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3C-E

From Wikipedia, the free encyclopedia
Psychedelic drug

Pharmaceutical compound
3C-E
Clinical data
Other names4-Ethoxy-3,5-dimethoxyamphetamine; 3,5-Dimethoxy-4-ethoxyamphetamine; α-Methylescaline; 3C-Escaline
Routes of
administration
Oral[1][2][3][4]
Drug classSerotonin receptor modulator;Serotonin5-HT2A receptoragonist;Serotonergic psychedelic;Hallucinogen
Legal status
Legal status
Pharmacokinetic data
Duration of action8–12 hours[1][3]
Identifiers
  • 1-(4-Ethoxy-3,5-dimethoxyphenyl)propan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H21NO3
Molar mass239.315 g·mol−1
3D model (JSmol)
  • CCOc1c(cc(cc1OC)CC(C)N)OC
  • InChI=1S/C13H21NO3/c1-5-17-13-11(15-3)7-10(6-9(2)14)8-12(13)16-4/h7-9H,5-6,14H2,1-4H3
  • Key:AHLXCGRWNKUNTQ-UHFFFAOYSA-N

3C-E, also known as4-ethoxy-3,5-dimethoxyamphetamine or asα-methylescaline (3C-escaline), is apsychedelic drug of thephenethylamine,amphetamine, and3C families related to3,4,5-trimethoxyamphetamine (TMA).[1][5][3] It is the amphetamine (3C)analogue ofescaline.[1][3] The drug has a dose range of 30 to 60 mgorally, with a typical dose estimate of 45 mg, and aduration of 8 to 12 hours.[1][2][5][3][4] It has about the samepotency as escaline.[1][2][6] The drug is a potentserotonin5-HT2A receptoragonist and also interacts with otherserotonin receptors andtargets.[3][5] It produces thehead-twitch response, a behavioral proxy of psychedelic effects, in rodents.[7][4] 3C-E was first described in thescientific literature by Benington and colleagues in 1954.[8]Alexander Shulgin and colleagues reported an active dose of 40 mg based on unpublished findings in a 1978literature review.[9][10] Subsequently, Shulgin further reported the properties and effects of 3C-E in his 1991 bookPiHKAL (Phenethylamines I Have Known and Loved).[1] The drug was encountered as a noveldesigner drug inEurope in 2013.[11][12][7]

See also

[edit]

References

[edit]
  1. ^abcdefgPiHKAL entry
  2. ^abcShulgin AT (2003)."Basic Pharmacology and Effects". In Laing RR (ed.).Hallucinogens: A Forensic Drug Handbook. Forensic Drug Handbook Series. Elsevier Science. pp. 67–137.ISBN 978-0-12-433951-4. Archived fromthe original on 13 July 2025.
  3. ^abcdefKolaczynska KE, Luethi D, Trachsel D, Hoener MC, Liechti ME (2021)."Receptor Interaction Profiles of 4-Alkoxy-3,5-Dimethoxy-Phenethylamines (Mescaline Derivatives) and Related Amphetamines".Frontiers in Pharmacology.12 794254.doi:10.3389/fphar.2021.794254.PMC 8865417.PMID 35222010.
  4. ^abcHalberstadt AL, Chatha M, Klein AK, Wallach J, Brandt SD (May 2020)."Correlation between the potency of hallucinogens in the mouse head-twitch response assay and their behavioral and subjective effects in other species"(PDF).Neuropharmacology.167 107933.doi:10.1016/j.neuropharm.2019.107933.PMC 9191653.PMID 31917152.Table 4 Human potency data for selected hallucinogens. [...]
  5. ^abcTrachsel D, Lehmann D, Enzensperger C (2013).Phenethylamine: von der Struktur zur Funktion [Phenethylamines: From Structure to Function]. Nachtschatten-Science (in German) (1 ed.). Solothurn: Nachtschatten-Verlag. pp. 736–737, 741.ISBN 978-3-03788-700-4.OCLC 858805226.
  6. ^Nichols DE (1994)."Medicinal Chemistry and Structure–Activity Relationships". In Cho AK, Segal DS (eds.).Amphetamine and Its Analogs: Psychopharmacology, Toxicology, and Abuse. Academic Press. pp. 3–41.ISBN 978-0-12-173375-9.α-Methylation also seems to have less of an effect on potency in 3,4,5-substituted compounds, with perhaps a 2-fold increase of activity from mescaline to its amphetamine counterpart. Fewer examples are available in this substitution series, but the α-methyl congener of escaline (3,5-dimethoxy-4-ethoxyphenethylarnine) is virtually equipotent to escaline (Shulgin and Shulgin, 1991).
  7. ^abHalberstadt AL, Chatha M, Chapman SJ, Brandt SD (March 2019)."Comparison of the behavioral effects of mescaline analogs using the head twitch response in mice".Journal of Psychopharmacology.33 (3):406–414.doi:10.1177/0269881119826610.PMC 6848748.PMID 30789291.
  8. ^Benington F, Morin RD, Clarke LC (1954)."Synthesis of 4-Hydroxy- and 4-Ethoxy-3,5-dimethoxy-β-phenethylamines 1".Journal of the American Chemical Society.76 (21):5555–5556.Bibcode:1954JAChS..76.5555B.doi:10.1021/ja01650a084.ISSN 0002-7863. Retrieved18 October 2025.
  9. ^Braun U, Braun G, Jacob P, Nichols DE, Shulgin AT (1978)."Mescaline Analogs: Substitutions at the 4-Position"(PDF). In Barnett G, Trsic M, Willette RE (eds.).QuaSAR: Quantitative Structure Activity Relationships Of Analgesics, Narcotic Antagonists, And Hallucinogens(PDF). National Institute on Drug Abuse Research Monograph Series. Vol. 22. National Institute on Drug Abuse. pp. 27–37.PMID 101882.
  10. ^Shulgin AT."4-Ethoxy TMA / 4-Ethoxy-3,5-DMA / 3C-E"(PDF).PIHKAL notebooks transcripts, Part II. p. 222.
  11. ^"New drugs in Europe 2013".European Monitoring Centre for Drugs and Drug Addiction (EMCDDA). 2013.
  12. ^King LA (2014). "New phenethylamines in Europe".Drug Testing and Analysis.6 (7–8):808–818.doi:10.1002/dta.1570.PMID 24574327.

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