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Ethylpropyltryptamine

From Wikipedia, the free encyclopedia

Pharmaceutical compound
Ethylpropyltryptamine
Clinical data
Other namesEPT;N-Ethyl-N-propyltryptamine
Drug classSerotonergic psychedelic;Hallucinogen
ATC code
  • None
Identifiers
  • N-ethyl-N-[2-(1H-indol-3-yl)ethyl]propan-1-amine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC15H22N2
Molar mass230.355 g·mol−1
3D model (JSmol)
  • CCCN(CC)CCC1=CNC2=CC=CC=C12
  • InChI=1S/C15H22N2/c1-3-10-17(4-2)11-9-13-12-16-15-8-6-5-7-14(13)15/h5-8,12,16H,3-4,9-11H2,1-2H3
  • Key:LCDYRMYSOIVPRS-UHFFFAOYSA-N

Ethylpropyltryptamine (EPT), also known asN-ethyl-N-propyltryptamine, is a rarely encounteredpsychedelic drug in thetryptamine family. It has been identified in illicit products in Japan.[1]

Use and effects

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EPT was not included nor mentioned inAlexander Shulgin's bookTiHKAL (Tryptamines I Have Known and Loved).[2]

Interactions

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

Chemistry

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Analogues

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Analogues of EPT includemethylethyltryptamine (MET),methylpropyltryptamine (MPT),diethyltryptamine (DET),dipropyltryptamine (DPT), among others.[2]

Society and culture

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Legal status

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United Kingdom

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It is illegal to sell, distribute, supply, transport or trade the pharmaceutical drug under thePsychoactive Substances Act of 2016.[3]

United States

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EPT is unscheduled but it may be considered an analogue of DMT, which is a Schedule I drug under theControlled Substances Act. As such, the sale for human consumption could be illegal under theFederal Analogue Act.

See also

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References

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  1. ^Tanaka R, Kawamura M, Hakamatsuka T, Kikura-Hanajiri R (January 2021). "Identification of six tryptamine derivatives as designer drugs in illegal products".Forensic Toxicology.39 (1):248–258.doi:10.1007/s11419-020-00556-5.
  2. ^abShulgin A,Shulgin A (September 1997).TiHKAL: The Continuation.Berkeley, California:Transform Press.ISBN 0-9630096-9-9.OCLC 38503252.
  3. ^"Misuse of Drugs Act 1971".Legislation.gov.uk.

External links

[edit]
Tryptamines
No ring subs.
4-Hydroxytryptamines
5-Hydroxytryptamines
5-Methoxytryptamines
Other ring subs.
α-Alkyltryptamines
Others
Cyclized
Bioisosteres
Phenethylamines
Scalines
2C-x
3C-x
DOx
4C-x
Ψ-PEA
MDxx
FLY
25x-NB (NBOMes)
Others
Cyclized
Lysergamides
  • Bioisosteres:JRT
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Natural sources
Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
Cyclized tryptamines
Isotryptamines
Related compounds
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