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

Lindsay P. Cameron, David E. Olson

ACS Chemical Neuroscience July 23, 2018 DOI: 10.1021/acschemneuro.8b00101 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Review Peer reviewed
Topics 5-MeO-DMT DMT
Keywords Hallucinogen
Citations 114
Key findings DMT is the archetype for all indole-containing serotonergic psychedelics, is ubiquitous in nature, and remains an underappreciated molecule in psychedelic science.

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.