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PX-1

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
PX-1
Legal status
Legal status
Identifiers
  • (S)-N-(1-amino-1-oxo-3-phenylpropan-2-yl)-1-(5-fluoropentyl)-1H-indole-3-carboxamide
CAS Number
PubChemCID
ChemSpider
UNII
Chemical and physical data
FormulaC23H26FN3O2
Molar mass395.478 g·mol−1
3D model (JSmol)
  • O=C(N[C@H](C(N)=O)CC1=CC=CC=C1)C2=CN(CCCCCF)C3=C2C=CC=C3
  • InChI=1S/C23H26FN3O2/c24-13-7-2-8-14-27-16-19(18-11-5-6-12-21(18)27)23(29)26-20(22(25)28)15-17-9-3-1-4-10-17/h1,3-6,9-12,16,20H,2,7-8,13-15H2,(H2,25,28)(H,26,29)/t20-/m0/s1
  • Key:DDVANTXQCRMRFF-FQEVSTJZSA-N

PX-1 (also known as5F-APP-PICA andSRF-30) is anindole-basedsynthetic cannabinoid that has been sold online as adesigner drug.[1][2][3]

Legality

[edit]

Sweden's public health agency suggested classifying PX-1 as hazardous substance on November 10, 2014.[4]

PX-1 is listed in the Fifth Schedule of the Misuse of Drugs Act (MDA) and therefore illegal in Singapore as of May 2015.[5]

See also

[edit]

References

[edit]
  1. ^"PX 1". Cayman Chemical. Retrieved15 July 2015.
  2. ^Presley BC, Logan BK, Jansen-Varnum SA (March 2020). "Phase I metabolism of synthetic cannabinoid receptor agonist PX-1 (5F-APP-PICA) via incubation with human liver microsomes and UHPLC-HRMS".Biomedical Chromatography.34 (3) e4786.doi:10.1002/bmc.4786.PMID 31863591.S2CID 209435138.
  3. ^Dahm P, Thomas A, Rothschild MA, Thevis M, Mercer-Chalmers-Bender K (July 2022)."Phase I-metabolism studies of the synthetic cannabinoids PX-1 and PX-2 using three different in vitro models".Forensic Toxicology.40 (2):244–262.doi:10.1007/s11419-021-00606-6.PMC 9715525.PMID 36454402.S2CID 245540105.
  4. ^"Cannabinoider föreslås bli klassade som hälsofarlig vara" [Cannabinoids are proposed to be classified as dangerous to health] (in Swedish). Folkhälsomyndigheten. Retrieved16 July 2015.
  5. ^"Misuse of Drugs Act". Singapore Government. 30 April 2015. Retrieved24 July 2015.
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