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4-AcO-MPT

From Wikipedia, the free encyclopedia

Pharmaceutical compound
4-AcO-MPT
Clinical data
Other names4-Acetoxy-MPT; 4-Acetoxy-N-methyl-N-propyltryptamine
Routes of
administration
Oral
Drug classNon-selectiveserotonin receptor agonist;Serotonin5-HT2A receptoragonist;Serotonergic psychedelic;Hallucinogen
ATC code
  • None
Identifiers
  • [3-[2-[methyl(propyl)amino]ethyl]-1H-indol-4-yl] acetate
CAS Number
PubChemCID
ChemSpider
UNII
Chemical and physical data
FormulaC16H22N2O2
Molar mass274.364 g·mol−1
3D model (JSmol)
  • CCCN(C)CCC1=CNC2=C1C(=CC=C2)OC(=O)C
  • InChI=1S/C16H22N2O2/c1-4-9-18(3)10-8-13-11-17-14-6-5-7-15(16(13)14)20-12(2)19/h5-7,11,17H,4,8-10H2,1-3H3
  • Key:CECCEKYTLKWWJJ-UHFFFAOYSA-N

4-AcO-MPT, also known as4-acetoxy-N-methyl-N-propyltryptamine, is apsychedelic drug of thetryptamine and4-hydroxytryptamine families related to4-AcO-DMT (psilacetin).[1][2][3][4][5]

Use and effects

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See also:4-HO-MPT § Use and effects

Interactions

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

Pharmacology

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Pharmacodynamics

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4-AcO-MPT is thought to act as aprodrug of4-HO-MPT and hence is believed to act as anon-selectiveserotonin receptor agonist including of theserotonin5-HT2A receptor.[3][4] Thereceptor interactions of 4-AcO-MPT have been studied.[6] The drug produces thehead-twitch response, a behavioral proxy of psychedelic effects, in rodents,[4]

Chemistry

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Analogues

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Analogues of 4-AcO-MPT includemethylpropyltryptamine (MPT),4-HO-MPT (meprocin),5-MeO-MPT,4-AcO-DMT (psilacetin),4-AcO-MET (metacetin),4-AcO-MiPT (mipracetin), and4-AcO-DPT (depracetin), among others.

History

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4-AcO-MPT was first described in thescientific literature by at least 2017.[2] It was first encountered as a noveldesigner drug in 2018.[1]

Society and culture

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Legal status

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Canada

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4-AcO-MPT is not acontrolled substance inCanada as of 2025.[7]

Sweden

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4-AcO-MPT is acontrolled substance inSweden.[8]

See also

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References

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  1. ^ab"4-AcO-MPT".АИПСИН (in Russian). Retrieved11 October 2025.
  2. ^abChapman S (31 December 2017).PeakAL: Protons I Have Known and Loved, Too — Another Fifty Shades of Grey-Market Spectra(PDF) (Report).doi:10.16889/isomerdesign-5. Retrieved11 October 2025.
  3. ^abBerardinelli D, Montanari E, Malaca S, Zaami S, Busardò FP, Huestis MA, et al. (2022)."4-Hydroxy-N,N-methylpropyltryptamine (4-OH-MPT) in vitro human metabolism".Toxicologie Analytique et Clinique.34 (3): S96.Bibcode:2022ToxAC..34Q..96B.doi:10.1016/j.toxac.2022.06.147.
  4. ^abcKlein AK, Chatha M, Laskowski LJ, Anderson EI, Brandt SD, Chapman SJ, et al. (April 2021)."Investigation of the Structure-Activity Relationships of Psilocybin Analogues".ACS Pharmacology & Translational Science.4 (2):533–542.doi:10.1021/acsptsci.0c00176.PMC 8033608.PMID 33860183.
  5. ^Glatfelter GC, Naeem M, Pham DN, Golen JA, Chadeayne AR, Manke DR, et al. (April 2023)."Receptor Binding Profiles for Tryptamine Psychedelics and Effects of 4-Propionoxy-N,N-dimethyltryptamine in Mice".ACS Pharmacology & Translational Science.6 (4):567–577.doi:10.1021/acsptsci.2c00222.PMC 10111620.PMID 37082754.
  6. ^Glatfelter GC, Naeem M, Pham DN, Golen JA, Chadeayne AR, Manke DR, et al. (April 2023)."Receptor Binding Profiles for Tryptamine Psychedelics and Effects of 4-Propionoxy-N,N-dimethyltryptamine in Mice".ACS Pharmacol Transl Sci.6 (4):567–577.doi:10.1021/acsptsci.2c00222.PMC 10111620.PMID 37082754.
  7. ^"Controlled Drugs and Substances Act".Department of Justice Canada. Retrieved19 January 2026.
  8. ^"4-AcO-MPT".АИПСИН (in Russian). Retrieved2 January 2026.

External links

[edit]
Tryptamines
No ring subs.
4-Hydroxytryptamines
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α-Alkyltryptamines
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Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
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Cyclized tryptamines
Isotryptamines
Related compounds
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