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Enantiomeric cannabinoids: stereospecificity of psychotropic activity
Authors:R Mechoulam  J J Feigenbaum  N Lander  M Segal  T U J?rbe  A J Hiltunen  P Consroe
Institution:Brettler Medical Research Center, Faculty of Medicine, Hebrew University, Jerusalem, Israel.
Abstract:The 1,1-dimethylheptyl homolog of (-)-(3R,4R)-7-hydroxy-delta-6- tetrahydrocannabinol (compound II) is highly psychotropic in mice, rats and pigeons. The (+)-(3S,4S) enantiomer (III) was found to be psychotropically inactive at doses up to several thousand times those of the ED50 of (II).
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