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.
Original language | English |
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Pages (from-to) | 4878-4881 |
Number of pages | 4 |
Journal | Bioorganic and Medicinal Chemistry Letters |
Volume | 17 |
Issue number | 17 |
Early online date | 20 Jun 2007 |
DOIs | |
Publication status | Published - 1 Sep 2007 |
Keywords
- Cannabinoids
- CB
- Retrometabolic
- Soft-drugs