Výsledky vyhledávání - "CHOSAKU YOSHIDA"

Evaluation of Lavender Varietal Characteristics Using Three Content Ratios between Alcohol-based Fragrance Ingredients and Their Derivatives

Autor: Akemitsu Nakatani, Yoshito Seino, Tsuneo Nishikawa, Kazuto Higashimura, Chosaku Yoshida, Akio Suematsu, Yoshiyuki Ban

Publikováno v: Journal of the Japanese Society for Horticultural Science. 77:304-311

We tried to establish an evaluation technique for the varietal characteristics of lavender oil to compare their fragrance components. Nine cultivars of Lavandula angustifolia and 6 cultivars of lavandin (L. angustifolia × L. latifolia) plants were c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::78e76570c050c4e66c59aed58df0a373
https://doi.org/10.2503/jjshs1.77.304

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Synthesis and Antiinflammatory Activity of 7-Methanesulfonylamino-6-phenoxychromones. Antiarthritic Effect of the 3-Formylamino Compound (T-614) in Chronic Inflammatory Disease Models

Autor: T. Inaba, Shuntaro Takano, H. Nagaki, Ryuko Takeno, Keiichi Tanaka, Chosaku Yoshida

Publikováno v: Chemical and Pharmaceutical Bulletin. 48:131-139

A group of derivatives of 7-methanesulfonylamino-6-phenoxychromone (1) at the pyrone and phenoxy rings was synthesized starting with 4-chloro-3-nitroanisole and evaluated against acute and chronic inflammations in oral administration in animals. Sign

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75145a79468c110d586b045b6cfbf876
https://doi.org/10.1248/cpb.48.131

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Pharmacological Studies on 3-Formylamino-7-methylsulfonylamino-6-phenoxy-4H-1-benzopyran-4-one (T-614), a Novel Antiinflammatory Agent. 3rd Communication: The Involvement of Bradykinin in Its Analgesic Actions

Autor: Tomoya Shimotori, Chosaku Yoshida, Keiko Asaoka, Shinji Makino, Ryoko Kitamura, Mariko Eguchi, Keiichi Tanaka

Publikováno v: Journal of Pharmacobio-Dynamics. 15:641-647

In order to elucidate the analgesic mechanism of 3-formylamino-7-methylsulfonylamino-6-phenoxy-4H-1-benzopyran-4-on e (T-614), its effects on the kinin-forming system were examined both in vivo and in vitro. T-614, at doses more than 10 mg/kg p.o., e

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afe333dfde187b26e102bb15b325eea8
https://doi.org/10.1248/bpb1978.15.641

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Pharmacological Studies on 3-Formylamino-7-methylsulfonylamino-6-phenoxy-4H-1-benzopyran-4-one (T-614), a Novel Antiinflammatory Agent. 4th Communication: Inhibitory Effect on the Production of Interleukin-1 and Interleukin-6

Autor: Takihiro Inaba, Yukihiko Aikawa, Keiichi Tanaka, Keiko Asaoka, Chosaku Yoshida, Hiroki Kawasaki

Publikováno v: Journal of Pharmacobio-Dynamics. 15:649-655

In vitro effects of 3-formylamino-7-methylsulfonylamino-6-phenoxy-4H-1-benzopyran-4-on e (T-614), a novel antiinflammatory compound, on the production of interleukin-1 (IL-1) and/or interleukin-6 (IL-6) by human monocytes and the THP-1 cells of a hum

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c04bcceca06d9c7e0d30c564d2082bd0
https://doi.org/10.1248/bpb1978.15.649

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Studies on monocyclic .BETA.-lactam antibiotics. Part I. Synthesis of 4-substituted monocyclic .BETA.-lactams by a lewis acid-mediated reaction

Autor: Kaishu Momonoi, Takako Hori, Kiyoshi Tanaka, Saikawa Isamu, Chosaku Yoshida, Sumiko Kishimoto

Publikováno v: Agricultural and Biological Chemistry. 50:839-846

The synthesis of 4-substituted monocyclic α-lactam is described. The key step in this method was accomplished by nucleophilic replacement in the presence of Lewis acid, that is, (3S,4S)-4-acetoxy-3-phenylacetamido-2-azetidinone derivatives or oxazol

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7c0cabb7e8536bc6973d9f2d89e27224
https://doi.org/10.1271/bbb1961.50.839

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STUDIES ON MONOCYCLIC β-LACTAM ANTIBIOTICS

Autor: Rikizo Hattori, Chosaku Yoshida, Saikawa Isamu, Sumiko Kishimoto, Yoshikazu Fukuoka, Kiyoshi Tanaka, Komatsu Miwako

Publikováno v: The Journal of Antibiotics. 39:215-229

The synthesis and antibacterial activity of the 3-[2-(2-aminothiazol-4-yl)-( Z)-2-(O-substituted oxyimino)acetamido]-1-(1H-tetrazol-5-yl)-2-azetidinones having various functional groups at C-4 position of β-lactam are described. These compounds exhi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1c065a0ab907f656f1764a9e1b1db7b1
https://doi.org/10.7164/antibiotics.39.215

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