Cannabinoid · Synthetic (research chemical)
CP-55,940 is a fully synthetic cannabinoid used in labs as a Pfizer reference agonist and potency benchmark, part of a class that is potent, unpredictable and linked to serious harm and deaths.
Where it fits
CP-55,940 derives from Synthetic. See the Synthetic & altered cannabinoids index for how it relates to the rest of the family.
What the research shows
Direct human research on CP-55,940 is minimal; it is characterised mainly by its chemistry and its place in the cannabinoid family rather than by clinical studies. We flag that plainly rather than overstate it.
Safety
A fully synthetic cannabinoid, covered for education and harm reduction only. Synthetic cannabinoids are potent, unpredictable and linked to serious harm and deaths. No synthesis, dose or source information appears on this site.
FAQ
Is CP-55,940 intoxicating? CP-55,940 is intoxicating.
Where does CP-55,940 come from? From Synthetic.
Why is CP-55,940 important in cannabinoid science? Radiolabeled [3H]-CP-55,940 was the molecular probe used in 1988 to discover and map the CB1 cannabinoid receptor in mammalian brain tissue.
Pfizer Non-Classical Synthesis, CB1/CB2 Receptor Discovery, and Pharmacology
CP-55,940 (C24H40O3) is a bicyclic non-classical synthetic cannabinoid developed by Pfizer in 1974 that lacks the dihydropyran ring of tricyclic delta-9-THC while acting as a high-affinity full agonist at both CB1 and CB2 receptors (Pertwee, 1999, PubMed PMID 1106801). Tritiated [3H]-CP-55,940 served as the radioligand that enabled Devane et al. to identify and characterize the brain cannabinoid receptor (CB1) in 1988 (Devane et al., 1988, PubMed PMID 2848184), and high-resolution X-ray crystallography later resolved the active-state human CB1 receptor in complex with agonists related to CP-55,940 (Hua et al., 2017, PubMed PMID 28678776); see also HU-210 and WIN 55,212-2.
Part of the NOIDS cannabinoids index. Educational reference, not medical advice.