Purity >98% by HPLC. Endogenous anandamide-like compound. No affinity for CB1 receptors (Ki > 10 μM), VR1 receptors (EC50 > 10 μM) and anandamide transporters (IC50 > 50 μM). Displays hot-plate analgesia in mice and suppresses tonic inflammatory pain. A potent inhibitor of the Fatty Acid Amide Hydrolase (FAAH). Also reported to be a novel insulin secretagogues, increases [Ca2+]i through stimulation of the voltage-dependent Ca2+ channels.