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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 dipyro...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9781268/ https://www.ncbi.nlm.nih.gov/pubmed/36558970 http://dx.doi.org/10.3390/ph15121519 |
Sumario: | 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. |
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