Chemistry:JWH-366
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| Formula | C25H24N2O |
| Molar mass | 368.480 g·mol−1 |
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JWH-366 (naphthalen-1-yl-(1-pentyl-5-pyridin-3-ylpyrrol-3-yl)methanone) is a synthetic cannabinoid from the naphthoylpyrrole family which acts as an agonist of the CB1 (Ki = 191 ± 12nM) and CB2 (Ki = 24 ± 1nM) receptors, with a strong (~8x) selectivity for the CB2 receptor over the CB1 receptor. JWH-366 was first synthesized in 2006 by John W. Huffman and colleagues to examine the nature of ligand binding to the CB1 receptor.[1]
Legality
In the United States JWH-366 is not federally scheduled, although some states have passed legislation banning the sale, possession, and manufacture of JWH-366.[2][3][4][5]
In Canada, JWH-366 and other naphthoylpyrrole-based cannabinoids are Schedule II controlled substances under the Controlled Drugs and Substances Act.
In the United Kingdom, JWH-366 and other naphthoylpyrrole-based cannabinoids are considered Class B drugs under the Misuse of Drugs Act 1971.
See also
- List of JWH cannabinoids
- Synthetic cannabinoid
References
- ↑ "1-Alkyl-2-aryl-4-(1-naphthoyl)pyrroles: new high affinity ligands for the cannabinoid CB1 and CB2 receptors". Bioorganic & Medicinal Chemistry Letters 16 (20): 5432–5. October 2006. doi:10.1016/j.bmcl.2006.07.051. PMID 16889960.
- ↑ : Schedules of controlled substances
- ↑ "The 2020 Florida Statutes". http://www.leg.state.fl.us/Statutes/index.cfm?App_mode=Display_Statute&URL=0800-0899/0893/Sections/0893.03.html.
- ↑ "Arizona Revised Statutes Title 13. Criminal Code § 13-3401". https://www.azleg.gov/ars/13/03401.htm.
- ↑ "California Code, Health and Safety Code - HSC § 11357.5". https://codes.findlaw.com/ca/health-and-safety-code/hsc-sect-11357-5.html.
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