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4C-T-2

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
4C-T-2
Clinical data
Other names4-Ethylthio-2,5-dimethoxy-α-ethylphenethylamine
ATC code
  • None
Legal status
Legal status
  • In general: uncontrolled
Identifiers
  • 1-[(2,5-dimethoxy-4-ethylthio)phenyl]butan-2-amine
CAS Number
PubChemCID
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)

4C-T-2, also known as2,5-dimethoxy-4-ethylthio-α-ethylphenethylamine, is asynthetic drug of thephenethylamine,phenylisobutylamine, and4C families.[1][2][3] It is theα-ethylatedanalogue of2C-T-2.[1][2][3]

Pharmacology

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Pharmacodynamics

[edit]
4C-T-2 activities
TargetAffinity (Ki, nM)
5-HT1A5,339
5-HT1B>10,000
5-HT1D>10,000
5-HT1E9,879
5-HT1FND
5-HT2A274 (Ki)
13.1–53 (EC50Tooltip half-maximal effective concentration)
78% (EmaxTooltip maximal efficacy)
5-HT2B58.1 (Ki)
630 (EC50)
ND (Emax)
5-HT2C469 (Ki)
7.3–13.2 (EC50)
86–121% (
Emax)
5-HT3>10,000
5-HT4ND
5-HT5A1,587
5-HT6>10,000
5-HT73,829
α1A,α1B>10,000
α1DND
α2Aα2C>10,000
β1>10,000
β2124.9
β3ND
D1,D2>10,000
D31,273
D4,D5>10,000
H1H4>10,000
M1M5>10,000
I1946.5
σ1514.6
σ2>10,000
TAAR1Tooltip Trace amine-associated receptor 1ND
SERTTooltip Serotonin transporter>10,000 (Ki)
NETTooltip Norepinephrine transporter>10,000 (Ki)
DATTooltip Dopamine transporter>10,000 (Ki)
MAO-ATooltip Monoamine oxidase A11,800 (IC50Tooltip half-maximal inhibitory concentration)
MAO-BTooltip Monoamine oxidase B>100,000 (IC50)
Notes: The smaller the value, the more avidly the drug binds to the site. All proteins are human unless otherwise specified.Refs:[4][5][2][3][6]

4C-T-2 acts as aserotonin5-HT2 receptoragonist, including of the serotonin5-HT2A,5-HT2B, and5-HT2C receptors.[2][3]

History

[edit]

4C-T-2 was first described in thescientific literature by at least 2005.[6] It was more fully characterized in 2010[2] and then in 2023.[3]

See also

[edit]

References

[edit]
  1. ^abShulgin A, Manning T, Daley P (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. ^abcdeRay 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.
  3. ^abcdeCunningham MJ, Bock HA, Serrano IC, Bechand B, Vidyadhara DJ, Bonniwell EM, et al. (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.Table S2. 5-HT2A and 5-HT2B IP1 agonism assay summary (EC50 values, duplicate averages only), performed at Cerep, Eurofins France [...]
  4. ^"Kᵢ Database".PDSP. 1 April 2025. Retrieved1 April 2025.
  5. ^Liu T."BindingDB BDBM50164331 1-(4-Ethylsulfanyl-2,5-dimethoxy-benzyl)-propylamine::CHEMBL372719".BindingDB. Retrieved1 April 2025.
  6. ^abGallardo-Godoy A, Fierro A, McLean TH, Castillo M, Cassels BK, Reyes-Parada M, et al. (April 2005)."Sulfur-substituted alpha-alkyl phenethylamines as selective and reversible MAO-A inhibitors: biological activities, CoMFA analysis, and active site modeling".Journal of Medicinal Chemistry.48 (7):2407–2419.doi:10.1021/jm0493109.PMID 15801832.

External links

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