Petrocellis L;Ligresti A;Di Marzo V;
2009

Abstract

The evaluation of a series of piperazinyl carbamates and ureas, designed on the basis of previously reported TRPV1 antagonists and FAAH inhibitors, led to the identification of some 'dual-action' compounds targeting both FAAH and TRPV1 or TRPA1 receptors. (C) 2009 Elsevier Ltd. All rights reserved.
2009
Istituto di Chimica Biomolecolare - ICB - Sede Pozzuoli
Istituto di Scienze Applicate e Sistemi Intelligenti "Eduardo Caianiello" - ISASI
ENDOCANNABINOID SYSTEM
INHIBITORS
PAIN
PHARMACOLOGY
ANTAGONIST
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/144526
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