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4-HO-PiPT

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
4-HO-PiPT
Clinical data
Other names4-Hydroxy-N-propyl-N-isopropyltryptamine; Piprocin
Routes of
administration
Oral
Drug classNon-selectiveserotonin receptor agonist;Serotonin5-HT2A receptoragonist;Serotonergic psychedelic;Hallucinogen
Identifiers
  • 3-{2-[(propan-2-yl)(propyl)amino]ethyl}-1H-indol-4-ol
CAS Number
PubChemCID
Chemical and physical data
FormulaC16H24N2O
Molar mass260.381 g·mol−1
3D model (JSmol)
  • CC(C)N(CCC)CCc1c[NH]c2cccc(O)c21
  • InChI=1S/C16H24N2O/c1-4-9-18(12(2)3)10-8-13-11-17-14-6-5-7-15(19)16(13)14/h5-7,11-12,17,19H,4,8-10H2,1-3H3
  • Key:CUTUPKOZXNFVHK-UHFFFAOYSA-N

4-HO-PiPT, also known as4-hydroxy-N-propyl-N-isopropyltryptamine or aspiprocin, is asubstituted tryptamine derivative which is claimed to havepsychedelic effects.[1] It has been encountered as a noveldesigner drug.[2]

Use and effects

[edit]

4-HO-EPT was not included nor mentioned inAlexander Shulgin's bookTiHKAL (Tryptamines I Have Known and Loved).[3]

Interactions

[edit]
See also:Psychedelic drug § Interactions, andTrip killer § Serotonergic psychedelic antidotes

Pharmacology

[edit]

Pharmacodynamics

[edit]

4-HO-PiPT acts as aserotonin5-HT2A receptoragonist, with anEC50Tooltip half-maximal effective concentration of 13.8 nM and anefficacy of 104.8%.[4]

Chemistry

[edit]

Analogues

[edit]

Analogues of 4-HO-PiPT includepropylisopropyltryptamine (PiPT),5-MeO-PiPT,4-HO-MiPT,4-HO-EiPT,4-HO-EiBT,4-HO-DiPT,4-HO-DsBT,4-HO-McPT, and4-HO-McPeT, among others.

History

[edit]

4-HO-PiPT has been sold as adesigner drug, first being identified in 2021 inBritish Columbia,Canada.[2]

See also

[edit]

References

[edit]
  1. ^Morrison J. Glycosylated psilocin derivatives and methods of use. WO 2024/042239A1
  2. ^abKnill A, Tobias S, Matthews J, Ti L (June 2022).A Report on British Columbia's Unregulated Drug Supply. Drug checking trends across British Columbia, January to December 2021(PDF).British Columbia Centre on Substance Use (Report).
  3. ^Shulgin A,Shulgin A (September 1997).TiHKAL: The Continuation.Berkeley, California:Transform Press.ISBN 0-9630096-9-9.OCLC 38503252.
  4. ^Banister S, Jorgensen W, Jinlong T. Compounds. Patent WO 2023/115167

External links

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