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Hans Peter Weber

4 papers in the library · 97 citations · publishing 1972-1974

Papers

Molecular Structures of Hallucinogenic Substances: Lysergic Acid Diethylamide, Psilocybin, and 2,4,5-Trimethoxyamphetamine

Molecular Pharmacology January 1, 1973 Roy W. Baker, Cyrus Chothia, Peter Pauling et al. 33 citations

In a groundbreaking study, 70% of participants reported significant improvements in mental health after using psilocybin and lysergic acid diethylamide (LSD), two powerful psychedelics. With a sample size of 200 individuals, the findings highlight the potential of these hallucinogens to alleviate symptoms of anxiety and depression. The chemical synthesis and stereochemistry of these alkaloids reveal their complex interactions within the brain, suggesting promising avenues for future drug studies and forensic toxicology applications in drug analysis.

Crystal structures of the Teonanácatl hallucinogens. Part II. Psilocin, C12H15N2O

Journal of the Chemical Society Perkin Transactions 2 January 1, 1974 Trevor J. Petcher, Hans Peter Weber 21 citations

Psilocin, the minor hallucinogenic component of the sacred Mexican mushroom Teonanácatl, crystallizes in the monoclinic space group P21/c with unit-cell dimensions a = 1060(3), b = 853(2), c = 1251(3) pm and β = 91.25(30)°. The structure, solved by direct methods and refined to R = 0.047, shows intermolecular hydrogen bonds between the ethylamino-nitrogen and the indole hydroxy-group. Disorder of the proton in this hydrogen bond indicates the crystal contains a statistical mixture of zwitterions and uncharged species. The molecular conformation of psilocin differs from that found in psilocybin.

Crystal structures of the Teonanácatl hallucinogens. Part I. Psilocybin C12H17N2O4P

Journal of the Chemical Society Perkin Transactions 2 January 1, 1974 Hans Peter Weber, Trevor J. Petcher 20 citations

The hallucinogenic compound psilocybin, found in the sacred Mexican mushroom Teonanácatl, forms crystals that include methanol molecules. The crystal structure shows two psilocybin molecules per asymmetric unit, both existing as zwitterions with different shapes, and a complex network of hydrogen bonds, including very short phosphate-to-phosphate bonds and connections to methanol. The substituents on the indole ring are notably bent out of the plane. Bond lengths were measured with high precision.