Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

DOYN

From Wikipedia, the free encyclopedia
(Redirected from2,5-Dimethoxy-4-ethynylamphetamine)

Pharmaceutical compound
DOYN
Clinical data
Other names4-Ethynyl-2,5-dimethoxyamphetamine; 2,5-Dimethoxy-4-ethynylamphetamine
Routes of
administration
Oral[1]
Drug classSerotonergic psychedelic;Hallucinogen
ATC code
  • None
Pharmacokinetic data
Duration of action10–15 hours[1]
Identifiers
  • 1-(4-ethynyl-2,5-dimethoxyphenyl)propan-2-amine
CAS Number
PubChemCID
Chemical and physical data
FormulaC13H17NO2
Molar mass219.284 g·mol−1
3D model (JSmol)
  • COc1cc(C#C)c(cc1CC(N)C)OC
  • InChI=1S/C13H17NO2/c1-5-10-7-13(16-4)11(6-9(2)14)8-12(10)15-3/h1,7-9H,6,14H2,2-4H3
  • Key:XSBAOBBZMYENRL-UHFFFAOYSA-N

DOYN, also known as4-ethynyl-2,5-dimethoxyamphetamine, is aserotonergic psychedelic of thephenethylamine,amphetamine, andDOx families.[1][2][3] According toDaniel Trachsel, it produceshallucinogenic effects with a dose range of 2 to 6 mg and aduration of 10 to 15 hours.[1] The drug's effects are described as typical psychedelic effects includingfantasy,imagery, andvisuals.[1] It is described as having a relatively short duration compared to 4-alkyl DOxderivatives likeDOM, perhaps due to more rapidmetabolism.[1] DOYN was first mentioned in thescientific literature by Trachsel in 2003 and was then described in more depth by him in 2013.[1][2][3] It is acontrolled substance inCanada under phenethylamine blanket-ban language.[4]

See also

[edit]

References

[edit]
  1. ^abcdefgTrachsel 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. 768, 778, 780, 810.ISBN 978-3-03788-700-4.OCLC 858805226.Als Alkinderivat existiert das DOYN (33) als einziger Vertreter. Die Synthese erfolgte in Analogie zu Ref. [411. Es zeigt typische psychedelische Wirkungen begleitet von Fantasy, Imagery und Visuals (Siche Kapitel 8.5.18 für Begriffserklärung) im Bereich von 2—6mg gepaart von einer Wirkdauer von 10—15h. Diese Wirkdauer ist — im Vergleich zu den 4-alkylierten Analoga — eher kurz. Es darf auf einen etwas rascheren Metabolismus (im Bereich der Dreifachbindung) im Vergleich zu DOET (14) spekuliert werden. Das als biphasisch beschriebene Wirkprofil deutet auf aktive Metaboliten hin.
  2. ^abShulgin A, Manning T, Daley PF (2011)."#60. DOM".The Shulgin Index, Volume One: Psychedelic Phenethylamines and Related Compounds. Vol. 1. Berkeley, CA: Transform Press. pp. 118–129.ISBN 978-0-9630096-3-0.OCLC 709667010.
  3. ^abTrachsel D (2003)."Synthesis of Novel (Phenylalkyl)amines for the Investigation of Structure–Activity Relationships, Part 3: 4-Ethynyl-2,5-dimethoxyphenethylamine (=4-Ethynyl-2,5-dimethoxybenzeneethanamine; 2C-YN)".Helvetica Chimica Acta.86 (8):2754–2759.doi:10.1002/hlca.200390224.ISSN 0018-019X. Retrieved21 June 2025.
  4. ^"Controlled Drugs and Substances Act".Department of Justice Canada. Retrieved19 January 2026.

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
Others
Natural sources
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


Stub icon

Thishallucinogen-related article is astub. You can help Wikipedia byadding missing information.

Retrieved from "https://en.wikipedia.org/w/index.php?title=DOYN&oldid=1333832674"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2026 Movatter.jp