List of CP cannabinoids

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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).^[1] Recently, several members of this class of cannabinoids have been discovered in recreational drug products.^[2]^[3]^[4]

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.^[5]^[6]^[7]
(+)-CP 55,940 —
(-)-CP 55,940 —
CP-945,598 (Otenabant) —

References

↑ "Details for Synthetic cannabinoids". https://www.unodc.org/LSS/SubstanceGroup/Details/ae45ce06-6d33-4f5f-916a-e873f07bde02.
↑ Adams, Axel J.; Banister, Samuel D.; Irizarry, Lisandro; Trecki, Jordan; Schwartz, Michael; Gerona, Roy (2017-01-19). ""Zombie" Outbreak Caused by the Synthetic Cannabinoid AMB-FUBINACA in New York" (in en). New England Journal of Medicine 376 (3): 235–242. doi:10.1056/NEJMoa1610300. ISSN 0028-4793. http://www.nejm.org/doi/10.1056/NEJMoa1610300.
↑ "How Pfizer Helped Make Fake Pot" (in en). 2014-05-17. https://www.thedailybeast.com/how-pfizer-helped-make-spice-the-deadly-fake-pot/.
↑ Maia, J.; Fonseca, B. M.; Teixeira, N.; Correia-da-Silva, G. (2023-09-01). "Unveiling the angiogenic effects of cannabinoids: Enhancers or inhibitors?". Biochemical Pharmacology 215. doi:10.1016/j.bcp.2023.115686. ISSN 0006-2952. https://www.sciencedirect.com/science/article/pii/S0006295223002770.
↑ "CP 55,940" (in en). https://www.discoverx.com/catalog/cp-55-940/92-1343.
↑ Huffman, John W.; Thompson, Alicia L. S.; Wiley, Jenny L.; Martin, Billy R. (2008-01-01). "Synthesis and pharmacology of 1-deoxy analogs of CP-47,497 and CP-55,940". Bioorganic & Medicinal Chemistry. Nucleic Acid Modification for Fluroescence-Based Technologies 16 (1): 322–335. doi:10.1016/j.bmc.2007.09.033. ISSN 0968-0896. PMID 17919913. PMC 2262798. https://linkinghub.elsevier.com/retrieve/pii/S096808960700819X.
↑ "CP 55940, [Side Chain-2,3,4-3H(N)-, 25µCi (925kBq) | Revvity"]. https://www.revvity.com/product/cp55-940-side-chain-2-3-4-3h-n-net1051025uc.

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[1] "Details for Synthetic cannabinoids". https://www.unodc.org/LSS/SubstanceGroup/Details/ae45ce06-6d33-4f5f-916a-e873f07bde02.

[2] Adams, Axel J.; Banister, Samuel D.; Irizarry, Lisandro; Trecki, Jordan; Schwartz, Michael; Gerona, Roy (2017-01-19). ""Zombie" Outbreak Caused by the Synthetic Cannabinoid AMB-FUBINACA in New York" (in en). New England Journal of Medicine 376 (3): 235–242. doi:10.1056/NEJMoa1610300. ISSN 0028-4793. http://www.nejm.org/doi/10.1056/NEJMoa1610300.

[3] "How Pfizer Helped Make Fake Pot" (in en). 2014-05-17. https://www.thedailybeast.com/how-pfizer-helped-make-spice-the-deadly-fake-pot/.

[4] Maia, J.; Fonseca, B. M.; Teixeira, N.; Correia-da-Silva, G. (2023-09-01). "Unveiling the angiogenic effects of cannabinoids: Enhancers or inhibitors?". Biochemical Pharmacology 215. doi:10.1016/j.bcp.2023.115686. ISSN 0006-2952. https://www.sciencedirect.com/science/article/pii/S0006295223002770.

[5] "CP 55,940" (in en). https://www.discoverx.com/catalog/cp-55-940/92-1343.

[6] Huffman, John W.; Thompson, Alicia L. S.; Wiley, Jenny L.; Martin, Billy R. (2008-01-01). "Synthesis and pharmacology of 1-deoxy analogs of CP-47,497 and CP-55,940". Bioorganic & Medicinal Chemistry. Nucleic Acid Modification for Fluroescence-Based Technologies 16 (1): 322–335. doi:10.1016/j.bmc.2007.09.033. ISSN 0968-0896. PMID 17919913. PMC 2262798. https://linkinghub.elsevier.com/retrieve/pii/S096808960700819X.

[7] "CP 55940, [Side Chain-2,3,4-3H(N)-, 25µCi (925kBq) | Revvity"]. https://www.revvity.com/product/cp55-940-side-chain-2-3-4-3h-n-net1051025uc.

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List of CP cannabinoids

Topic: Chemistry

See also

References