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ÈܼÁÑ¡ÏDMSO Æ¥ÅäÈݲ1 (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º70%(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½19¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (+)-pinoresinol di-O-¦Â-D-glucopyranoside C32H42O16 ÏàËÆ¶È:100% Chemical & Pharmaceutical Bulletin 1983 31 2993-2997 The Constituents of Eucommia ulmoides OLIV. I. Isolation of (+)-Medioresinol Di-O-¦Â-D-glucopyranoside TAKESHI DEYAMA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (+)pinoresinol 4,4'-O-bis-D-glucopyranoside ÏàËÆ¶È:100% Chinese Journal of Natural Medicines 2003 1 199-203 Studies on Lignan Constituents of Clematis armandii Franch HUANG Wen-Wu; KONG De-Yun; YANG Pei-Ming Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (+)-pinoresinol-O-¦Â-D-diglucopyranoside ÏàËÆ¶È:100% Chinese Journal of Natural Medicines 2010 8 429-432 Chemical Constituents from the Flower of Datura metel YANG Bing-You; XIA Yong-Gang; CHEN Dong; KUANG Hai-Xue Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (+)-pinores-inol4,4'-O-bis-¦Â-D-glucopyranoside ÏàËÆ¶È:93.7% China Journal of Chinese Materia Medica 2009 34 2761-2764 Chemical constituents of Galium verum ZHAO Chunchao, SHAO Jianhua, CAO Dandan, ZHANG Yuwei LIXian Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (+)-pinoresinol 4,4'-O-bis-¦Â-D-glucopyranoside C32H42O16 ÏàËÆ¶È:93.7% Natural Product Research and Development 2012 24 188-190 WANG Qiong1; LUO Shi-de2; XU Yong-yan1 1 SUN Li-jun; WANG Wei; WANG Yu-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (+)-pinoresinol-¦Â-D-glucoside ÏàËÆ¶È:84.2% Chemical & Pharmaceutical Bulletin 1979 27 2868-2873 Elucidation of the Structure of a New Lignan Glucoside from Olea europaea by Carbon-13 Nuclear Magnetic Resonance Spectroscopy MARIKO CHIBA,KAZUKO OKABE,SUEO HISADA,KATSUHITO SHIMA,TSUNEMATSU TAKEMOTO and SANSEI NISHIBE Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (+)-pinoresinol-¦Â-D-glucoside ÏàËÆ¶È:84.2% Phytochemistry 1980 19 335-336 13CNMR analysis of symplocosin and (+)-epipinoresinol glucoside Mariko Chiba, Sueo Hisada, Sansei Nishibe, H. Thieme Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (+)-pinoresinol-¦Â-D-glucoside C20H22O6 ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 1984 32 4482-4489 Lignans from Bark of Fraxinus mandshurica var. japonica and F. japonica HIROKI TSUKAMOTO,SUEO HISADA and SANSEI NISHIBE Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . scrophenoside C C15H22O8 ÏàËÆ¶È:75% Helvetica Chimica Acta 2004 Vol. 87 598 Phenyl and Phenylethyl Glycosides from Picrorhiza scrophulariiflora Sheng-Xiong Huang, Xun Liao, Quan-Jiang Nie, Li-Sheng Ding, and Shu-Lin Peng Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . scrophenoside C C15H22O8 ÏàËÆ¶È:75% Helvetica Chimica Acta 2004 Vol. 87 598 Phenyl and Phenylethyl Glycosides from Picrorhiza scrophulariiflora Sheng-Xiong Huang, Xun Liao, Quan-Jiang Nie, Li-Sheng Ding, and Shu-Lin Peng Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . coniferin C16H22O8 ÏàËÆ¶È:75% Chemical & Pharmaceutical Bulletin 1991 39 865-870 Studies on the Constituents of the Bark of Kalopanax pictus NAKAI Kazuko SANO,Shuichi SANADA,Yoshiteru IDA and Junzo SHOJI Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (2R)-5,7-dimethoxyflavanone-4'-O-glucoside ÏàËÆ¶È:75% Chemical & Pharmaceutical Bulletin 1988 36 1185-1189 Studies on the Constituents of the European Mistletoe, Viscum album L. II TAKEHIKO FUKUNAGA,IKUKO KAJIKAWA,KOICHI NISHIYA,YOSHIKUNI WATANABE,NOBUO SUZUKI,KOICHI TAKEYA and HIDEJI ITOKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . isoeugenol ¦Â-D-glucopyranoside ÏàËÆ¶È:75% Phytochemistry 1989 28 301-303 Flavonol and phenylpropanoid glycosides from Lilium cordatum Kimiko Nakano,Koji Nishizawa,Ikumi Takemoto,Kotaro Murakami,Yoshihisa Takaishi,Toshiaki Tomimatsu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ËɰØÜÕ ÏàËÆ¶È:75% Chinese Traditional and Herbal Drugs 2010 41 201-203 °×¸½×ӵĻ¯Ñ§³É·ÖÑо¿ °¬·ïΰ; ÕÅáÔ; ÀîÑÞ·ï; ÂíÓ¢Àö Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . coniferin C16H22O8 ÏàËÆ¶È:75% Chinese Traditional and Herbal Drugs 1996 27 259-260 Studies on the Chemical Constituents of Involucrate Balanophora (Balanophora involucrata)(¢ñ) Shen Xiaoling; Shen Yuemao; et al (Department of Phytochemistry; Southwest College of Forestry; Kunming); Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . coniferin ÏàËÆ¶È:75% Archives of Pharmacal Research 1996 19 231-234 Phenolic constituents from the aerial parts of Artemisia stolonifera Kang Ro Lee, Seung Woo Hong, Jong Hwan Kwak, Suhkneung Pyo and Ok Pyo Jee Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (+)-pinoresinol monomethyl ether-¦Â-D-glucoside ÏàËÆ¶È:71.4% Chemical & Pharmaceutical Bulletin 1979 27 2868-2873 Elucidation of the Structure of a New Lignan Glucoside from Olea europaea by Carbon-13 Nuclear Magnetic Resonance Spectroscopy MARIKO CHIBA,KAZUKO OKABE,SUEO HISADA,KATSUHITO SHIMA,TSUNEMATSU TAKEMOTO and SANSEI NISHIBE Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (+)-Medioresinol 4-O-¦Â-D-glucopyranoside ÏàËÆ¶È:71.4% Phytochemistry 1994 35 479-483 Lignans and a stilbene from Festuca argentina Adriana C. Casabuono, Alicia B. Pomillo Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (+)-pinoresinol mono-Me ether-¦Â-D-glucoside ÏàËÆ¶È:71.4% Phytochemistry 1980 19 335-336 13CNMR analysis of symplocosin and (+)-epipinoresinol glucoside Mariko Chiba, Sueo Hisada, Sansei Nishibe, H. Thieme Structure 13C NMR ̼Æ×Ä£Äâͼ |
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