Title of article :
Synthesis, pharmacological evaluation and electrochemical studies of novel 6-nitro-3,4-methylenedioxyphenyl-N-acylhydrazone derivatives: Discovery of LASSBio-881, a new ligand of cannabinoid receptors Original Research Article
Author/Authors :
Carolina D. Duarte، نويسنده , , Jorge L.M. Tributino، نويسنده , , Daniel I. Lacerda، نويسنده , , Marina V. Martins، نويسنده , , Magna S. Alexandre-Moreira، نويسنده , , Fernando Dutra، نويسنده , , Etelvino J.H Bechara، نويسنده , , Francine S. de Paula، نويسنده , , Marilia O.F. Goulart، نويسنده , , Juliano Ferreira، نويسنده , , Jo?o B. Calixto، نويسنده , , Marise P. Nunes، نويسنده , , Alvaro L. Bertho، نويسنده , , Ana Luisa P. Miranda، نويسنده , , Eliezer J. Barreiro، نويسنده , , Carlos A.M. Fraga، نويسنده ,
Abstract :
We describe herein the discovery of LASSBio-881 (3c) as a novel in vivo antinociceptive, anti-inflammatory, and in vitro antiproliferative and antioxidant compound, with a cannabinoid ligand profile. We observed that LASSBio-881 (3c) was able to bind to CB1 receptors (71% at 100 μM) and also to inhibit T-cell proliferation (66% at 10 μM) probably by binding to CB2 receptors, in a non-proapoptotic manner, different from anandamide (1). It was also demonstrated that LASSBio-881 (3c) had an important antioxidant profile toward free radicals (DPPH and hydroxyl), probably due to its particular redox behavior, which reflects the presence of both nitro and 3,5-di-tert-butyl-4-hydroxyphenyl sub-units, as demonstrated by cyclic voltammetry studies. In addition, we showed that these structural sub-units are essential for the observed pharmacological activity.
Keywords :
Antioxidant activities , N-Acylhydrazone derivatives , Cannabinoid , Analgesic , Anti-inflammatory