2-Arylpropionic Acid Pyrazolamides as Cannabinoid CB2 Receptor Inverse Agonists Endowed with Anti-Inflammatory Properties.

Among the most recent proposals regarding the mechanism of action of dipyrone, the modulation of cannabinoid receptors CB 1 and CB 2 appears to be a promising hypothesis. In this context, the present work describes a series of five novel pyrazolamides ( 7 - 11 ) designed as molecular hybrids of dipyrone metabolites and NSAIDs, such as ibuprofen and flurbiprofen. Target compounds were obtained in good overall yields (50-80%) by classical amide coupling between 4-aminoantipyrine and arylacetic or arylpropionic acids, followed in some cases by N -methylation of the amide group. The compounds presented good physicochemical properties in addition to stability to chemical (pH 2 and 7.4) and enzymatic (plasma esterases) hydrolysis and showed medium to high gastrointestinal and BBB permeabilities in the PAMPA assay. When subjected to functional testing on CB 1 - or CB 2 -transfected cells, compounds demonstrated an inverse agonist profile on CB 2 receptors and the further characterization of compound LASSBio-2265 ( 11 ) revealed moderate binding affinity to CB 2 receptor (K i = 16 µM) with an EC 50 = 0.36 µM (E max = 63%). LASSBio-2265 ( 11 ) (at 1, 3, and 10 mg/kg p.o.) was investigated in the formalin test in mice and a remarkable analgesic activity in the late inflammatory phase was observed, suggesting it could be promising for the treatment of pain syndromes associated with chronic inflammatory diseases.