5-MeS-DMT

Source: Wikipedia, the free encyclopedia.
5-MeS-DMT
Names
Preferred IUPAC name
N,N-Dimethyl-2-[5-(methylsulfanyl)-1H-indol-3-yl]ethan-1-amine
Other names
5-Methylthio-N,N-dimethyltryptamine
Identifiers
3D model (
JSmol
)
ChEMBL
ChemSpider
UNII
  • InChI=1S/C13H18N2S/c1-15(2)7-6-10-9-14-13-5-4-11(16-3)8-12(10)13/h4-5,8-9,14H,6-7H2,1-3H3 checkY
    Key: YOGJZQGRTVMCPY-UHFFFAOYSA-N checkY
  • InChI=1/C13H18N2S/c1-15(2)7-6-10-9-14-13-5-4-11(16-3)8-12(10)13/h4-5,8-9,14H,6-7H2,1-3H3
    Key: YOGJZQGRTVMCPY-UHFFFAOYAL
  • CN(CCC1=CNC2=C1C=C(SC)C=C2)C
Properties
C13H18N2S
Molar mass 234.36 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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5-MeS-DMT (5-methylthio-N,N-dimethyltryptamine) is a lesser-known

mg.[1]
The duration listed as very short (less than one hour), just like DMT. 5-MeS-DMT produces similar effects to DMT, but weaker. Shulgin describes his feelings while on a low dose of this drug as "pointlessly stoned", although at a higher dose of 20 mg he says it is "quite intense" and suggests that a higher dose still might have full activity.

5-MeS-DMT has been the subject of only limited clinical testing, with several small behavioral studies in rats indicating that it is a less potent than 5-MeO-DMT or 4-hydroxy-DMT (psilocin) but more effective than either 4-MeO-DMT or 4-MeS-DMT.[2][3][4]

See also

  • Tryptamine
  • Psychedelics, dissociatives and deliriants

References