DescriptionMetabolically stable inhibitor of anandamide cellular uptake (Ki = 3 µM). Displays relatively low affinity for CB1 and CB2 receptors (Ki values are 5.1 and > 10 µM) and for vanilloid VR1 receptors (EC50 = 10 µM). Has minimal activity against FAAH (Ki > 50 µM). Active in vivo.
|Observed MW: 431.66|
Safety and Handling
Recommended Storage : Store at +4°C
For Research Use Only
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