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Psilocybin: all studies

Page 184 of 441: studies 1,831 to 1,840 of 4,401, newest first. Back to the psilocybin overview

Research

Discrimination of Psychoactive Fungi (Commonly Called "Magic Mushrooms") Based on the DNA Sequence of the Internal Transcribed Spacer Region.

Food Hygiene and Safety Science (Shokuhin Eiseigaku Zasshi) 2003 Takuro Maruyama, Osamu Shirota, Nobuo Kawahara et al. 14 citations

'Magic mushrooms' (MMs) are psychoactive fungi containing the hallucinogenic compounds, psilocin (1) and psilocybin (2). Since June 6, 2002, these fungi have been regulated by the Narcotics and Psychotropics Control Law in Japan. Because there are many kinds of MMs and they are sold even as dry powders in local markets, it is very difficult to identify the original species of the MMs by...

DOI: 10.3358/shokueishi.44.44 (opens in new tab) Internal transcribed spacer Sequence biology Genetics

The pharmacology of psilocybin

Addiction Biology October 1, 2002 Torsten Passie, Juergen Seifert, Udo Schneider et al. 465 citations

Abstract Psilocybin (4‐phosphoryloxy‐N,N‐dimethyltryptamine) is the major psychoactive alkaloid of some species of mushrooms distributed worldwide.These mushrooms represent a growing problem regarding hallucinogenic drug abuse. Despite its experimental medical use in the 1960s, only very few pharmacological data about psilocybin were known until recently. Because of its still growing capacity...

Synthesis of a psilocin hapten and a protein-hapten conjugate

Journal of Pharmacy and Pharmacology September 1, 2002 Christian Albers, Matthias Lehr, Justus Beike et al. 7 citations

Abstract Derivatives of psilocin with ω-functionalized alkyl spacers in position 1 of the indole ring were synthesized as haptens for use in a radioimmunoassay. Whereas the psilocin analogues with a 3-aminopropyl and a 4-aminobutyl moiety at the indole nitrogen decomposed during synthesis, the analogous 3-carboxypropyl psilocin derivative proved to be stable. This compound was coupled to bovine...

Renal excretion profiles of psilocin following oral administration of psilocybin: a controlled study in man

Journal of Pharmaceutical and Biomedical Analysis August 26, 2002 Felix Hasler, Daniel Bourquin, Rudolf Brenneisen et al. 100 citations

In a clinical study eight volunteers received psilocybin (PY) in psychoactive oral doses of 212+/-25 microg/kg body weight. To investigate the elimination kinetics of psilocin (PI), the first metabolite of PY, urine was collected for 24 h and PI concentrations were determined by high-performance liquid chromatography with column switching and electrochemical detection (HPLC-ECD). Sample workup...

Synthetic studies of psilocin analogs having either a formyl group or bromine atom at the 5- or 7-position.

Chemical and Pharmaceutical Bulletin January 2002 Fumio Yamada, Mayumi Tamura, Atsuko Hasegawa et al.

Psilocin analogs having either a formyl group (9-12) or a bromine atom (13-18) at the 5- or 7-position have been prepared for the first time. Syntheses of 5- and 7-bromo derivatives of 4-hydroxy- (23, 24, 28) and 4-benzyloxyindole-3-carbaldehyde (19, 25, 29, 30), 4-benzyloxyindole-3-acetonitriles (20, 31), and 4-benzyloxy-N,N-dimethyltryptamine (32, 34, 35) have also been established.

Effects of the Hallucinogen Psilocybin on Covert Orienting of Visual Attention in Humans

Neuropsychobiology 2002 Euphrosyne Gouzoulis‐mayfrank, B. Thelen, Stefanie Maier et al. 69 citations

Hallucinogenic drug-induced states are considered as models for acute schizophrenic disorders (experimental psychoses). In a double-blind study with healthy volunteers we investigated the influence of the serotonergic hallucinogen psilocybin, the ecstasy-like drug 3,4-methylenedioxyethylamphetamine (MDE), the stimulant d- methamphetamine and placebo on covert orienting of spatial attention (n =...

Towards a molecular approach for the identification of fungal taxa that contain psilocybin

OpenGrey 2001 Lee Jc 2 citations

The classical taxonomic methodologies for determining taxa of mushrooms are based primarily on morphological traits. If the mushroom specimens are dried or pulverized, the morphological characteristics are frequently disguised or no longer apparent. Included among these fungi are known to produce psilocybin, which are hard to identify by their macroscopic features. Molecular techniques could...

DOI: 10.48730/zty1-g223 (opens in new tab) Psilocybin Identification biology Taxon Evolutionary biology +3

What the clinician needs to know about magic mushrooms

Advances in Psychiatric Treatment September 1, 2000 Nicholas Seivewright, Olawale Lagundoye 3 citations

This term refers to mushrooms that grow naturally and have hallucinogenic (sometimes called psychedelic) properties. Consumption of different species has occurred in various cultures over the centuries, with use in ritual ceremonies in Mexico being particularly well known. In the UK at present the species most commonly used is Psilocybe semilanceata , also known as the ‘liberty cap’ mushroom....

DOI: 10.1192/apt.6.5.344 (opens in new tab) Full text (opens in new tab) Magic telescope Mushroom Traditional medicine Botany

Psilocybin and Psilocin

March 9, 2000 John C.m. Brust

Abstract Psilocybin and psilocin are indolealkylamines present in Central American Psilocybe species of mushrooms and in Panaeolus mushroom species of the United States (3,4). For thousands of years, Mexican Native Americans have eaten Psilocybe mushrooms ritualistically for their hallucinatory and psychedelic (“mind-revealing”) properties. In the United States during the 1980s, recreational...

ChemInform Abstract: Improvements to the Synthesis of Psilocybin and a Facile Method for Preparing the O‐Acetyl Prodrug of Psilocin.

ChemInform August 17, 1999 David E. Nichols, Steward Frescas 2 citations

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

DOI: 10.1002/chin.199933137 (opens in new tab) Psilocybin Combinatorial chemistry Prodrug Nanotechnology +1