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4C (psychedelics)

From Wikipedia, the free encyclopedia
Class of chemical compounds
Ariadne (4C-D).

4C (4C-x), also known as4-substituted 2,5-dimethoxy-α-ethylphenethylamines, is a general name for the family ofpsychedelic and relatedphenylisobutylamines (α-ethylphenethylamines) havingmethoxy groups at the 2 and 5positions of thephenylring and a 4-positionsubstituent.[1][2][3][4] Thesecompounds areanalogues of the2Cs andDOx drugs, but the α-alkylchain has been further lengthed (0 carbons for 2C, 1 carbon for DOx, and 2 carbons for 4C).[1][2][3]

The most notable and well-known of the 4C drugs isAriadne (4C-D).[1][2][3] This drug produces only threshold psychedelic effects and has been described as non-hallucinogenic or as having "the alert of a psychedelic, with none of the rest of the package".[2] These unique properties have made Ariadne of interest for potential therapeutic applications.[2] In contrast to Ariadne, other 4C drugs, such as4C-B, have been reported to be more significantly psychedelic.[3] Thepharmacology of the 4C drugs has been studied and they are known to act asserotonin5-HT2A receptoragonists, but with lowerefficacy than other related psychedelics like the 2Cs and DOx drugs.[4]

4C drugs have been developed and/or studied byAlexander Shulgin,[1][2]Daniel Trachsel,[3] and Michael Cunningham and colleagues.[4]

List of 4C drugs

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StructureName(s)Chemical nameCAS #
Ariadne (4C-D)1-(2,5-Dimethoxy-4-methylphenyl)butan-2-amine52842-59-8
4C-B1-(2,5-Dimethoxy-4-bromophenyl)butan-2-amine69294-23-1
4C-C1-(2,5-Dimethoxy-4-chlorophenyl)butan-2-amine791010-74-7
4C-E[5]1-(2,5-Dimethoxy-4-ethylphenyl)butan-2-amine?
4C-I1-(2,5-Dimethoxy-4-iodophenyl)butan-2-amine758631-75-3
4C-N1-(2,5-Dimethoxy-4-nitrophenyl)butan-2-amine775234-58-7
4C-P1-(2,5-Dimethoxy-4-(n-propyl)phenyl)butan-2-amine?
4C-T-21-[2,5-Dimethoxy-4-(ethylthio)phenyl]butan-2-amine850007-13-5

Various other 4C drugs have also been studied and described.[4]

See also

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References

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  1. ^abcdShulgin, A.; Manning, T.; Daley, P.F. (2011).The Shulgin Index, Volume One: Psychedelic Phenethylamines and Related Compounds. Vol. 1. Berkeley: Transform Press.ISBN 978-0-9630096-3-0. Retrieved2 November 2024.
  2. ^abcdefShulgin, Alexander;Shulgin, Ann (September 1991).PiHKAL: A Chemical Love Story.Berkeley, California:Transform Press.ISBN 0-9630096-0-5.OCLC 25627628.
  3. ^abcdeTrachsel, 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.ISBN 978-3-03788-700-4.OCLC 858805226. Retrieved31 January 2025.
  4. ^abcdCunningham MJ, Bock HA, Serrano IC, Bechand B, Vidyadhara DJ, Bonniwell EM, Lankri D, Duggan P, Nazarova AL, Cao AB, Calkins MM, Khirsariya P, Hwu C, Katritch V, Chandra SS, McCorvy JD, Sames D (January 2023)."Pharmacological Mechanism of the Non-hallucinogenic 5-HT2A Agonist Ariadne and Analogs".ACS Chemical Neuroscience.14 (1):119–135.doi:10.1021/acschemneuro.2c00597.PMC 10147382.PMID 36521179.
  5. ^Shulgin AT. Treatment of senile geriatric patients to restore performance. Patent US 4034113

External links

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