4C-T-2

In today's world, 4C-T-2 is a topic that has gained great importance and relevance in all areas of daily life. From the personal, through the professional, to the social sphere, 4C-T-2 has become a point of interest and constant debate. Its impact has been notably perceived in various aspects, generating conflicting opinions, theories and research that seek to fully understand its influence on current society. In this article, we are going to address the different aspects of 4C-T-2, exploring its meaning, implications and possible paths for its future development.
4C-T-2
Clinical data
ATC code
  • none
Legal status
Legal status
  • In general: uncontrolled
Identifiers
  • 1-butan-2-amine
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC14H23NO2S
Molar mass269.40 g·mol−1
3D model (JSmol)
  • COC1=C(CC(CC)N)C=C(OC)C(SCC)=C1
  • InChI=1S/C14H23NO2S/c1-5-11(15)7-10-8-13(17-4)14(18-6-2)9-12(10)16-3/h8-9,11H,5-7,15H2,1-4H3 checkY
  • Key:KLAWPCIXPDTGCZ-UHFFFAOYSA-N checkY
  (verify)

2,5-Dimethoxy-4-ethylthio-α-ethylphenethylamine (4C-T-2) is a synthetic drug of the phenethylamine chemical class. It is the α-ethylated analogue of 2C-T-2.

Pharmacology

Binding profile

4C-T-2 has affinity (Ki) for the 5-HT1A (5,339 nM), 5-HT1E (9,879 nM), 5-HT2A (274.1 nM), 5-HT2B (58.1 nM), 5-HT2C (468.6 nM), 5-HT5A (1,587 nM), 5-HT7 (3,829), D3 (1,273 nM), β2-adrenergic (124.9 nM), I1 (946.5 nM), and σ1 (514 nM) receptors.[1] The activity of 4C-T-2 at these sites has not been assayed, with the exception of the 5-HT2A and 5-HT2C receptors where it acts as a partial agonist.[1]

See also

References

  1. ^ a b Ray TS (February 2010). "Psychedelics and the human receptorome". PLOS ONE. 5 (2): e9019. Bibcode:2010PLoSO...5.9019R. doi:10.1371/journal.pone.0009019. PMC 2814854. PMID 20126400.
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