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²éѯ½á¹û£º¹²²éµ½17¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 6'-[(E)-2''-hydroxymethyl, 2''-butenoyl] arbutin C17H22O9 ÏàËÆ¶È:100% Journal of Asian Natural Products Research 2006 8 373-377 Phenolic glycosides from leaves of Hopiciopsis lobata Q.-Q. HE, M.-S. LIU, D.-J. JIN and L.-Y. KONG Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . eximine ÏàËÆ¶È:80% Journal of Natural Products 1999 62 1526-1531 Polyphenolic Glycosides from African Proteaceae L. Verotta, F. Orsini, F. Pelizzoni, G. Torri, and C. B. Rogers Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 4-hydroxyphenyl-(6'-O-benzoyl)-O-¦Â-D-glucopyranoside ÏàËÆ¶È:80% Phytochemical Analysis 2002 13 283-292 Biflavonoids and a glucopyranoside derivative from Ouratea semiserrata Javier Rincon Velandia, M¨¢rio Geraldo de Carvalho, Raimundo Braz-Filho and Alceni A. Werle Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Hydroquinone O-[6-(3-hydroxyisobutanoyl)]-¦Â-galactopyranoside C16H22O9 ÏàËÆ¶È:73.3% Phytochemistry 2010 71 325-331 Glycosides from Breynia fruticosa and Breynia rostrata Dahai Meng, Jian Wu, Weimin Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 8 C19H20O9 ÏàËÆ¶È:73.3% Pharmazie 1998 53 280-281 Flavan-di-O-gallates and further polyphenols from Sedum stoloniferum F.PETEREIT,M.K.SAKAR and A.NAHRSTEDT Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 6-O-galloylarbutin ÏàËÆ¶È:73.3% Chinese Traditional and Herbal Drugs 2012 43 1704-1707 Chemical constituents from rhizomes of Bergenia scopulosa (¢ò) CUI Ying Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 6'-O-galloylarbutin C19H20O11 ÏàËÆ¶È:73.3% Journal of Chinese Medicinal Materials 2005 28 23-24 ÇØÁëÑҰײ˻¯Ñ§³É·ÖÑо¿(¢ò) Íõ¾üÏÜ, ÂÀÐÞ÷ Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 6-O-galloylarbutin C19H20O11 ÏàËÆ¶È:66.6% Natural Product Research and Development 2005 17 177-178 Studies on the Chemical Constituents from Herba Polygonum viviparum L. ZHANG Cai-xia; LI Yu-lin; HU Feng-zu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . arbutin,1-acetate ÏàËÆ¶È:66.6% Journal of Chinese Medicinal Materials 2012 35 1080-1082 Study on the Chemical Constituents of Herpetospermum caudigerum XU Bing, YANG Pan-pan, WANG Pei-long, LING Hu-lang, CHEN Min Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3,4-dihydroxyphenyl-(6'-O-benzoyl)-O-¦Â-D-glucopyranoside C19H20O9 ÏàËÆ¶È:64.7% Journal of Natural Products 1999 62 1526-1531 Polyphenolic Glycosides from African Proteaceae L. Verotta, F. Orsini, F. Pelizzoni, G. Torri, and C. B. Rogers Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 6'-O-p-hydroxybenzoylarbutin ÏàËÆ¶È:64.7% Natural Medicines 1996 50 404-407 Studies on Nepalese Crude Drugs. XXII : On the Phenolic Constituents of the Rhizome of Bergenia ciliata (HAW.) STERNB. FUJII MASAYUKI,MIYAICHI YUKINORI,TOMIMORI TSUYOSHI Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 6'-O-protocatechuoylarbutin C19H20O10 ÏàËÆ¶È:64.7% Natural Medicines 1996 50 404-407 Studies on Nepalese Crude Drugs. XXII : On the Phenolic Constituents of the Rhizome of Bergenia ciliata (HAW.) STERNB. FUJII MASAYUKI,MIYAICHI YUKINORI,TOMIMORI TSUYOSHI Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . p-hydroxybenzoylarbutin ÏàËÆ¶È:64.7% Journal of Shenyang Pharmaceutical University 2014 31 673-676 Chemical constituents from the stems and leaves of Sedum aizoon L. (¢ò) JIA Ling-yun, XU Tan-ye, WANG Jing, L¨¹¦a Chong-ning, LU Jin-cai Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 6'-(2,5-Dihydroxycinnamoyl) arbutin C21H22O10 ÏàËÆ¶È:63.1% Natural Product Research 2010 24 1861-1864 Cytotoxic clerodane diterpenoids from the leaves of Polyalthia longifolia Koneni V. Sashidhara; Suriya P. Singh; Jayanta Sarkar; Sudhir Sinha Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . pseudolaroside B C14H18O9 ÏàËÆ¶È:60% Phytochemistry 2006 67 1395-1398 Benzoic acid allopyranosides from the bark of Pseudolarix kaempferi Peng Liu, Hongzhu Guo , Yin Tian, Qiao Wang, Dean Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . p-hydroxyphenyl-O-¦Â-D-primeveroside ÏàËÆ¶È:60% Journal of Natural Products 1993 Vol 56 1421 p-Hydroxyphenyl-O-¦Â-D-primeveroside, a Novel Glycoside Formed from Hydroquinone by Cell Suspension Cultures of Rauwolfia serpentina Ralf Lutterbach, Joachim Stöckigt, Heinz Kolshorn Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . pyroside ÏàËÆ¶È:60% Journal of Shenyang Pharmaceutical University 2014 31 673-676 Chemical constituents from the stems and leaves of Sedum aizoon L. (¢ò) JIA Ling-yun, XU Tan-ye, WANG Jing, L¨¹¦a Chong-ning, LU Jin-cai Structure 13C NMR ̼Æ×Ä£Äâͼ |

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