A CB analog with a methyl group in the (R) configuration at C-2 of the ethanolamine group is not a FAAH inhibitor and is nearly as susceptible to amide hydrolysis as AEA itself.
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A CB analog with a methyl group in the (R) configuration at C-2 of the ethanolamine group; is not a FAAH inhibitor and is nearly as susceptible to amide hydrolysis as AEA itself.
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