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2C-T-3

From Wikipedia, the free encyclopedia
Pharmaceutical compound
2C-T-3
Clinical data
Other names2C-T-20; 4-Methallylthio-2,5-dimethoxyphenethylamine
Routes of
administration
Oral[1]
Drug classSerotonin receptor modulator;Serotonin 5-HT2A receptor agonist;Serotonergic psychedelic;Hallucinogen
ATC code
  • None
Pharmacokinetic data
Duration of action8–14 hours[1]
Identifiers
  • 2-{2,5-dimethoxy-4-[(2-methylprop-2-en-1-yl)sulfanyl]phenyl}ethan-1-amine
CAS Number
PubChemCID
ChemSpider
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC14H21NO2S
Molar mass267.39 g·mol−1
3D model (JSmol)
  • CC(=C)CSC1=C(C=C(C(=C1)OC)CCN)OC
  • InChI=1S/C14H21NO2S/c1-10(2)9-18-14-8-12(16-3)11(5-6-15)7-13(14)17-4/h7-8H,1,5-6,9,15H2,2-4H3
  • Key:JCDUUDQZKIXJJP-UHFFFAOYSA-N

2C-T-3, also initially numbered as2C-T-20 and also known as4-methallylthio-2,5-dimethoxyphenethylamine, is a lesser-knownpsychedelic drug related to compounds such as2C-T-7 and2C-T-16. It was named byAlexander Shulgin but was never made or tested by him, and was instead first synthesised byDaniel Trachsel some years later. It has abinding affinity of 11nM at5-HT2A and 40nM at5-HT2C. It is reportedly a potent psychedelic drug with an active dose in the 15–40 mg range, and a duration of action of 8–14 hours, with visual effects comparable to related drugs such asmethallylescaline.[2][3][1]

See also

[edit]

References

[edit]
  1. ^abcTrachsel D, Lehmann D, Enzensperger C (2013).Phenethylamine: Von der Struktur zur Funktion. Nachtschatten Verlag AG. pp. 788–794.ISBN 978-3-03788-700-4.
  2. ^Trachsel D (2003). "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.
  3. ^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.S2CID 7135811.

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