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2C-T-21.5

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
2C-T-21.5
Clinical data
Other names4-(2,2-Difluoroethylthio)-2,5-dimethoxyphenethylamine; 2,5-Dimethoxy-4-(2,2-difluoroethylthio)phenethylamine
Routes of
administration
Oral[1]
Drug classSerotonin receptor modulator;Serotonin 5-HT2A receptor agonist;Serotonergic psychedelic;Hallucinogen
Pharmacokinetic data
Duration of action8–14 hours[1]
Identifiers
  • 2-[4-(3,3-difluoropropylsulfanyl)-2,5-dimethoxyphenyl]ethanamine
CAS Number
PubChemCID
Chemical and physical data
FormulaC12H17F2NO2S
Molar mass277.33 g·mol−1
3D model (JSmol)
  • COC1=CC(=C(C=C1CCN)OC)SCC(F)F
  • InChI=1S/C12H17F2NO2S/c1-16-9-6-11(18-7-12(13)14)10(17-2)5-8(9)3-4-15/h5-6,12H,3-4,7,15H2,1-2H3
  • Key:LVCSIKISADNGMR-UHFFFAOYSA-N

2C-T-21.5, also known as4-(2,2-difluoroethylthio)-2,5-dimethoxyphenethylamine, is a lesser-knownpsychedelic drug related to compounds such as2C-T-21 and2C-T-28. It was originally named byAlexander Shulgin and discussed in his bookPiHKAL,[2] but was not synthesised at that time. 2C-T-21.5 was ultimately synthesised and tested byDaniel Trachsel some years later. It has abinding affinity of 146 nM at5-HT2A and 55 nM at5-HT2C. It produces typicalpsychedelic effects, being slightly less potent but somewhat longer acting than2C-T-2 or 2C-T-21,[3][4][5] with an active dose of 12–30 mg, and a duration of action of 8–14 hours. Unlike 2C-T-21 it will not form the highly toxicfluoroacetate as a metabolite, instead producing the less toxicdifluoroacetic acid.[1][6]

See also

[edit]

References

[edit]
  1. ^abcTrachsel D, Lehmann D, Enzensperger C (2013).Phenethylamine: Von der Struktur zur Funktion. Nachtschatten Verlag AG. pp. 789–791.ISBN 978-3-03788-700-4.
  2. ^Alexander Shulgin. "2C-T-21".PiHKAL.
  3. ^Trachsel D (2012). "Fluorine in psychedelic phenethylamines".Drug Testing and Analysis.4 (7–8):577–590.doi:10.1002/dta.413.PMID 22374819.
  4. ^Luethi D, Trachsel D, Hoener MC, Liechti ME (May 2018)."Monoamine receptor interaction profiles of 4-thio-substituted phenethylamines (2C-T drugs)"(PDF).Neuropharmacology.134 (Pt A):141–148.doi:10.1016/j.neuropharm.2017.07.012.PMID 28720478.
  5. ^Halberstadt AL, Luethi D, Hoener MC, Trachsel D, Brandt SD, Liechti ME (January 2023)."Use of the head-twitch response to investigate the structure-activity relationships of 4-thio-substituted 2,5-dimethoxyphenylalkylamines".Psychopharmacology.240 (1):115–126.doi:10.1007/s00213-022-06279-2.PMC 9816194.PMID 36477925.
  6. ^WO 2023/156450, Nivorozhkin A, Hartsel JA, Canal CE, Salituro FG, Mueller TA, Greene BJ, Belser A, Avery KL, Reichelt AC, Varty GB, Palfreyman M, "Therapeutic phenethylamine compositions and methods of use.", published 24 August 2023, assigned to Cybin Irl Ltd. 

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