CUMYL-PINACA

CUMYL-PINACA
Legal status
Legal status	CA: Schedule II; DE: NpSG (Industrial and scientific use only); UK: Class B;
Identifiers
	IUPAC name 1-pentyl-N-(2-phenylpropan-2-yl)-1H-indazole-3-carboxamide;
CAS Number	1400742-15-5 ;
PubChem CID	86273676;
ChemSpider	48060412;
UNII	3N1P3KD3CV;
CompTox Dashboard (EPA)	DTXSID001019036 ;
Chemical and physical data
Formula	C22H27N3O
Molar mass	349.478 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CCCCCN1N=C(C(=O)NC(C)(C)C2=CC=CC=C2)C2=CC=CC=C12;
	InChI InChI=1S/C22H27N3O/c1-4-5-11-16-25-19-15-10-9-14-18(19)20(24-25)21(26)23-22(2,3)17-12-7-6-8-13-17/h6-10,12-15H,4-5,11,16H2,1-3H3,(H,23,26); Key:LCBASRYREGWIJT-UHFFFAOYSA-N;

CUMYL-PINACA (also known as SGT-24) is an indazole-3-carboxamide based synthetic cannabinoid. CUMYL-PINACA acts as a potent agonist for the cannabinoid receptors, with approximately 3x selectivity for CB₁, having an EC₅₀ of 0.15nM for human CB₁ receptors and 0.41nM for human CB₂ receptors.^[1] In its pure form, it is described as a sticky oil which can cause poisoning through transdermal exposure.^[2]

Legal status

Sweden's public health agency suggested classifying CUMYL-PINACA as a hazardous substance, on November 10, 2014.^[3]

^ Bowden; et al. (11 April 2013). "Patent WO 2014167530 - Cannabinoid compounds". New Zealand Patent application 623626. Retrieved 11 July 2015.
^ Dobaja M, Grenc D, Kozelj G, Brvar M (March 2017). "Occupational transdermal poisoning with synthetic cannabinoid cumyl-PINACA". Clinical Toxicology. 55 (3): 193–195. doi:10.1080/15563650.2016.1278224. PMID 28084855. S2CID 21304629.
^ "Cannabinoider föreslås bli klassade som hälsofarlig vara". Retrieved 11 July 2015.

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