From Wikipedia, the free encyclopedia
Many synthetic
cannabinoids were designed by Pfizer in the 1970s and 1980s, and feature an alphanumeric code beginning with the prefix "CP" (after
Charles Pfizer ). Recently, several members of this class of cannabinoids have been discovered in recreational drug products.
CP 47,497 —
(C6)-CP 47,497 —
(C7)-CP 47,497 (CP 47,497 itself) —
(C8)-CP 47,497 (Cannabicyclohexanol) —
(C9)-CP 47,497 —
CP 50,556-1 (Levonantradol) —
CP 55,244 —
CP 55,940 —
(±)-CP 55,940 — (±)-CP 55,940 is a widely used cannabinoid research tool.
(+)-CP 55,940 —
(-)-CP 55,940 —
CP-945,598 (Otenabant) —
See also
References
Phytocannabinoids (
comparison )
Cannabibutols Cannabichromenes Cannabicyclols Cannabidiols Cannabielsoins Cannabigerols Cannabiphorols Cannabinols Cannabitriols Cannabivarins Delta-8-tetrahydrocannabinols Delta-9-tetrahydrocannabinols Delta-10-Tetrahydrocannabinols Miscellaneous cannabinoids Active metabolites
Endocannabinoids
Synthetic cannabinoid receptor agonists / neocannabinoids
Classical cannabinoids (dibenzopyrans) Non-classical cannabinoids Adamantoylindoles Benzimidazoles Benzoylindoles Cyclohexylphenols
Eicosanoids
Hydrocarbons Indazole carboxamides Indazole-3- carboxamides Indole-3-carboxamides Indole-3-carboxylates Naphthoylindazoles
Naphthoylindoles Naphthoylpyrroles Naphthylmethylindenes Naphthylmethylindoles Phenylacetylindoles Pyrazolecarboxamides Pyrrolobenzoxazines Quinolinyl esters Tetramethylcyclo- propanoylindazoles Tetramethylcyclo- propanoylindoles Tetramethylcyclo- propylindoles Others
Allosteric
CBR Tooltip Cannabinoid receptor
ligands
Endocannabinoid enhancers (inactivation inhibitors)
Anticannabinoids (antagonists/inverse agonists/antibodies)