Dark Classics in Chemical Neuroscience: N, N-Dimethyltryptamine (DMT)

ACS Chem Neurosci. 2018 Oct 17;9(10):2344-2357. doi: 10.1021/acschemneuro.8b00101. Epub 2018 Jul 23.

Abstract

Though relatively obscure, N, N-dimethyltryptamine (DMT) is an important molecule in psychopharmacology as it is the archetype for all indole-containing serotonergic psychedelics. Its structure can be found embedded within those of better-known molecules such as lysergic acid diethylamide (LSD) and psilocybin. Unlike the latter two compounds, DMT is ubiquitous, being produced by a wide variety of plant and animal species. It is one of the principal psychoactive components of ayahuasca, a tisane made from various plant sources that has been used for centuries. Furthermore, DMT is one of the few psychedelic compounds produced endogenously by mammals, and its biological function in human physiology remains a mystery. In this review, we cover the synthesis of DMT as well as its pharmacology, metabolism, adverse effects, and potential use in medicine. Finally, we discuss the history of DMT in chemical neuroscience and why this underappreciated molecule is so important to the field of psychedelic science.

Keywords: DMT; N,N-Dimethyltryptamine; ayahuasca; hallucinogen; psychedelic.

Publication types

  • Historical Article
  • Review

MeSH terms

  • Animals
  • Banisteriopsis
  • Hallucinogens / history
  • Hallucinogens / metabolism
  • Hallucinogens / pharmacology*
  • Hallucinogens / therapeutic use
  • History, 20th Century
  • History, 21st Century
  • Humans
  • N,N-Dimethyltryptamine / history
  • N,N-Dimethyltryptamine / metabolism
  • N,N-Dimethyltryptamine / pharmacology*
  • N,N-Dimethyltryptamine / therapeutic use
  • Plant Preparations

Substances

  • Hallucinogens
  • Plant Preparations
  • N,N-Dimethyltryptamine