Chemistry:CP 42,096
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Short description: Chemical compound
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PubChem CID | |
Chemical and physical data | |
Formula | C26H34O4 |
Molar mass | 410.554 g·mol−1 |
3D model (JSmol) | |
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CP 42,096 is an analgesic drug which acts as a cannabinoid agonist. It was developed by Pfizer in the 1980s as part of the research that led to the development of levonantradol,[1][2][3] and is more potent than THC but less potent than newer compounds such as CP 55,244.[4][5]
See also
References
- ↑ "Nonclassical cannabinoid analgetics inhibit adenylate cyclase: development of a cannabinoid receptor model". Molecular Pharmacology 33 (3): 297–302. March 1988. PMID 3352594.
- ↑ "The evaluation of synthetic cannabimimetic congeners for discriminative stimulus and cataleptogenic effects in rats". NIDA Research Monograph 105: 421. 1990. OCLC 7457082. PMID 1652087.
- ↑ "Levonantradol". Marihuana and Medicine.. Totowa, NJ: Humana Press. 1999. pp. 553–560. doi:10.1007/978-1-59259-710-9_53. ISBN 978-1-4757-5717-0.
- ↑ "Enhancement of brain [3H]flunitrazepam binding and analgesic activity of synthetic cannabimimetics". European Journal of Pharmacology 109 (2): 201–12. February 1985. doi:10.1016/0014-2999(85)90421-2. PMID 2986995.
- ↑ "Hexahydrocannabinol (HHC) and related substances.". European Monitoring Centre for Drugs and Drug Addiction. 2023. https://www.emcdda.europa.eu/system/files/documents/2023-05/emcdda-technical-report-hhc-and-related-substances.pdf.
![]() | Original source: https://en.wikipedia.org/wiki/CP 42,096.
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