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2C-T-27

From Wikipedia, the free encyclopedia
Pharmaceutical compound
2C-T-27
Clinical data
Other names4-Benzylthio-2,5-dimethoxyphenethylamine
Drug classSerotonin receptor agonist;Serotonin5-HT2A receptoragonist;Serotonergic psychedelic;Hallucinogen
Identifiers
  • 2-(4-benzylsulfanyl-2,5-dimethoxyphenyl)ethanamine
PubChemCID
Chemical and physical data
FormulaC17H21NO2S
Molar mass303.42 g·mol−1
3D model (JSmol)
  • COC1=CC(=C(C=C1CCN)OC)SCC2=CC=CC=C2
  • InChI=1S/C17H21NO2S/c1-19-15-11-17(16(20-2)10-14(15)8-9-18)21-12-13-6-4-3-5-7-13/h3-7,10-11H,8-9,12,18H2,1-2H3
  • Key:GRZVJRPTNCONNT-UHFFFAOYSA-N

2C-T-27, also known as4-benzylthio-2,5-dimethoxyphenethylamine, is aserotonin5-HT2A receptoragonist andserotonergic psychedelic of thephenethylamine and2C families.[1][2][3][4] It was firstsynthesized and described byDaniel Trachsel in 2003.[2][3]

In addition to the serotonin 5-HT2A receptor, 2C-T-27 interacts with the serotonin5-HT2C receptor.[4] It showed higheraffinity for the serotonin 5-HT2A receptor than any other 2C drug (Ki = 1.6 nM), but itsactivationalpotency andefficacy were among the lowest (EC50Tooltip half-maximal effective concentration = 26 nM;EmaxTooltip maximal efficacy = 27%).[5][4]

The drug produces thehead-twitch response (HTR), a behavioral proxy of psychedelic effects, in rodents.[5] However, the HTR induced by 2C-T-27 is relatively weak.[1]

2C-T-27 has been reported to producehallucinogenic effects in humans.[1] Its dosage was reported by Trachsel to be 80 mg or moreorally and noduration was listed.[1]

See also

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References

[edit]
  1. ^abcdTrachsel D, Lehmann D, Enzensperger C (2013).Phenethylamine: von der Struktur zur Funktion [Phenethylamines: From Structure to Function]. Nachtschatten-Science (in German). Solothurn: Nachtschatten-Verlag. pp. 789–795.ISBN 978-3-03788-700-4.OCLC 858805226. Retrieved29 January 2025.
  2. ^abTrachsel D (2003). "Synthese von neuen (Phenylalkyl)aminen zur Untersuchung von Struktur–Aktivitätsbeziehungen. Mitteilung 2: 4-Thio-substituierte [2-(2,5-Dimethoxyphenyl)ethyl]amine (=2,5-Dimethoxybenzolethanamine)" [Synthesis of Novel (Phenylalkyl)amines for the Investigation of Structure–Activity Relationships. Part 2). 4-Thio-Substituted [2-(2,5-Dimethoxyphenyl)ethyl]amines (=2,5-Dimethoxybenzeneethanamines)].Helvetica Chimica Acta.86 (7):2610–2619.doi:10.1002/hlca.200390210.ISSN 0018-019X.
  3. ^abMeyers-Riggs B (3 April 2011)."Shulgin's Sulfur Symphony".countyourculture. Retrieved17 February 2025.2C-T-27 (2,5-dimethoxy-4-benzylthiophenethylamine ) Synthesized by Daniel Trachsel but has not been bioassayed to public knowledge. [...] Trachsel, D. Synthesis of novel (phenylalkyl)amines for the investigation of structure-activity relationships. Part 2. 4-Thio-substituted [2-(2,5-dimethoxyphenyl)ethyl]amines (=2,5-dimethoxybenzeneethanamines). Helv. Chim. Acta, 5 Aug 2003, 86 (7), 2610–2619.
  4. ^abcLuethi D, Trachsel D, Hoener MC, Liechti ME (May 2018)."Monoamine receptor interaction profiles of 4-thio-substituted phenethylamines (2C-T drugs)".Neuropharmacology.134 (Pt A):141–148.doi:10.1016/j.neuropharm.2017.07.012.PMID 28720478.
  5. ^abHalberstadt 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"(PDF).Psychopharmacology (Berl).240 (1):115–126.doi:10.1007/s00213-022-06279-2.PMC 9816194.PMID 36477925.

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