5F-PCN
From Wikipedia, the free encyclopedia
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Identifiers | |
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CAS Number | None |
ChemSpider | 34450856 |
Chemical and physical data | |
Formula | C23H22FN3O |
Molar mass | 375.4 g/mol |
3D model (Jmol) | Interactive image |
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5F-PCN (also known as 5-F-MN-21) is an azaindole-based synthetic cannabinoid that is presumed to be a potent agonist of the CB1 receptor and has been sold online as a designer drug.[1][2] It is closely related to NNE1. Given the known metabolic liberation (and presence as an impurity) of amantadine in the related compound APINACA, it is suspected that metabolic hydrolysis of the amide group of 5F-PCN may release 1-naphthylamine, a known carcinogen.
Legal status[edit]
Sweden's public health agency suggested to classify 5F-PCN as hazardous substance on November 10, 2014.[3]
See also[edit]
References[edit]
- ^ "5F-PCN". Cayman Chemical. Retrieved 22 July 2015.
- ^ Antoni R. Blaazer; et al. (October 2011). "Novel indole and azaindole (pyrrolopyridine) cannabinoid (CB) receptor agonists: Design, synthesis, structure–activity relationships, physicochemical properties and biological activity". European Journal of Medicinal Chemistry. 46 (10): 5086–5098. doi:10.1016/j.ejmech.2011.08.021. PMID 21885167.
- ^ "Cannabinoider föreslås bli klassade som hälsofarlig vara". Folkhälsomyndigheten. Retrieved 22 July 2015.
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