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).
Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1007/BF01959156 | DOI Listing |
Publication Analysis
Top Keywords
enantiomeric cannabinoids
4
cannabinoids stereospecificity
4
stereospecificity psychotropic
4
psychotropic activity
4
activity 11-dimethylheptyl
4
11-dimethylheptyl homolog
4
homolog --3r4r-7-hydroxy-delta-6-
4
--3r4r-7-hydroxy-delta-6- tetrahydrocannabinol
4
tetrahydrocannabinol compound
4
compound highly
4
Similar Publications
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!