FDU-PB-22

FDU-PB-22

Systematic (IUPAC) name
naphthalen-1-yl 1-[(4-fluorophenyl)methyl]-1H-indole-3-carboxylate
Legal status
Legal status	CA: Schedule II DE: Anlage II (Prohibited)
Identifiers
ChemSpider	29763739
UNII	85E88884ZQ
Chemical data
Formula	C26H18FNO2
Molar mass	395.42 g/mol
SMILES O=C(OC1=C(C=CC=C2)C2=CC=C1)C3=CN(CC4=CC=C(F)C=C4)C5=C3C=CC=C5
InChI InChI=1S/C26H18FNO2/c27-20-14-12-18(13-15-20)16-28-17-23(22-9-3-4-10-24(22)28)26(29)30-25-11-5-7-19-6-1-2-8-21(19)25/h1-15,17H,16H2 Key:RCEKSVIFQKKFLS-UHFFFAOYSA-N

FDU-PB-22 is an derivative of JWH-018 that is presumed to be a potent agonist of the CB₁ receptor and has been sold online as a "legal high".^[1][2]

Legal status

FDU-PB-22 is a controlled substance in Germany and is banned in Japan and Sweden.^[3]

See also

• 5F-PB-22
• AM-2201
• BB-22
• FUB-JWH-018
• AB-FUBINACA
• ADB-FUBINACA
• AMB-FUBINACA
• FUB-144
• FUB-APINACA
• FUB-NNE1
• FUB-PB-22
• MDMB-FUBICA
• MDMB-FUBINACA
• PB-22

References

1. "FDU-PB-22". Southern Association of Forensic Scientists. Retrieved 23 July 2015.
2. Nahoko Uchiyama, Yoshihiko Shimokawa, Ruri Kikura-Hanajiri, Yosuke Demizu, Yukihiro Goda, Takashi Hakamatsuka (February 2015). "A synthetic cannabinoid FDU-NNEI, two 2H-indazole isomers of synthetic cannabinoids AB-CHMINACA and NNEI indazole analog (MN-18), a phenethylamine derivative N–OH-EDMA, and a cathinone derivative dimethoxy-α-PHP, newly identified in illegal products". Forensic Toxicology. doi:10.1007/s11419-015-0268-7.
3. "Cannabinoider föreslås bli klassificerade som hälsofarlig vara". Folkhälsomyndigheten. 28 May 2014. Retrieved 23 July 2015.