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1 .     saposide A
C32H44O16     ÏàËÆ¶È:67.6%
Molecules          2013          18          9641-9649
Phenylpropanoid, Sapnol A, Lignan and Neolignan Sophorosides, Saposides A and B, Isolated from Canadian Sugar Maple Sap
Kazuko Yoshikawa, Sakiko Tani, Chihiro Baba and Toshihiro Hashimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     flacoside B
C32H44O15     ÏàËÆ¶È:61.7%
Planta Medica          2009          75          1246-1252
Investigation of Two Flacourtiaceae Plants: Bennettiodendron leprosipes and Flacourtia ramontchi
Xing-Yun Chai, Hong-Yan Ren, Zheng-Ren Xu, Chang-Cai Bai, Fei-Ran Zhou, Si-Kai Ling, Xiao-Ping Pu, Fei-Fei Li,Peng-Fei Tu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     Repenins A
C29H24O10     ÏàËÆ¶È:61.7%
Bioorganic & Medicinal Chemistry Letters          2009          19          3521-3524
Repenins A¨CD, four new antioxidative coumarinolignoids from Duranta repens Linn.
Nisar Ahmad, Fozia Zeb, Ijaz Ahmad, Fanghai Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     chionoside A
C35H46O20     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2010          58          703-711
Phenylethanoid and Iridoid Glycosides in the New Zealand Snow Hebes (Veronica, Plantaginaceae)
Rilka M. Taskova, Tetsuo Kokubun, Ken G. Ryan, Phil John Garnock-Jones and Soren Rosendal Jensen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     (-)-(7'S,8'S)-threo-carolignan X
C39H40O12     ÏàËÆ¶È:58.9%
Journal of Natural Products          2010          73          1649-1654
Lignans and Triterpenes from the Bark of Durio carinatus and Durio oxleyanus
Rudiyansyah, Lynette K. Lambert, and Mary J. Garson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     scroside E
C30H38O16     ÏàËÆ¶È:58.8%
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   Ì¼Æ×Ä£Äâͼ

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7 .     kaempferol-3-O-(2-O-trans-p-methoxycoumaroyl-6-O-trans-p-coumaroyl)-¦Â-D-glucopyranoside
C40H34O15     ÏàËÆ¶È:58.8%
Phytochemistry          2008          69          2070-2080
Phenolic compounds and rare polyhydroxylated triterpenoid saponins from Eryngium yuccifolium
Zhizhen Zhang, Shiyou Li,Stacy Ownby, Ping Wang, Wei Yuan, Wanli Zhang, R. Scott Beasley
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     litseaefoloside C
C30H30O14     ÏàËÆ¶È:58.8%
Journal of Natural Products          2005          68          1531-1535
Phenolic and Triterpene Glycosides from the Stems of Ilex litseaefolia
Ai-Lian Zhang, Qi Ye, Bo-Gang Li, Hua-Yi Qi, and Guo-Lin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     (+)-isolariciresinol-9'-(2-p-coumaric)-O-¦Â-D-xylopyranoside
C34H38O12     ÏàËÆ¶È:58.8%
Acta Botanica Yunnanica          2006          28(4)          433-437
Lignans and Triterpenoids from Cissus repens ( Vitaceae)
WANG Yue-Hu,, ZHANG Zhong-Kai,HE Hong-Ping, GAO Suo, KONGNing-Chuan, DINGMing, HAO Xiao-Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     kaempferol-3-O-[2-O-(6-O-E-feruloyl)-¦Â-D-glucopyranosyl]-¦Â-galactopyranoside
     ÏàËÆ¶È:58.8%
China Journal of Chinese Materia Medica          2007          32          590-593
Studies on constituents of Oldenlandia diffusa
ZHOU Yingjun, WU Kongsong, ZENG Guangyao, TAN Jianbing, XU Kangping, LI Fushuang, TAN Guishan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     quercetin 3-(6''-caffeoylgalactoside)
     ÏàËÆ¶È:58.8%
Phytochemistry          1982          21          2156-2158
Quercetin 3-(6''-caffeoylgalactoside) from Hydrocotyle sibthorpioides
Nobuharu Shigematsu, Isao Kouno, Nobusuke Kawano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     helichrysoside
     ÏàËÆ¶È:58.8%
Chinese Traditional and Herbal Drugs          2009          40          704-708
ÕäÖé²Ë»¯Ñ§³É·ÖµÄÑо¿
×Þº£ÑÞ;ÍÀÅô·É
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     compound 12
C32H32O13     ÏàËÆ¶È:58.8%
Tetrahedron          1991          47          6717-6724
Research on African medicinal plants. XXVII. Interjectin a derivative of nyasicoside from Hypoxis interjecta and Hypoxis multiceps
Giovanni B. Marini-Bettolo, Corrado Galeffi, Giuseppina Multari, Giovanna Palazzino, Irene Messana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     quercetin-7-O-¦Â-D-[6''-O-(trans-feruloyl)]-glucopyranoside
C31H28O15     ÏàËÆ¶È:58.8%
Journal of Integrative Plant Biology          2006          48          359-363
A Novel Flavonoid Glucoside from Anoectochilus roxburghii (Wall.) Lindl.
Chun-Nian He, Chun-Lan Wang, Shun-Xing Guo*, Jun-Shan Yang and Pei-Gen Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     quercetin 4'-O-¦Â-D-(6''-E-caffeoyl)-glucopyranoside
     ÏàËÆ¶È:58.8%
Food Chemistry          2012          130          165-170
Anti-complementary activity of flavonoids from Gnaphalium affine D. Don
Zhongxin Xi, Wansheng Chen, Zhijun Wu, Yan Wang, Peiyuan Zeng, Guijun Zhao, Xia Li, Lianna Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     matairesinol-4'-O-¦Â-gentiobioside
C32H42O16     ÏàËÆ¶È:58.8%
China Journal of Chinese Materia Medica          2012          37          1581-1585
Trace chemical constituents contained in Trachelospermum jasminoides and structure identification
JING Ling; YU Nengjiang; ZHAO Yimin; LI Yushan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     quercetin-3-O-(6''-O-trans-p-coumaroyl)-¦Â-D-glucopyranoside
C30H26O14     ÏàËÆ¶È:58.8%
Journal of Shenyang Pharmaceutical University          2013          30          171-177
Isolation and identification of constituents from whole plant of Leontopodium leontopodioides (Willd.) Beauv. (III)
CHEN Qiu, WANG Tao, WU Chun-hua, Kaunda Joseph Sakah, HAN Li-feng, ZHANG Yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     Matairesinol 4'-O-¦Â-D-cellobioside
C32H42O16     ÏàËÆ¶È:58.8%
Acta Pharmaceutica Sinica B          2013          3          109-112
A new lignan and active compounds inhibiting NF-¦ÊB signaling pathway from Caulis Trachelospermi
Chencheng Zhu, Ling Jing, Nengjiang Yu, Xuedong Yang, Yimin Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-{6-O-[(E)-3-(4-hydroxy-3-methoxyphenyl)pro-2-enoyl]-¦Â-D-glucopyranosyloxy}-4H-1-benzopyran-4-one
     ÏàËÆ¶È:58.8%
Helvetica Chimica Acta          1993          76          2981-2991
Chemo-enzymatic Synthesis of 6¡å-O-(3-Arylprop-2-enoyl) Derivatives of the Flavonol Glucoside Isoquercitrin
Bruno Danieli, Andrea Bertario, Giacomo Carrea, Barbara Redigolo, Francesco Secundo and Sergio Riva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     verpectoside A
C35H46O19     ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          2002          50(5)          665-668
New Phenylethanoid Glycosides from Veronica pectinata var. glandulosa and Their Free Radical Scavenging Activities
Iclal SARACOGLU,Ummuhan Sebnem HARPUT,Makoto INOUE,and Yukio OGIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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