|Chemical and physical data|
|Molar mass||313.445 g·mol−1|
|3D model (JSmol)|
MEPIRAPIM is an indole-based cannabinoid which differs from JWH-018 by having a 4-methylpiperazine group in place of the naphthyl group and has been used as an active ingredient in synthetic cannabis products. It was first identified in Japan in 2013, alongside FUBIMINA. MEPIRAPIM acts as a T-type calcium channel inhibitor and is only minimally active at the central CB1 receptor.
Sweden's public health agency suggested to classify MEPIRAPIM as hazardous substance on November 10, 2014.
- "MEPIRAPIM". Cayman Chemical. Retrieved 23 June 2015.
- Uchiyama N, Shimokawa Y, Matsuda S, Kawamura M, Kikura-Hanajiri R, Goda Y (January 2014). "Two new synthetic cannabinoids, AM-2201 benzimidazole analog (FUBIMINA) and (4-methylpiperazin-1-yl)(1-pentyl-1H-indol-3-yl)methanone (MEPIRAPIM), and three phenethylamine derivatives, 25H-NBOMe 3,4,5-trimethoxybenzyl analog, 25B-NBOMe, and 2C-N-NBOMe, identified in illegal products". Forensic Toxicology. 32 (1): 105–115. doi:10.1007/s11419-013-0217-2. S2CID 32599561.
- Kevin, Richard C.; Mirlohi, Somayeh; Manning, Jamie J.; Boyd, Rochelle; Cairns, Elizabeth A.; Ametovski, Adam; Lai, Felcia; Luo, Jia Lin; Jorgensen, William; Ellison, Ross; Gerona, Roy R.; Hibbs, David E.; McGregor, Iain S.; Glass, Michelle; Connor, Mark; Bladen, Chris; Zamponi, Gerald W.; Banister, Samuel D. (April 2022). "Putative Synthetic Cannabinoids MEPIRAPIM, 5F-BEPIRAPIM (NNL-2), and Their Analogues Are T-Type Calcium Channel (CaV3) Inhibitors". ACS Chemical Neuroscience. doi:10.1021/acschemneuro.1c00822. PMID 35442021.
- "Cannabinoider föreslås bli klassade som hälsofarlig vara". Retrieved 29 June 2015.