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4-HO-EPT

From Wikipedia, the free encyclopedia

Pharmaceutical compound
4-HO-EPT
Clinical data
Other names4-OH-EPT; 4-Hydroxy-N-ethyl-N-propyltryptamine; Eprocin
Routes of
administration
Oral
Drug classNon-selectiveserotonin receptor agonist;Serotonin5-HT2A receptoragonist;Serotonergic psychedelic;Hallucinogen
ATC code
  • None
Identifiers
  • 3-{2-[ethyl(propyl)amino]ethyl}-1H-indol-4-ol
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC15H22N2O
Molar mass246.354 g·mol−1
3D model (JSmol)
  • CCCN(CC)CCC1=CNC2=CC=CC(O)=C12
  • InChI=1S/C15H22N2O/c1-3-9-17(4-2)10-8-12-11-16-13-6-5-7-14(18)15(12)13/h5-7,11,16,18H,3-4,8-10H2,1-2H3
  • Key:JQELEPKHBXEAHR-UHFFFAOYSA-N

4-HO-EPT, also known as4-hydroxy-N-ethyl-N-propyltryptamine or aseprocin, is apsychedelic drug of thetryptamine family, which isstructurally related topsilocin (4-HO-DMT).[1] It was encountered as a noveldesigner drug inJapan by 2021.[1]

Use and effects

[edit]

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

Interactions

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

Pharmacology

[edit]

Pharmacodynamics

[edit]
4-HO-EPT activities
TargetAffinity (Ki, nM)
5-HT1A163
5-HT1B1,097
5-HT1D644
5-HT1E591
5-HT2A546 (Ki)
3.2 (EC50Tooltip half-maximal effective concentration)
100% (EmaxTooltip maximal efficacy)
5-HT2B62 (Ki)
4.3 (EC50)
89% (
Emax)
5-HT2C1,272 (Ki)
129 (EC50)
89% (
Emax)
5-HT5A1,576
5-HT6284
5-HT7438
α2A2,073
α2B,α2C>10,000
D23,010
D3985
D4,D5>10,000
H1406
H2>10,000
M4>10,000
σ11,400
σ21,773
KORTooltip κ-Opioid receptor>10,000
NR2B5,947
SERTTooltip Serotonin transporter1,257
DATTooltip Dopamine transporter>10,000
Notes: The smaller the value, the more avidly the drug interacts with the site.Sources:[3][4]

4-HO-EPT is apotentfull agonist of theserotonin5-HT2A,5-HT2B, and5-HT2C receptors.[3][4] It has one to two orders of magnitude greater potency as a serotonin 5-HT2A and 5-HT2B receptor agonist than as a serotonin 5-HT2C receptor agonist.[3] The drug also showsaffinity for otherserotonin receptors, such as the serotonin5-HT1A and5-HT6 receptors.[4] 4-HO-EPT produces thehead-twitch response, a behavioral proxy ofpsychedelic effects, in rodents.[3]

Pharmacokinetics

[edit]

Themetabolism of 4-HO-EPT has been studied.[5]

Chemistry

[edit]

Analogues

[edit]

Analogues of 4-HO-EPT includeethylpropyltryptamine (EPT),5-MeO-EPT,5-fluoro-EPT,4-HO-MPT,4-HO-PiPT,4-HO-DET, and4-HO-DPT, among others.

Society and culture

[edit]

Legal status

[edit]

United Kingdom

[edit]

4-HO-EPT is illegal in theUnited Kingdom as a result of thePsychoactive Substances Act of 2016.[6]

United States

[edit]

4-HO-EPT may be considered an analogue ofpsilocin, which is a Schedule I drug under theControlled Substances Act. As such, the sale for human consumption would be illegal under theFederal Analogue Act.[citation needed]

See also

[edit]

References

[edit]
  1. ^abTanaka R, Kawamura M, Hakamatsuka T, Kikura-Hanajiri R (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.ISSN 1860-8965. Retrieved9 October 2025.
  2. ^Shulgin A,Shulgin A (September 1997).TiHKAL: The Continuation.Berkeley, California:Transform Press.ISBN 0-9630096-9-9.OCLC 38503252.
  3. ^abcdKlein 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.
  4. ^abcGlatfelter 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.
  5. ^Bergh MS, Bogen IL, Grafinger KE, Huestis MA, Øiestad ÅM (December 2024)."Metabolite markers for three synthetic tryptamines N-ethyl-N-propyltryptamine, 4-hydroxy-N-ethyl-N-propyltryptamine, and 5-methoxy-N-ethyl-N-propyltryptamine".Drug Testing and Analysis.16 (12):1544–1557.doi:10.1002/dta.3668.PMC 11635065.PMID 38459837.
  6. ^"Misuse of Drugs Act 1971 (Legislation.gov.uk)".

External links

[edit]
Tryptamines
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