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DOTFM

From Wikipedia, the free encyclopedia
(Redirected from2,5-Dimethoxy-4-trifluoromethylamphetamine)
Psychedelic drug
For the internet domain, see.fm.

Pharmaceutical compound
DOTFM
Clinical data
Other names2,5-Dimethoxy-4-trifluoromethylamphetamine; 4-Trifluoromethyl-2,5-dimethoxyamphetamine; DOTFM; 3C-TFM
Routes of
administration
Oral[1][2]
Legal status
Legal status
Pharmacokinetic data
Duration of actionUnknown[1][2]
Identifiers
  • (RS)-1-[2,5-Dimethoxy-4-(trifluoromethyl)phenyl]propan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC12H16F3NO2
Molar mass263.260 g·mol−1
3D model (JSmol)
  • FC(F)(F)c1cc(OC)c(cc1OC)CC(N)C
  • InChI=1S/C12H16F3NO2/c1-7(16)4-8-5-11(18-3)9(12(13,14)15)6-10(8)17-2/h5-7H,4,16H2,1-3H3 checkY
  • Key:WPGOTSORDNBMHP-UHFFFAOYSA-N checkY
  (verify)

2,5-Dimethoxy-4-trifluoromethylamphetamine (DOTFM) is apsychedelic drug of thephenethylamine,amphetamine, andDOx families.[3] It is theα-methylatedanalogue of2C-TFM. The drug is the mostpotent DOx psychedelic.[1][2]

Use and effects

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According toDaniel Trachsel, DOTFM is active as a psychedelic in humans at doses of 0.3 to 1 mg (300–1,000 μg) and itsduration is not listed.[1][2] It is the mostpotent psychedelic of the DOx family, followed byDOB (dose range 1–3 mg).[1][2]

Interactions

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See also:Psychedelic drug § Interactions, andTrip killer § Serotonergic psychedelic antidotes

Pharmacology

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Pharmacodynamics

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DOTFM acts as anagonist at theserotonin5-HT2A and5-HT2Creceptors.[3] Indrug discrimination tests in rats, DOTFM fully substituted forLSD and was slightly morepotent thanDOI.[3] In addition, (R)-DOTFM robustly induces thehead-twitch response, a behavioral proxy of psychedelic effects, in rodents, with equivalent potency as (R)-DOI.[4] The drug is around twice as potent as 2C-TFM inanimal studies.

In contrast to (R)-DOI, which has extraordinarily potent serotonin 5-HT2A receptor-mediatedanti-inflammatory effects,[5][6] DOTFM shows no anti-inflammatory effects.[7] The differences between the drugs in this regard appear to be due to differences infunctional selectivity at the serotonin 5-HT2A receptor.[7][4]

History

[edit]

DOTFM was firstsynthesized in 1994 by a team atPurdue University led byDavid E. Nichols.[3] The threshold dose in humans was reported byAlexander Shulgin in his 2011 bookThe Shulgin Index, Volume One: Psychedelic Phenethylamines and Related Compounds, who cited personal communication with an anonymous individual in 2003 as the source for the information.[8][1] Subsequently,Daniel Trachsel described a wider dose range in 2013, although did not report itsduration.[2]

See also

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References

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  1. ^abcdefTrachsel D (2012)."Fluorine in psychedelic phenethylamines".Drug Test Anal.4 (7–8):577–590.doi:10.1002/dta.413.PMID 22374819.The 4-trifluoromethyl derivative 2C-TFM (34) was identified as a potent 5-HT2A/C receptor agonist by Nichols et al. in 1994.[28] Together with its a-methyl congener DOTFM (35) it is among the most potent simple phenethylamines at these binding sites, showing comparable or slightly higher binding affinities than DOB (29) and DOI (30).[28] Compared to DOB (29) and DOI (30), both compounds 34 and 35 turned out to be of equal, or slightly increased potency in DD studies (rats, training drug: LSD).[28] Within the context of a DD study, this was the first time for a 2C derivative to be found equally potent to the potent 3C derivatives DOB (29) and DOI (30). In humans, initial experiments seem to be consistent with high potencies (34: 3–5 mg; 35: 0.3 mg or more. A.T. Shulgin, personal communication in 2003).[4]
  2. ^abcdefTrachsel 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.
  3. ^abcdNichols DE, Frescas S, Marona-Lewicka D, Huang X,Roth BL, Gudelsky GA, et al. (December 1994). "1-(2,5-Dimethoxy-4-(trifluoromethyl)phenyl)-2-aminopropane: a potent serotonin 5-HT2A/2C agonist".Journal of Medicinal Chemistry.37 (25):4346–4351.doi:10.1021/jm00051a011.PMID 7996545.
  4. ^abFlanagan TW, Foster TP, Galbato TE, Lum PY, Louie B, Song G, et al. (February 2024)."Serotonin-2 Receptor Agonists Produce Anti-inflammatory Effects through Functionally Selective Mechanisms That Involve the Suppression of Disease-Induced Arginase 1 Expression".ACS Pharmacology & Translational Science.7 (2):478–492.doi:10.1021/acsptsci.3c00297.PMC 10863441.PMID 38357283.The effects of (R)-DOTFM were examined in the head-twitch response (HTR) assay. (R)-DOTFM produced a strong HTR with a potent ED 50 of 0.60 μmol/kg. These values are equivalent to (R)-DOI, as previously determined.
  5. ^Nichols DE, Johnson MW, Nichols CD (February 2017). "Psychedelics as Medicines: An Emerging New Paradigm".Clinical Pharmacology and Therapeutics.101 (2):209–219.doi:10.1002/cpt.557.PMID 28019026.
  6. ^Yu B, Becnel J, Zerfaoui M, Rohatgi R, Boulares AH, Nichols CD (November 2008). "Serotonin 5-hydroxytryptamine(2A) receptor activation suppresses tumor necrosis factor-alpha-induced inflammation with extraordinary potency".The Journal of Pharmacology and Experimental Therapeutics.327 (2):316–323.doi:10.1124/jpet.108.143461.PMID 18708586.
  7. ^abFlanagan TW, Billac G, Nichols CD (2022)."Differential Regulation of Inflammatory Responses Following 5-HT 2 Receptor Activation in Pulmonary Tissues".The FASEB Journal.36 (S1) fasebj.2022.36.S1.R2617.doi:10.1096/fasebj.2022.36.S1.R2617.ISSN 0892-6638.
  8. ^Shulgin 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.Threshold oral activity [of DOTFM] reported in humans at 300 µg (Anon., 2003).

External links

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