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NTIS 바로가기Chemical & pharmaceutical bulletin, v.49 no.1, 2001년, pp.69 - 72
MATSUDA, Hisashi (Kyoto Pharmaceutical University) , OHTA, Toshio (Kyoto Pharmaceutical University) , KAWAGUCHI, Atsuhiro (Kyoto Pharmaceutical University) , YOSHIKAWA, Masayuki (Kyoto Pharmaceutical University)
Five paeonol glycosides, suffruticosides A, B, C, D, and E, and a monoterpene glucoside, galloyl-oxypaeoniflorin, were isolated from the glycosidic fraction of Chinese Moutan Cortex, the root cortex of Paeonia suffruticosa Andrews, together with paeonolide, apiopaeonoside, galloyl-paeoniflorin, oxyp...
10.1248/cpb.48.1327 1) Part V: Yoshikawa M., Ohta T., Kawaguchi A., Matsuda H., Chem. Pharm. Bull., 48, 1327-1331 (2000).
10.1016/S0960-894X(99)00536-3 2) a) Matsuda H., Kageura T., Toguchida I., Murakami T., Kishi A., Yoshikawa M., Bioorg. Med. Chem. Lett., 9, 3081-3086 (1999)
10.1248/cpb.47.340 b) Yoshikawa M., Morikawa T., Murakami T., Toguchida I., Harima S., Matsuda H., Chem. Pharm. Bull., 47, 340-345 (1999)
c) Murakami T., Matsuda H., Inadzuki M., Hirano K., Yoshikawa M., ibid., 47, 1717-1724 (1999)
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4) a) This work was reported in our preliminary communication<SUP>4b)</SUP>
10.1248/cpb.40.2248 b) Yoshikawa M., Uchida E., Kawaguchi A., Kitagawa I., Yamahara J., Chem. Pharm. Bull., 40, 2248-2250 (1992).
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b) Kariyone T., Takahashi M., Takaishi K., ibid., 76, 917-919 (1956).
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10.1016/S0040-4020(01)88953-5 b) Kaneda M., Iitaka Y., Shibata S., Tetrahedron, 28, 4309-4317 (1972).
10) The <SUP>1</SUP>H- and <SUP>13</SUP>C-NMR spectra of suffruticosides (1,2,4,5,7) and galloyl-oxypaeoniflorin (8) were assigned with the aid of distortionless enhancement by polarization transfer (DEPT), homo correlation spectroscopy (<SUP>1</SUP>H-<SUP>1</SUP>H COSY), and homonuclear Hartman-Hahn spectroscopy (<SUP>1</SUP>H-<SUP>1</SUP>H HOHAHA).
12) Uchiyama M., Suzuki Y., Fukuzawa K., Yakugaku Zasshi, 88, 678-683 (1968).
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