(C9)-CP 47,497
| Legal status | |
|---|---|
| Legal status |
|
| Identifiers | |
IUPAC name
| |
| CAS Number | |
| PubChem CID | |
| ChemSpider | |
| UNII | |
| CompTox Dashboard (EPA) | |
| Chemical and physical data | |
| Formula | C23H38O2 |
| Molar mass | 346.555 g·mol−1 |
| 3D model (JSmol) | |
SMILES
| |
InChI
| |
(C9)-CP 47,497 (CP 47,497 dimethylnonyl homologue) is a synthetic cannabinoid, a CP 47,497 homologue.[1]
Its systematic name is 2-[(1S,3R)-3-hydroxycyclohexyl]-5-(1,1-dimethylnonyl)phenol.
See also
- Synthetic cannabis
- (C6)-CP 47,497
- (C7)-CP 47,497 (CP 47,497 itself)
- (C8)-CP 47,497
References
- ^ Helander A (January 2017). "Synthetic Cannabinoid Receptor Agonists (Spice) as New Recreational Psychoactive Substances.". In Preedy VR (ed.). Handbook of Cannabis and Related Pathologies. London, United Kingdom: Academic Press. pp. 839-847 (843). ISBN 978-0-12-800827-0.
| Phytocannabinoids (comparison) |
| ||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Endocannabinoids |
| ||||||||||||||||||||||||||||||||||||||||
| Synthetic cannabinoid receptor agonists / neocannabinoids |
| ||||||||||||||||||||||||||||||||||||||||
| Allosteric CBRTooltip Cannabinoid receptor ligands | |||||||||||||||||||||||||||||||||||||||||
| Endocannabinoid enhancers (inactivation inhibitors) |
| ||||||||||||||||||||||||||||||||||||||||
| Anticannabinoids (antagonists/inverse agonists/antibodies) |
| ||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||
This article is issued from Wikipedia. The text is available under Creative Commons Attribution-Share Alike 4.0 unless otherwise noted. Additional terms may apply for the media files.