Synthesis and biological evaluation of novel endocannabinoid probes, metabolically stable analogs, and N-acylethanolamine-hydrolyzing acid amidase ihibitors
The design of novel selective ligands is important for the structural characterization of G-protein coupled receptors (GPCR). For this reason we have sought to study the interactions of selective cannabinergic ligands with the CB1 and CB2 cannabinoid receptors to obtain information on the pharmacoph...
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| Online Access: | http://hdl.handle.net/2047/d20002788 |