Chemistry:CP 42,096

From HandWiki
Short description: Chemical compound
CP 42,096
CP42096 structure.png
Identifiers
PubChem CID
Chemical and physical data
FormulaC26H34O4
Molar mass410.554 g·mol−1
3D model (JSmol)

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

  1. "Nonclassical cannabinoid analgetics inhibit adenylate cyclase: development of a cannabinoid receptor model". Molecular Pharmacology 33 (3): 297–302. March 1988. PMID 3352594. 
  2. "The evaluation of synthetic cannabimimetic congeners for discriminative stimulus and cataleptogenic effects in rats". NIDA Research Monograph 105: 421. 1990. OCLC 7457082. PMID 1652087. 
  3. "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. 
  4. "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. 
  5. "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.