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dimethyltryptamine

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(n,n-dimethyltryptamine szócikkből átirányítva)
Dimethyltryptamine
Clinical data
Other namesDimethyltryptamine; DMT; N,N-DMT
Routes of
administration
By mouth (usually with an MAOITooltip monoamine oxidase inhibitor), inhalation, insufflation, rectal, intramuscular, intravenous
Drug classSerotonergic psychedelic (hallucinogen)
ATC code
  • None
Physiological data
Source tissuesCentral nervous system (exact source tissues are not fully established)
Target tissuesCentral nervous system
ReceptorsAt least 13 receptors (e.g., serotonin, sigma, trace amine-associated)
PrecursorTryptophan
MetabolismOxidative deamination (MAO-ATooltip Monoamine oxidase A), N-oxidation, N-demethylation, peroxidation
Legal status
Legal status
Pharmacokinetic data
BioavailabilityVery low and inactive (except with an MAOITooltip monoamine oxidase inhibitor)
MetabolismOxidative deamination (MAO-ATooltip Monoamine oxidase A), N-oxidation, N-demethylation, peroxidation
Metabolites
Onset of action
Elimination half-life
  • Alone: 5–15 min
  • With an MAOITooltip monoamine oxidase inhibitor: 1–4 hours
Duration of action
ExcretionUrine
Identifiers
  • 2-(1H-Indol-3-yl)-N,N-dimethylethanamine
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
PDB ligand
Chemical and physical data
FormulaC12H16N2
Molar mass188.274 g·mol−1
3D model (JSmol)
Density1.099 g/cm3
Melting point40 °C (104 °F)
Boiling point160 °C (320 °F) at 0.6 Torr (80 Pa)

also reported as

80–135 °C (176–275 °F) at 0.03 Torr (4.0 Pa)
  • CN(CCC1=CNC2=C1C=CC=C2)C
  • InChI=1S/C12H16N2/c1-14(2)8-7-10-9-13-12-6-4-3-5-11(10)12/h3-6,9,13H,7-8H2,1-2H3 checkY
  • Key:DMULVCHRPCFFGV-UHFFFAOYSA-N checkY
  (verify)


Főnév

dimethyltryptamine (tsz. dimethyltryptamines)

  1. (gyógyszertan) dimetiltriptamin