Skip to content

Natural Product Communications

ISSN 1555-9475

3 papers in the library · 16 citations · publishing 2012-2026

Papers

Alkaloids of the Cactaceae — The Classics

Natural Product Communications April 20, 2026 Bruce K. Cassels 11 citations

Cactus alkaloids have been studied for 120 years. Early work identified classic compounds; later research isolated many similar analogs. Synthesis is straightforward, but biosynthesis, especially of isoquinoline alkaloids, remains poorly understood. Mescaline's pharmacology has been studied extensively due to its striking effects, while hordenine and tetrahydroisoquinoline alkaloids have received less attention and are often considered inactive. However, some recorded activities of tetrahydroisoquinolines suggest a need for further study, particularly regarding their co-administration with mescaline in dried cacti and cactus beverages.

Concise Synthesis of N,N -Dimethyltryptamine and 5-Methoxy- N,N -dimethyltryptamine Starting with Bufotenine from Brazilian Anadenanthera ssp

Natural Product Communications April 1, 2015 Leandro A. Moreira, Maria M. Murta, Claudia C. Gatto et al. 3 citations

Bufotenine, a compound found in seeds of the Anadenanthera tree native to the Brazilian cerrado, was extracted using an acid-base method. The researchers developed a new, short process to convert bufotenine into N,N-dimethyltryptamine and 5-methoxy-N,N-dimethyltryptamine, involving a novel bufotenine-aminoborane complex. They also established a straightforward method to produce 5-hydroxy-N,N,N-trimethyltryptamine from bufotenine. This work presents bufotenine as a source for producing N,N-dimethyltryptamines for pharmacological, toxicological, or synthetic use.

Quantitative Analysis of Substituted N,N-Dimethyl-tryptamines in the Presence of Natural Type XII Alkaloids

Natural Product Communications October 1, 2012 Bojidarka Ivanova, Michael Spiteller 2 citations

A validated analytical protocol using electronic absorption spectroscopy achieves a limit of detection of 7.2 × 10⁻⁷ mol/L and a limit of quantification of 24 × 10⁻⁷ mol/L for mixtures of hallucinogens including N,N-dimethyltryptamine (DMT) and its derivatives in the presence of β-carbolines. Additional protocols using HPLC, ESI-MS, MS/MS, MALDI-MS, and Raman spectroscopy are partially validated. The known synergistic effect that increases psychoactive properties and reported acute poisoning cases from these compounds underscore the need for such precise analytical methods, which are relevant to criminal forensic analysis.