Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

3C-DFE

From Wikipedia, the free encyclopedia
Psychedelic drug
Pharmaceutical compound
3C-DFE
Clinical data
Other names3C-F2EM; 4-(2,2-Difluoroethoxy)-3,5-dimethoxyamphetamine; α-Methyldifluoroescaline; 3C-Difluoroescaline
Routes of
administration
Oral[1][2]
Drug classSerotonin receptor modulator;Serotonergic psychedelic;Hallucinogen
ATC code
  • None
Pharmacokinetic data
Duration of action~10 hours[1][2]
Identifiers
  • 1-[4-(2,2-difluoroethoxy)-3,5-dimethoxyphenyl]propan-2-amine
CAS Number
PubChemCID
ChemSpider
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H19F2NO3
Molar mass275.296 g·mol−1
3D model (JSmol)
Melting point171 to 172 °C (340 to 342 °F)
  • COc1cc(CC(N)C)cc(OC)c1OCC(F)F
  • InChI=1S/C13H19F2NO3/c1-8(16)4-9-5-10(17-2)13(11(6-9)18-3)19-7-12(14)15/h5-6,8,12H,4,7,16H2,1-3H3
  • Key:TYXHBMNQOVLYRX-UHFFFAOYSA-N

3C-DFE, also known as4-(2,2-difluoroethoxy)-3,5-dimethoxyamphetamine or asα-methyldifluoroescaline (3C-difluoroescaline), is a lesser-knownpsychedelic drug of thephenethylamine,amphetamine, and3C families, which is afluorinatedderivative of3C-E.[1][3][4][2] It was firstsynthesised byDaniel Trachsel in 2002,[4][3] and has been reported as showing similar psychedelic activity to related compounds, with an active dose of around 22 mgorally and aduration of approximately 10 hours.[1]: 736 

Despite its psychedelic activity, binding studiesin vitro showed 3C-DFE to have a surprisingly weakbinding affinity of 2,695 nM at theserotonin5-HT2A receptor with negligible affinity at the serotonin5-HT2C receptor, making it only slightly higher affinity thanmescaline, despite its much higherpotencyin vivo.[1]: 737  However, thepharmacology of 3C-DFE was subsequently further studied and it was found to be a potent agonist of the serotonin 5-HT2A receptor, with anEC50Tooltip half-maximal effective concentration of 120 nM (83-fold that of mescaline in the same study) and anEmaxTooltip maximal efficacy of 95% (relative to 56% with mescaline in the study).[2]

See also

[edit]

References

[edit]
  1. ^abcdeTrachsel D, Lehmann D, Enzensperger C (2013).Phenethylamine Von der Struktur zur Funktion. Nachtschatten Verlag AG. pp. 704–723.ISBN 978-3-03788-700-4.
  2. ^abcdKolaczynska 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".Front Pharmacol.12 794254.doi:10.3389/fphar.2021.794254.PMC 8865417.PMID 35222010.
  3. ^abTrachsel, Daniel (2012). "Fluorine in psychedelic phenethylamines".Drug Testing and Analysis.4 (7–8):577–90.doi:10.1002/dta.413.PMID 22374819.
  4. ^abTrachsel, Daniel (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.

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
Others
Natural sources
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
Retrieved from "https://en.wikipedia.org/w/index.php?title=3C-DFE&oldid=1321573805"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp