Synthesis and Characterization of Psilocybin Metabolites and Deuterated Analogs

To support ongoing clinical trials, the major human metabolites of psilocybin were synthesized on a preparative scale, specifically psilocin-O-glucuronide and 4-hydroxyindole-3-acetic acid (4-HIAA), along with putative minor metabolites and several deuterium-labeled derivatives. Psilocybin, psilocin, psilocin-O-glucuronide, and 4-HIAA were assayed for engagement at seven serotonin receptor subtypes using a BRET-based binding assay, which showed that only psilocin exhibited any discernible binding across the subtypes investigated. Given the high cost and challenging preparation of these compounds, our work offers a comprehensive guide for researchers to access these resources, advancing both basic and clinical research with psilocybin and its metabolites.

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Publication Details

Journal
ACS Chemical Neuroscience
Published
2026-03-03
DOI
https://doi.org/10.1021/acschemneuro.5c00879
Primary Topic
Psychedelics and Drug Studies
Type
article
Field-Weighted Citation Impact
0.00
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article

Synthesis and Characterization of Psilocybin Metabolites and Deuterated Analogs

Rachel Friedman Ohana, Alexander M. Sherwood, Ilia A. Guzei, James J. Cali et al.
ACS Chemical Neuroscience
Psychedelics and Drug Studies
article

Synthesis and Characterization of Psilocybin Metabolites and Deuterated Analogs

Rachel Friedman Ohana, Alexander M. Sherwood, Ilia A. Guzei, James J. Cali, Mike Valley, Elise K. Burkhartzmeyer, Michael T. Faley, Samuel E. Williamson
article en

Abstract

To support ongoing clinical trials, the major human metabolites of psilocybin were synthesized on a preparative scale, specifically psilocin-O-glucuronide and 4-hydroxyindole-3-acetic acid (4-HIAA), along with putative minor metabolites and several deuterium-labeled derivatives. Psilocybin, psilocin, psilocin-O-glucuronide, and 4-HIAA were assayed for engagement at seven serotonin receptor subtypes using a BRET-based binding assay, which showed that only psilocin exhibited any discernible binding across the subtypes investigated. Given the high cost and challenging preparation of these compounds, our work offers a comprehensive guide for researchers to access these resources, advancing both basic and clinical research with psilocybin and its metabolites.

ACS Chemical NeuroscienceVol. 17(6)
University of Wisconsin–Madison (US), MRC Laboratory of Molecular Biology (GB), Promega (United States) (US), Laboratory of Molecular Genetics (PL), Usona Institute (US)
Openalex Percentile: Top 41%
Psychedelics and Drug Studies
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Synthesis and Characterization of Psilocybin Metabolites and Deuterated Analogs — Rachel Friedman Ohana, Alexander M. Sherwood, et al. · ACS Chemical Neuroscience (2026) | TGRS Research Map | TGRS