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4C-TFM

From Wikipedia, the free encyclopedia

Pharmaceutical compound
4C-TFM
Clinical data
Other namesTFM-Ariadne; 4C-DOTFM; 4-Trifluoromethyl-2,5-dimethoxy-α-ethylphenethylamine; 2,5-Dimethoxy-4-trifluoromethyl-α-ethylphenethylamine
Drug classSerotonin5-HT2 receptoragonist;Serotonin 5-HT2A receptor agonist
ATC code
  • None
Identifiers
  • 1-[2,5-dimethoxy-4-(trifluoromethyl)phenyl]butan-2-amine
PubChemCID
Chemical and physical data
FormulaC13H18F3NO2
Molar mass277.287 g·mol−1
3D model (JSmol)
  • CCC(CC1=CC(=C(C=C1OC)C(F)(F)F)OC)N
  • InChI=1S/C13H18F3NO2/c1-4-9(17)5-8-6-12(19-3)10(13(14,15)16)7-11(8)18-2/h6-7,9H,4-5,17H2,1-3H3
  • Key:KJEMUKCPDLOVTI-UHFFFAOYSA-N

4C-TFM, also known asTFM-Ariadne or4C-DOTFM, as well as4-trifluoromethyl-2,5-dimethoxy-α-ethylphenethylamine, is aserotonin5-HT2 receptoragonist of thephenethylamine,phenylisobutylamine, and4C families related toAriadne (4C-D).[1][2] It is a closeanalogue of thepsychedelic drugs2C-TFM andDOTFM, with 2C-TFM having nosubstitution at theα carbon, DOTFM having an α-methyl group, and 4C-TFM having an α-ethyl group.[2][3] The drug is apotentagonist of the serotonin5-HT2A,5-HT2B, and5-HT2C receptors.[2] It shows similarefficacy as an agonist of these receptors as Ariadne, but shows about 6.4-fold higher potency as a serotonin 5-HT2A receptor agonist in comparison.[2] Like Ariadne, 4C-TFM produces an attenuatedhead-twitch response relative to the psychedelic drugDOPR, with a similar maximal response as Ariadne.[2] Thechemical synthesis of 4C-TFM has been described.[2] 4C-TFM was first described in thescientific literature by Michael Cunningham and colleagues in 2023.[2]

See also

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References

[edit]
  1. ^Duan W, Cao D, Wang S, Cheng J (January 2024). "Serotonin 2A Receptor (5-HT2AR) Agonists: Psychedelics and Non-Hallucinogenic Analogues as Emerging Antidepressants".Chemical Reviews.124 (1):124–163.doi:10.1021/acs.chemrev.3c00375.PMID 38033123.Ariadne (95) is a nonhallucinogenic 5-HT2AR agonist in the phenylalkylamine class of compounds,173 and its structure differs from that of DOM (91) by only an additional methyl group (Figure 11). A very recent SAR study by Cunningham et al. around ariadne showed that replacement of the 4-methyl group with a trifluoromethyl (96, 4C-TFM, EC50 = 28.6 nM, Emax = 79.9%) or an n-propyl (97, 4C-Pr, EC50 = 29.5 nM, Emax = 83.8%) led to good agonist potency at the 5-HT2AR in the Gq-dissociation BRET assay, while the cycolopropyl (98, 4CcycPr, EC50 = 153 nM, Emax = 75%) and MOM (99, 4C-MOM, EC50 = 441 nM, Emax = 77.8%) substitutions decreased compound potency.173 Ariadne showed lower signaling potency and efficacy compared to that of DOM in multiple signaling pathways examined, and it exhibited markedly more attenuated HTR effects than its hallucinogenic analogues.173
  2. ^abcdefgCunningham 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.
  3. ^Trachsel D, Lehmann D, Enzensperger C (2013).Phenethylamine: von der Struktur zur Funktion [Phenethylamines: From Structure to Function]. Nachtschatten-Science (in German) (1 ed.). Solothurn: Nachtschatten-Verlag.ISBN 978-3-03788-700-4.OCLC 858805226. Archived fromthe original on 21 August 2025.

External links

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