5-MeO-MET

Chemical compound From Wikipedia, the free encyclopedia

5-MeO-MET, also known as 5-methoxy-N-methyl-N-ethyltryptamine, is a serotonin receptor modulator, putative serotonergic psychedelic, and relatively rare designer drug of the tryptamine family related to psychedelic drugs like methylethyltryptamine (MET) and 5-MeO-DMT.[2][3][4][5][6]

Quick facts Clinical data, Other names ...
5-MeO-MET
Clinical data
Other names5-OMe-MET; 5-Methoxy-N-methyl-N-ethyltryptamine
Drug classSerotonin receptor modulator; Serotonin 5-HT2A receptor agonist; Serotonergic psychedelic; Hallucinogen
Pharmacokinetic data
Onset of actionUnknown[1]
Duration of actionUnknown[1]
Identifiers
  • N-ethyl-2-(5-methoxy-1H-indol-3-yl)-N-methylethan-1-amine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC14H20N2O
Molar mass232.327 g·mol−1
3D model (JSmol)
  • CCN(CCc1c[nH]c2c1cc(OC)cc2)C
  • InChI=1S/C14H20N2O/c1-4-16(2)8-7-11-10-15-14-6-5-12(17-3)9-13(11)14/h5-6,9-10,15H,4,7-8H2,1-3H3
  • Key:AVECDEWGCOLCPZ-UHFFFAOYSA-N
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Use and effects

5-MeO-MET was not included nor mentioned in Alexander Shulgin's book TiHKAL (Tryptamines I Have Known and Loved).[1] Relatedly, its properties, such as dose and duration, and its effects were not described.[1] However, Nervewing later described the effects of 5-MeO-MET in an interview with Hamilton Morris and elsewhere.[7] They described 5-MeO-MET as producing no interesting psychological effects, as feeling like they had purely physically poisoned themselves, as feeling terrible and miserable, and as causing specific symptoms including nausea, chills, muscle aches, and almost vomiting, among others.[7]

Interactions

Pharmacology

Pharmacodynamics

Early studies found 5-MeO-MET to be more potent in animal behavioral tests than 5-MeO-DMT.[3][8] Subsequent studies confirmed that 5-MeO-MET interacts with serotonin receptors similarly to other psychedelic tryptamines.[9][10] A more modern study found that 5-MeO-MET is a potent serotonin 5-HT1A receptor ligand and serotonin 5-HT2A receptor agonist and produces the head-twitch response, a behavioral proxy of psychedelics, in rodents.[2][11] Its activities were of similar potency as 5-MeO-DMT.[2]

Chemistry

Analogues

Analogues of 5-MeO-MET include methylethyltryptamine (MET), 4-HO-MET (metocin), 4-AcO-MET (metacetin), 4-PrO-MET, 5-HO-MET, bretisilocin (5-fluoro-MET), 7F-5-MeO-MET, 5-MeO-DMT, 5-MeO-DET, 5-MeO-MPT, 5-MeO-EPT, 5-MeO-MALT, and 5-MeO-MiPT, among others.

History

5-MeO-MET was first synthesized and limitedly studied in the 1960s.[3][8][9] The drug was first identified on the illicit market in June 2012 in Sweden.[12] It was made illegal in Norway in 2013.[13]

Society and culture

Canada

5-MeO-MET is not a controlled substance in Canada as of 2025.[14]

Sweden

5-MeO-MET is a controlled substance in Sweden.[15]

United States

5-MeO-MET is not an explicitly controlled substance in the United States.[16] However, it could be considered a controlled substance under the Federal Analogue Act if intended for human consumption.

See also

References

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