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Fluoroescaline

From Wikipedia, the free encyclopedia

Pharmaceutical compound
Fluoroescaline
Clinical data
Other namesFE; 2-Fluoroescaline; 2-FE; FEM; 4-(2-Fluoroethoxy)-3,5-dimethoxyphenethylamine; 3,5-Dimethoxy-4-(2-fluoroethoxy)phenethylamine
Routes of
administration
Oral[1][2][3]
Drug classSerotonin receptor modulator;Serotonin5-HT2A receptoragonist;Serotonergic psychedelic;Hallucinogen
ATC code
  • None
Pharmacokinetic data
Duration of action~6 hours[1][2][3]
Identifiers
  • 2-[4-(2-fluoroethoxy)-3,5-dimethoxyphenyl]ethanamine
PubChemCID
ChemSpider
Chemical and physical data
FormulaC12H18FNO3
Molar mass243.278 g·mol−1
3D model (JSmol)
  • COC1=CC(=CC(=C1OCCF)OC)CCN
  • InChI=1S/C12H18FNO3/c1-15-10-7-9(3-5-14)8-11(16-2)12(10)17-6-4-13/h7-8H,3-6,14H2,1-2H3
  • Key:RODJFRFKJSPAGG-UHFFFAOYSA-N

Fluoroescaline (FE), also known as4-(2-fluoroethoxy)-3,5-dimethoxyphenethylamine, is apsychedelic drug of thephenethylamine andscaline families related tomescaline.[1][2][3] It is afluorinatedderivative ofescaline.[1][2][3] The drug is active at a dose of 75 mg or moreorally and itsduration is approximately 6 hours.[1][2][3] The drug has not been fully tested and it produced only weakhallucinogenic effects and noclosed-eye oropen-eye visuals at dose of 75 mg.[1] Fluoroescaline is notably lesspotent than escaline.[1][2][3] It is a low-potency near-full agonist of theserotonin5-HT2A receptor and also interacts with otherserotonin receptors andtargets.[3] Thechemical synthesis of fluoroescaline has been described. Fluoroescaline was first described in thescientific literature byDaniel Trachsel in 2002.[1][2][3][4] Itspharmacology was subsequently described in further detail in 2021.[3] It is not acontrolled substance inCanada as of 2025.[5]

See also

[edit]

References

[edit]
  1. ^abcdefghTrachsel 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. 706,710–711,716–717,736–737.ISBN 978-3-03788-700-4.OCLC 858805226.
  2. ^abcdefgTrachsel D (2012). "Fluorine in psychedelic phenethylamines".Drug Testing and Analysis.4 (7–8):577–590.doi:10.1002/dta.413.PMID 22374819.
  3. ^abcdefghiKolaczynska 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. ^Trachsel D (2002). "Synthese von neuen (Phenylalkyl)aminen zur Untersuchung von Struktur-Aktivitätsbeziehungen, Mitteilung 1, Mescalin Derivate".Helvetica Chimica Acta.85 (9):3019–3026.doi:10.1002/1522-2675(200209)85:9<3019::AID-HLCA3019>3.0.CO;2-4.
  5. ^"Controlled Drugs and Substances Act".Department of Justice Canada. Retrieved19 January 2026.

External links

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