Author/Authors :
F. Minutolo، نويسنده , , M.G. Cascio، نويسنده , , I. Carboni، نويسنده , , T. Bisogno، نويسنده , , G. Prota، نويسنده , , S. Bertini، نويسنده , , Paul M. DiGiacomo، نويسنده , , M. Bifulco، نويسنده , , V. Di Marzo، نويسنده , , M. Macchia، نويسنده ,
Abstract :
Biphenylic ester derivatives, designed by using a ‘soft-drug’ approach, proved to possess good binding properties toward cannabinoid CB1 and CB2 receptors and, at the same time, their metabolically labile ester portion would promote a rapid systemic inactivation. This may constitute a possible solution to the psychotropic side effects encountered when cannabinoids are therapeutically employed as local analgesic or antiglaucoma agents.
Keywords :
CB2 , Retrometabolic , Soft-drugs , CB1 , Cannabinoids