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Osamu Shirota

5 papers in the library · 284 citations · publishing 2003-2009

Papers

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Effects ofPsilocybe argentipeson Marble-Burying Behavior in Mice

Bioscience Biotechnology and Biochemistry August 23, 2009 Yoshihiro Matsushima, Osamu Shirota, Ruri Kikura-Hanajiri et al. 77 citations

Psilocybe argentipes is a hallucinogenic mushroom. The present study examined the effects of P. argentipes on marble-burying behavior, which is considered an animal model of obsessive-compulsive disorder. P. argentipes significantly inhibited marble-burying behavior without affecting locomotor activity as compared with the same dose of authentic psilocybin. These findings suggest that P....

DOI: 10.1271/bbb.90095 (opens in new tab) Full text (opens in new tab) Psilocybin Obsessive compulsive Animal model Hallucinogen +1

Neo-clerodane diterpenes from the hallucinogenic sage Salvia divinorum.

Journal of Natural Products December 1, 2006 Osamu Shirota, Kumi Nagamatsu, Setsuko Sekita 68 citations

Seven new neo-clerodane diterpenes, salvidivins A (2), B, (3), C (4), and D (5), salvinorins H (6) and I (7), and divinatorin [corrected] F (8), along with eight known neo-clerodane diterpenes, salvinorins A (1)-F, divinatorins A and B, and seven other constituents, were isolated from the hallucinogenic sage Salvia divinorum. The structures of 1-7 were elucidated on the basis of 2D NMR...

DOI: 10.1021/np060456f (opens in new tab) Full text (opens in new tab) Salvia divinorum chemistry Salvia divinorum compounds Salvia divinorum phytochemistry Salvia divinorum constituents +10

Determination of psilocybin in hallucinogenic mushrooms by reversed-phase liquid chromatography with fluorescence detection

Talanta January 7, 2005 Kimie Saito, Toshimasa Toyo’oka, Masaru Kato et al. 35 citations

The determination of psilocybin was carried out by reversed-phase liquid chromatography (HPLC) with fluorescence (FL) detection. Psilocybin was labeled with 5-dimethylaminonaphthalene-1-[N-(2-aminoethyl)]sulfonamide (DNS-ED) at 60 degrees C for 4h in the presence of 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) as the activation reagent. The resulting derivative was separated on a...

DOI: 10.1016/j.talanta.2004.11.031 (opens in new tab) Psilocybin Hallucinogen Reversed-phase chromatography Fluorescence spectroscopy +1

Concise Large-Scale Synthesis of Psilocin and Psilocybin, Principal Hallucinogenic Constituents of “Magic Mushroom”

Journal of Natural Products May 30, 2003 Osamu Shirota, Wataru Hakamata, Yukihiro Goda 90 citations

The concise large-scale syntheses of psilocin (1) and psilocybin (2), the principal hallucinogenic constituents of "magic mushroom", were achieved without chromatographic purification. The key step in the synthesis of 2 was the isolation of the dibenzyl-protected intermediate (7) as a zwitterionic derivative (8), which was completely identified by means of 2D NMR analyses.

DOI: 10.1021/np030059u (opens in new tab) Psilocybin Hallucinogen Mushroom Stereochemistry

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