5F-CUMYL-PEGACLONE Legal status
UK : Under Psychoactive Substances Act
2,5-Dihydro-2-(1-methyl-1-phenylethyl)-5-(5-fluoropentyl)-1H-pyrido[4,3-b]indol-1-one
PubChem CID Formula C 25 H 27 F N 2 O Molar mass 390.49 g·mol−1 3D model (JSmol )
CC(C)(c1ccccc1)N4C=Cc3n(CCCCCF)c2ccccc2c3C4=O
InChI=1S/C25H27FN2O/c1-25(2,19-11-5-3-6-12-19)28-18-15-22-23(24(28)29)20-13-7-8-14-21(20)27(22)17-10-4-9-16-26/h3,5-8,11-15,18H,4,9-10,16-17H2,1-2H3
Key:SMRRORRDOWXERZ-UHFFFAOYSA-N
5F-CUMYL-PEGACLONE (5F-SGT-151 , SGT-269 ) is a gamma-carboline based synthetic cannabinoid that has been sold as a designer drug , first being identified in Germany in 2017. It acts as a potent full agonist of the CB1 receptor. [1] [2] It appears to be more toxic than related compounds such as CUMYL-PEGACLONE , and has been linked to numerous serious adverse reactions, some fatal.[3]
See also [ ]
5F-CUMYL-PINACA
CUMYL-5F-P7AICA
References [ ]
^ Mogler L, Halter S, Wilde M, Franz F, Auwärter V (2019). "Human phase I metabolism of the novel synthetic cannabinoid 5F-CUMYL-PEGACLONE" . Forensic Toxicology . 37 (1): 154–163. doi :10.1007/s11419-018-0447-4 . PMC 6315001 . PMID 30636984 .
^ Janssens L, Cannaert A, Connolly MJ, Liu H, Stove CP (June 2020). "In vitro activity profiling of Cumyl-PEGACLONE variants at the CB1 receptor: Fluorination versus isomer exploration". Drug Testing and Analysis . 12 (9): 1336–1343. doi :10.1002/dta.2870 . hdl :1854/LU-8687072 . PMID 32490586 . S2CID 219285656 .
^ Giorgetti A, Mogler L, Halter S, Haschimi B, Alt A, Rentsch D, Schmidt B, Thoma V, Vogt S, Auwärter V (2019). "Four cases of death involving the novel synthetic cannabinoid 5F-Cumyl-PEGACLONE" . Forensic Toxicology . 38 (2): 314–326. doi :10.1007/s11419-019-00514-w . S2CID 209449526 .
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Cannabinoids (cannabinoids by structure)