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).{{Cite web |title=Details for Synthetic cannabinoids |url=https://www.unodc.org/LSS/SubstanceGroup/Details/ae45ce06-6d33-4f5f-916a-e873f07bde02 |access-date=2025-04-26 |website=www.unodc.org}} Recently, several members of this class of cannabinoids have been discovered in recreational drug products.{{Cite journal |last=Adams |first=Axel J. |last2=Banister |first2=Samuel D. |last3=Irizarry |first3=Lisandro |last4=Trecki |first4=Jordan |last5=Schwartz |first5=Michael |last6=Gerona |first6=Roy |date=2017-01-19 |title=“Zombie” Outbreak Caused by the Synthetic Cannabinoid AMB-FUBINACA in New York |url=http://www.nejm.org/doi/10.1056/NEJMoa1610300 |journal=New England Journal of Medicine |language=en |volume=376 |issue=3 |pages=235–242 |doi=10.1056/NEJMoa1610300 |issn=0028-4793}}{{Cite web |date=2014-05-17 |title=How Pfizer Helped Make Fake Pot |url=https://www.thedailybeast.com/how-pfizer-helped-make-spice-the-deadly-fake-pot/ |access-date=2025-04-26 |website=The Daily Beast |language=en}}{{Cite journal |last=Maia |first=J. |last2=Fonseca |first2=B. M. |last3=Teixeira |first3=N. |last4=Correia-da-Silva |first4=G. |date=2023-09-01 |title=Unveiling the angiogenic effects of cannabinoids: Enhancers or inhibitors? |url=https://www.sciencedirect.com/science/article/pii/S0006295223002770 |journal=Biochemical Pharmacology |volume=215 |pages=115686 |doi=10.1016/j.bcp.2023.115686 |issn=0006-2952|doi-access=free }}

• 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.{{Cite web |title=CP 55,940 |url=https://www.discoverx.com/catalog/cp-55-940/92-1343 |access-date=2025-04-26 |website=localhost |language=en}}{{Cite journal |last=Huffman |first=John W. |last2=Thompson |first2=Alicia L. S. |last3=Wiley |first3=Jenny L. |last4=Martin |first4=Billy R. |date=2008-01-01 |title=Synthesis and pharmacology of 1-deoxy analogs of CP-47,497 and CP-55,940 |url=https://linkinghub.elsevier.com/retrieve/pii/S096808960700819X |journal=Bioorganic & Medicinal Chemistry |series=Nucleic Acid Modification for Fluroescence-Based Technologies |volume=16 |issue=1 |pages=322–335 |doi=10.1016/j.bmc.2007.09.033 |issn=0968-0896 |pmc=2262798 |pmid=17919913}}{{Cite web |title=CP 55940, [Side Chain-2,3,4-3H(N)]-, 25µCi (925kBq) {{!}} Revvity |url=https://www.revvity.com/product/cp55-940-side-chain-2-3-4-3h-n-net1051025uc |access-date=2025-04-26 |website=www.revvity.com}}
• (+)-CP 55,940 —
• (-)-CP 55,940 —
• CP-945,598 (Otenabant) —