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Archiv der Pharmazie

ISSN 1521-4184

4 papers in the library · 20 citations · publishing 1976-2025

Papers

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Efficient Acyloxymethylation of Psilocin and Other Tryptamines Yielding ACOM Prodrugs for Psychedelic-Assisted Therapy.

Archiv der Pharmazie July 1, 2025 Judith Stirn, Christian D. Klein

Acyloxymethyl (ACOM) derivatives of tryptamines such as the psychedelic drug psilocin and the anti-migraine drug sumatriptan bear potential as prodrugs. Previous synthetic approaches suffer from insufficient chemoselectivity between the desired functionalization of the phenolic (psilocin) or sulfonamide (sumatriptan) groups versus other reactive groups in the parent drugs. We report a novel...

Xylazine as an emerging new psychoactive substance; focuses on both 5‐HT7 and κ‐opioid receptors' molecular interactions and isosteric replacement

Archiv der Pharmazie March 1, 2025 Giuseppe Floresta, Alberto Granzotto, Vincenzo Patamia et al. 12 citations

Abstract Xylazine, traditionally used as a veterinary sedative, has recently emerged as a new psychoactive substance, being typically ingested in combination with fentanyl derivatives and hence raising significant public health concerns. Despite its increasing prevalence, little is known about its molecular interactions with human neuroreceptors, specifically the serotonin 7 (5‐HT 7 R) and...

Synthesis of Baeocystin, a natural Psilocybin Analogue

Archiv der Pharmazie 1988 Rudolf Brenneisen, Stefan Borner, Nelly Peter‐oesch et al. 8 citations

Abstract Baeocystin ( 7 ) (4‐phosphoryloxy‐N‐methyltryptamine) has been synthesized starting from 2‐methyl‐3‐nitrophenol ( 1 ). The spectral data (UV, IR, 1 H‐, 31 P‐, 13 C‐NMR, MS) are identical with those of 7 isolated from Psilocybe semilanceata .

Polymorphe Modifikationen und Solvate von Psilocin und Psilocybin

Archiv der Pharmazie 1976 M. Kuhnert‐brandstätter, Wolfgang Heindl

Abstract Von Psilocin konnten drei polymorphe Modifikationen dargestellt werden, die sich durch ihr Verhalten beim Kristallisieren und Schmelzen sowie durch ihre IR‐Spektren unterscheiden. Mod. I schmilzt bei 170–173°, Mod. II bei 161°, Mod, III wird immer umgewandelt; ihr Schmp. konnte nicht bestimmt werden. Diese Form läßt sich dagegen durch ihr IR‐Spektrum sehr gut charakterisieren....