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4-MeO-DMT

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
4-MeO-DMT
Identifiers
  • 2-(4-Methoxy-1H-indol-3-yl)-N,N-dimethylethanamine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H18N2O
Molar mass218.300 g·mol−1
3D model (JSmol)
  • CN(C)CCC1=CNC2=CC=CC(OC)=C21
  • InChI=1S/C13H18N2O/c1-15(2)8-7-10-9-14-11-5-4-6-12(16-3)13(10)11/h4-6,9,14H,7-8H2,1-3H3 checkY
  • Key:HFYHBTWTJDAYGW-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

4-MeO-DMT (4-methoxy-N,N-dimethyltryptamine) is atryptaminederivative which has somecentral activity in animal tests similar to that of relatedpsychedelictryptamine drugs, although with significantly lower potency than either5-MeO-DMT or4-hydroxy-DMT (psilocin).[1][2][3][4]

Legality

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In the United States 4-MeO-DMT is a Schedule 1 controlled substance as a positional isomer of5-MeO-DMT.[5]

See also

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References

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  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 (1984)."Medicinal Chemistry and Structure-Activity Relationships of Hallucinogens". In Jacobs BL (ed.).Hallucinogens: Neurochemical, Behavioral, and Clinical Perspectives. New York: Raven Press. pp. 95–142.ISBN 978-0-89004-990-7.OCLC 10324237.
  5. ^"Lists of Scheduling Actions Controlled Substances Regulated Chemical"(PDF).deadiversion.usdoj.gov. Retrieved8 April 2023.
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
Triptans
Cyclized tryptamines
Isotryptamines
Related compounds
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