4-MeO-DMT

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4-MeO-DMT
4-MeO-DMT.png
Systematic (IUPAC) name
2-(4-Methoxy-1H-indol-3-yl)-N,N-dimethylethanamine
Identifiers
CAS Registry Number 3965-97-7 N
PubChem CID: 12017578
ChemSpider 23126449 YesY
ChEMBL CHEMBL32029 YesY
Chemical data
Formula C13H18N2O
Molecular mass 218.30 g·mol−1
 N (what is this?)  (verify)

4-MeO-DMT (4-methoxy-N,N-dimethyltryptamine) is a tryptamine derivative which has some central activity in animal tests similar to that of related psychedelic tryptamine drugs, although with significantly lower potency than either 5-MeO-DMT or 4-hydroxy-DMT (psilocin).[1][2][3][4]

See also[edit]

References[edit]

  1. ^ Glennon RA, Young R, Benington F, Morin RD (February 1982). "Hallucinogens as discriminative stimuli: a comparison of 4-OMe DMT and 5-OMe DMT with their methythio counterparts". Life Sciences 30 (5): 465–7. doi:10.1016/0024-3205(82)90463-5. PMID 6801410. 
  2. ^ Kline TB, Benington F, Morin RD, Beaton JM (August 1982). "Structure-activity relationships in potentially hallucinogenic N,N-dialkyltryptamines substituted in the benzene moiety". Journal of Medicinal Chemistry 25 (8): 908–13. doi:10.1021/jm00350a005. PMID 7120280. 
  3. ^ Kline TB, Benington F, Morin RD, Beaton JM, Glennon RA, Domelsmith LN, Houk KN, Rozeboom MD (November 1982). "Structure-activity relationships for hallucinogenic N,N-dialkyltryptamines: photoelectron spectra and serotonin receptor affinities of methylthio and methylenedioxy derivatives". Journal of Medicinal Chemistry 25 (11): 1381–3. doi:10.1021/jm00353a021. PMID 6815326. 
  4. ^ Nichols DE, Glennon RA. Medicinal Chemistry and Structure-Activity Relationships of Hallucinogens, in Hallucinogens, Neurochemical, Behavioral, and Clinical Perspectives (Raven Press 1984), pp 95-142. ISBN 978-0-89004-990-7