Masao Yoshizaki
University of Toyama
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Featured researches published by Masao Yoshizaki.
Phytochemistry | 1992
Takuo Okuda; Takashi Yoshida; Tsutomu Hatano; Mayumi Iwasaki; Makiko Kubo; Teruyo Orime; Masao Yoshizaki; Naohiro Naruhashi
Abstract A HPLC survey of leaves of 80 plants (62 species, 15 hybrids, one variety and two cytotypes) from 18 genera of four subfamilies of Rosaceae, using five oligomeric hydrolysable tannins, five monomeric hydrolysable tannins, and chlorogenic acid as reference compounds, showed that the oligomers can be used as chemotaxonomic markers for the family, viz., sanguiin H-6 and H-11 in the genera Sanguisorba and Rubus , gemin A in Geum , agrimoniin in Agrimonia , Fragaria and Potentilla , and rugosin D in Filipendula . The hydrolysable tannin monomers were widely distributed in the herbaceous and frutescent Rosoideae species, but not in the arborous species of the other subfamilies. Chlorogenic acid was found in almost all of the plants examined.
Tetrahedron Letters | 1987
Toshimitsu Hayashi; Mieko Kishi; Masaru Kawasaki; Munehisa Arisawa; Mineo Shimizu; Shoichi Suzuki; Masao Yoshizaki; Naokata Morita; Yasuhiro Tezuka; Tohru Kikuchi; Luis H. Berganza; Esteban Ferro; Isabel Basualdo
Abstract Scopadulcic acid-A and -B, diterpenoids with a novel skeleton, have been isolated from the whole plants of Scopari dulcis L., and their structures, including the absolute configuration, were determined based on the 2-D NMR and CD spectral data.
Phytochemistry | 1987
Masao Yoshizaki; Tetsuro Shingu; Takuo Okuda; Tsutomu Hatano; Tamami Kaneda
Abstract A new ellagitannin, named liquidambin, which could be biogenetically closely correlated with casuarinin and pedunculagin, has been isolated from the leaves of Liquidambar formosana . Its structure was determined as 5- O -galloyl-2,3,4,6-di- O -(S)-hexahydroxydiphenoyl- d -glucose. The structural equilibration due to hydration of the aldehyde group of the glucose core in this tannin was shown from its 1 H and 13 C NMR spectra.
Phytochemistry | 1987
Masao Yoshizaki; Hiroharu Fujino; Mihoko Masuyama; Munehisa Arisawa; Naokata Morita
Abstract The 7-, 3′- and 4′-glucosides of luteolin, the 7-glucoside and 6,8-di- C -glucoside of apigenin were isolated from Trichosanthes kirilowii var. japonica . Kaempferol 3,7-di-rhamnoside and 3-glucoside-7-rhamnoside were identified from T. cucumeroides , kaempferol 3-galactoside and 3-sophoroside were also identified from T. anguina . Quercetin-3-rutinoside was detected from T. multiloba and T. rostrata. T. bracteata afforded luteolin 3′-glucoside and kaempferol 3-rutinoside, and T. kirilowii afforded luteolin 7-, 3′- and 4′-glucosides and apigenin 7-glucoside.
Journal of Natural Products | 1988
Hajime Ueno; Syunji Horie; Yumiko Nishi; Hisashi Shogawa; Masaru Kawasaki; Shoichi Suzuki; Toshimitsu Hayashi; Munehisa Arisawa; Mineo Shimizu; Masao Yoshizaki; Naokata Morita; Luis H. Berganza; Esteban Ferro; Isabel Basualdo
Japanese Journal of Pharmacology | 1984
Masayasu Kimura; Ikuko Kimura; Kazuyoshi Takahashi; Masashi Muroi; Masao Yoshizaki; Matao Kanaoka; Isao Kitagawa
Chemical & Pharmaceutical Bulletin | 1989
Mineo Shimizu; Syunji Horie; Satoshi Terashima; Hajime Ueno; Toshimitsu Hayashi; Munehisa Arisawa; Shoichi Suzuki; Masao Yoshizaki; Naokata Morita
Chemical & Pharmaceutical Bulletin | 1990
Mineo Shimizu; Hisashi Shogawa; Takayasu Matsuzawa; Sakiko Yonezawa; Toshimitsu Hayashi; Munehisa Arisawa; Shoichi Suzuki; Masao Yoshizaki; Naokata Morita; Esteban Ferro; Isabel Basualdo; Luis H. Berganza
Planta Medica | 1974
Tsuneo Namba; Masao Yoshizaki; Tsuyoshi Tomimori; Kyoichi Kobashi; K. Mitsui; J. Hase
Chemical & Pharmaceutical Bulletin | 1991
Mineo Shimizu; Takayasu Matsuzawa; Syoichi Suzuki; Masao Yoshizaki; Naokata Morita