Adamantyl-THPINACA

Adamantyl-THPINACA
Legal status
Legal status	CA: Schedule II; DE: NpSG (Industrial and scientific use only); UK: Class B;
Identifiers
	IUPAC name N-(2-Adamantyl)-1-(tetrahydropyran-4-ylmethyl)indazole-3-carboxamide;
CAS Number	2365471-86-7 ; 1400742-48-4 (1-adamantyl isomer);
PubChem CID	123132009;
ChemSpider	58858889;
UNII	7I4LAF1R3Y;
CompTox Dashboard (EPA)	DTXSID101009995 ;
Chemical and physical data
Formula	C24H31N3O2
Molar mass	393.531 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES C12C(C3CC(CC(C1)C3)C2)NC(=O)C2=NN(C3=CC=CC=C23)CC2CCOCC2;
	InChI InChI=1/C24H31N3O2/c28-24(25-22-18-10-16-9-17(12-18)13-19(22)11-16)23-20-3-1-2-4-21(20)27(26-23)14-15-5-7-29-8-6-15/h1-4,15-19,22H,5-14H2,(H,25,28)/f/h25H; Key:XFZLBNDGZVRJNJ-UHFFFAOYSA-N;

Adamantyl-THPINACA (ATHPINACA, AD-THPINACA)^[1] is an indazole-based synthetic cannabinoid,^[2] which was first reported to Europol in Slovenia in January 2015.^[3] It is known as both the 1-adamantyl and 2-adamantyl isomers (SGT-40 and SGT-194 respectively), which can be distinguished by GC-EI-MS.^[4] It is banned in Sweden^[5] and Russia.^[6] Both the 1-adamantyl and 2-adamantyl isomers are specifically listed as illegal drugs in Japan.^[7] 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 Adamantyl-THPINACA may also release amantadine.

Quick facts Legal status, Identifiers ...

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Adamantyl-THPINACA

See also

References

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