5-Ethyl-DMT

In the contemporary world, 5-Ethyl-DMT occupies a central place in our society. Its influence extends to all areas of life, from politics to popular culture, through technology and economics. This article will explore in depth the impact and relevance of 5-Ethyl-DMT, analyzing its implications and consequences for the world we live in. Through a multidisciplinary approach, we will seek to comprehensively understand this phenomenon and its ramifications, with the aim of providing a more complete and contextualized view of 5-Ethyl-DMT, in order to foster an enriching and constructive debate.

5-Ethyl-DMT
Identifiers
  • 2-(5-Ethyl-1H-indol-3-yl)-N,N-dimethylethanamine
CAS Number
PubChem CID
ChemSpider
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC14H20N2
Molar mass216.328 g·mol−1
3D model (JSmol)
  • CN(C)CCc1cc(ccc2CC)c1c2
  • InChI=1S/C14H20N2/c1-4-11-5-6-14-13(9-11)12(10-15-14)7-8-16(2)3/h5-6,9-10,15H,4,7-8H2,1-3H3 checkY
  • Key:ZEHXYLDGQMEYAX-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

5-Ethyl-N,N-dimethyltryptamine is a tryptamine derivative which acts as an agonist at the 5-HT1A and 5-HT1D serotonin receptors, with around 3x selectivity for 5-HT1D.

See also

References

  1. ^ Glennon RA, Hong SS, Bondarev M, Law H, Dukat M, Rakhi S, Power P, Fan E, Kinneau D, Kamboj R, Teitler M, Herrick-Davis K, Smith C (January 1996). "Binding of O-alkyl derivatives of serotonin at human 5-HT1D beta receptors". Journal of Medicinal Chemistry. 39 (1): 314–22. doi:10.1021/jm950498t. PMID 8568822.


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