A 3-furyl arachidonoyl analog that acts as a potent and selective reuptake inhibitor of AEA (IC50 = 0.8 µM) but has low affinity for FAAH (IC50 = 30 µM) potentiates the biological effects of AEA when co-administered in rats.
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A 3-furyl arachidonoyl analog that acts as a potent and selective reuptake inhibitor of AEA (IC50 = 0.8 µM) but has low affinity for FAAH (IC50 = 30 µM); potentiates the biological effects of AEA when co-administered in rats.
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