An amide of oleic acid and agonist of CB1 receptors (Ki = 8.13 μM); selective for CB1 over CB2 receptors, where it inhibits binding of the CB receptor full agonist CP55,940 by only 42.5% in HEK-293T cells expressing human CB2 receptors at 100 μM; inhibits forskolin-induced cAMP accumulation in N1E 115 mouse neuroblastoma cells; induces physiological sleep in rats at 5-50 mg; increases food intake in rats and anxiolytic-like effects in group-housed and socially isolated mice; induces transactivation of PPARα, PPARβ, and PPARγ; inhibits SERCA