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(1) 56.31,56.54,61.78,69.63,70.28,70.86,70.95,72.61,72.85,79.07,79.12,81.79,81.98,90.23,91.07,103.09,104.13,104.64,109.66,109.74,116.02,121.01,128.61,156.76,156.87,159.60,160.34,161.35,163.76,163.91,164.99,182.00,182.33
(2)
44.80,45.11,45.60,46.56,56.47,56.55,62.90,63.85,65.57,71.50,73.80,74.28,75.55,75.78,79.72,89.49,94.65,109.90,113.29,113.51,115.63,115.83,121.78,122.05,131.89,132.15,146.04,146.21,148.58,148.79,173.29,175.74
(3)
16.25,17.22,17.78,17.97,18.10,22.96,24.38,26.02,31.51,36.79,40.51,40.65,42.01,50.74,52.59,61.92,63.05,71.35,71.85,72.02,75.55,75.65,77.83,78.09,78.37,79.24,80.00,81.09,85.07,98.45,105.72,126.00,132.44
(4)
55.97,56.37,69.57,73.13,76.46,77.26,95.02,99.50,99.98,103.45,104.47,105.35,109.54,110.28,115.78,120.47,121.30,148.07,148.22,150.97,156.93,161.11,162.98,164.17,182.08
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karl2100: ½ð±Ò+1, лл£¡ 2013-03-24 00:49:47
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1 .     swertisin
C22H22O10     ÏàËƶÈ:96.9%
Molecules          2012          17          7914-7926
Variable-Temperature 1H-NMR Studies on Two C-Glycosylflavones
Julia H. Frank, Yomica L. Powder-George, Russel S. Ramsewak and William F. Reynolds
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     apigenin-6-C-¦Â-D-glucoside-7-O-methyl ether
    ÏàËƶÈ:87.8%
Natural Product Communications          2006          1          457-459
Flavonoid C-glycosides from Pterocephalus sanctus Growingin Egypt
Fahem A. Ahmed and Abdelaaty A. Shahat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     luteolin-6-C-¦Â-D-glucoside-7-O-methyl ether
    ÏàËƶÈ:84.8%
Natural Product Communications          2006          1          457-459
Flavonoid C-glycosides from Pterocephalus sanctus Growingin Egypt
Fahem A. Ahmed and Abdelaaty A. Shahat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     4'-O-(E)-sinapoyl-7-methoxyisovitexin-2''-O-¦Â-D-glucopyranoside
    ÏàËƶÈ:67.6%
Phytochemistry          2010          71          581-589
Metabolic responses of Thellungiella halophila/salsuginea to biotic and abiotic stresses: Metabolite profiles and quantitative analyses
M. Soledade C. Pedras, Qing-An Zheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     4'-O-(E)-sinapoyl-7-methoxyisovitexin-2''-O-¦Â-D-glucopyranoside
    ÏàËƶÈ:67.6%
Phytochemistry          2010          71          581-589
Metabolic responses of Thellungiella halophila/salsuginea to biotic and abiotic stresses: Metabolite profiles and quantitative analyses
M. Soledade C. Pedras, Qing-An Zheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     apigenin-7-O-¦Â-apiofuranosyl-6, 8-di-C-¦Â-glucopyranoside
C32H38O19     ÏàËƶÈ:66.6%
Phytochemistry          2003                   449-452
Flavone C-glycosides from Lupinus hartwegii
Mohamed S. Kamel
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     6-C-[¦Á-L-arabinopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl]-7-O-[¦Â-D-glucopyranosyl]-luteolin 3'-methyl ether
C33H40O20     ÏàËƶÈ:66.6%
Natural Product Communications          2011          6          205-208
Secondary Metabolites from the Roots of Paronychia chionaea
Sibel Avunduk, Özgen Alankuş-Çalişkan, Tomofumi Miyamoto, Chiaki Tanaka and Marie-Aleth Lacaille-Dubois
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     apigenin 6-C-neohesperidoside
    ÏàËƶÈ:66.6%
Phytochemistry Letters          2012          5          427-431
Flavonoids from Mimosa xanthocentra (Leguminosae: Mimosoideae) and molecular modeling studies for isovitexin-2¡å-O-¦Á-l-rhamnopyranoside rotamers
Luiza Maria de Magalhães Camargo, Jean-Pierre F¨¦r¨¦zou, Luzineide Wanderley Tinoco, Carlos Roland Kaiser, Sônia Soares Costa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     6'''-feruloylspinosin
C38H40O18     ÏàËƶÈ:63.8%
Tetrahedron          2000          56          8915-8920
Flavonoids from Ziziphus jujuba Mill var. spinosa
Gong Cheng, Yanjing Bai, Yuying Zhao, Jing Tao, Yi Liu, Guangzhong Tu, Libin Ma, Ning Liao, Xiaojie Xu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     6'''-feruloylspinosin
    ÏàËƶÈ:63.8%
Korean Journal of Pharmacognosy          2012          43          127-136
Flavonoids from the Seeds of Zizyphus jujuba var. spinosa
Lee, So-Young; Lee, Joo-Young; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     isovitexin 2''-O-(6'''-(E)-p-coumaroyl)glucoside
C36H36O17     ÏàËƶÈ:63.6%
Phytochemistry          2001          58          167-172
Acylated flavone C-glycosides from Cucumis sativus
Mamdouh M. Abou-Zaid, Domenic A. Lombardo, Geoffrey C. Kite,Ren¨¦e J. Grayerb, Nigel C. Veitch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     embinoidin
    ÏàËƶÈ:63.6%
Phytochemistry Letters          2010          3          88-92
Isolation and structure elucidation of flavonoid glycosides from Solanum verbascifolium
Takashi Ohtsuki, Takashi Miyagawa, Takashi Koyano, Thaworn Kowithayakorn, Masami Ishibashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     swertisin 2''-O-rhamnoside-4''-O-glucoside
C34H42O19     ÏàËƶÈ:63.6%
Phytochemistry          1999          51          1395-1399
Novel pigments and copigmentation in the blue marguerite daisy
Stephen J. Bloor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     vaccarin(Íõ²»ÁôÐлÆͪÜÕ)
C32H38O19     ÏàËƶÈ:63.6%
Chinese Traditional and Herbal Drugs          2011          42(5)          874-876
Isolation and identification of vaccarin from Vaccariae Semen
MENG He, CHEN Yu-ping, QIN Wen-jie, YE Zu-guang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     2"-O-Glucosyl-isovitexin-7-O-galactosid
    ÏàËƶÈ:63.6%
Phytochemistry          1979          18          907-910
Neue flavon-C-O-glykoside aus Melandrium album
Hildebert Wagner, G¨¹nther Obermeier, Otto Seligmann, Vedantha Mohan Chari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     6'''-feruloylspinosin
C38H40O18     ÏàËƶÈ:63.6%
Phytochemistry          1980          19          2791-2793
Acylated flavone-C-glycosides from the seeds of Zizyphus jujuba
Won Sick Woo, Sam Sik Kang, Hildebert Wagner, Otto Seligmann, V.M. Chari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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1 .     6-acetyl-1-[1,3-(4,4'-dihydroxy-3,3'-dimethoxy-¦Â-truxinyl)-¦Â-D-fructofuranosyl]-¦Á-D-glucopyranoside
C34H40O18     ÏàËƶÈ:79.4%
Journal of Asian Natural Products Research          2008          10          299-302
A new lignan glycoside from the rhizomes of Imperata cylindrica
Dae-Young Lee, Kyung-Min Han, Myoung-Chong Song, Do-Gyeong Lee,Yeong-Deok Rho and Nam-in Baek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     matairesinol 4'-O-¦Â-D-apiofuranosyl(1¡ú2)-¦Â-D-glucopyranoside
C31H40O15     ÏàËƶÈ:62.5%
Chemical & Pharmaceutical Bulletin          1998          46          1044-1047
New Steroid and Matairesinol Glycosides from Safflower (Carthamus tinctorius L.) Oil Cake
Akito NAGATSU,Hui Li ZHANG,Toshihiro WATANABE,Nari TANIGUCHI,Keiichiro HATANO,Hajime MIZUKAMI and Jinsaku SAKAKIBARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     trigonotin C
C33H38O18     ÏàËƶÈ:60.6%
Journal of Natural Products          2008          71(7)          1178-1181
Identification of Sucrose Diesters of Aryldihydronaphthalene-Type Lignans from Trigonotis peduncularis and the Nature of Their Fluorescence
Hideaki Otsuka, Hidenori Kuwabara, and Hiromi Hoshiyama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     viscumneoside
    ÏàËƶÈ:58.8%
Acta Pharmaceutica Sinica          1990          Vol 25          608-611
STUDIES ON THE CHEMICAL COMPONENTS OF VISCUMCOLORATUM ¢÷. ISOLATION AND STRUCTURE OF VISCUMNEOSIDE ¢÷
DY Kong; HT Li and SQ Luo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     trigonotin A
C35H40O19     ÏàËƶÈ:57.1%
Journal of Natural Products          2008          71(7)          1178-1181
Identification of Sucrose Diesters of Aryldihydronaphthalene-Type Lignans from Trigonotis peduncularis and the Nature of Their Fluorescence
Hideaki Otsuka, Hidenori Kuwabara, and Hiromi Hoshiyama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     rupestrin C
C35H40O19     ÏàËƶÈ:57.1%
Journal of Natural Products          2006          69(4)          682-684
Lignan Oligosaccharide Esters from Eritrichium rupestre
Mao-Rong Suo, Jun-Shan Yang, and Qing-Hua Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     compounds 18
C34H42O13     ÏàËƶÈ:56.2%
Phytochemistry          2004          65          2003-2011
Constituents from the bark of Tabebuia impetiginosa
Tsutomu Warashina, Yoshimi Nagatani, Tadataka Noro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     rupestrin B
C32H36O17     ÏàËƶÈ:56.2%
Journal of Natural Products          2006          69(4)          682-684
Lignan Oligosaccharide Esters from Eritrichium rupestre
Mao-Rong Suo, Jun-Shan Yang, and Qing-Hua Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     glehlinoside D
C34H40O15     ÏàËƶÈ:55.8%
Acta Pharmaceutica Sinica          2008          Vol 43          1036-1039
A new 8-O-4' neolignan from Glehnia littoralis
WANG Li-li; KONG Wei-xue; YUAN Zhong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     salsaside E
C32H40O16     ÏàËƶÈ:53.1%
Helvetica Chimica Acta          2007          Vol. 90          79
New Glycosides from Cistanche salsa
Li Lei, Yong Jiang, Xiao-Ming Liu, Peng-Fei Tu, Li-Jun Wu, and Fa-Kui Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     agastinol
C27H28O8     ÏàËƶÈ:53.1%
Journal of Natural Products          2002          65          414-416
Agastinol and Agastenol, Novel Lignans from Agastache rugosa and Their Evaluation in an Apoptosis Inhibition Assay
Choonghwan Lee, Hyuna Kim, and Yunghee Kho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     agastenol
C27H26O8     ÏàËƶÈ:53.1%
Journal of Natural Products          2002          65          414-416
Agastinol and Agastenol, Novel Lignans from Agastache rugosa and Their Evaluation in an Apoptosis Inhibition Assay
Choonghwan Lee, Hyuna Kim, and Yunghee Kho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     9'-methoxyl rutarensin
C32H32O16     ÏàËƶÈ:53.1%
Journal of Asian Natural Products Research          2007          9          59-65
Bioactive coumarins from Boenninghausenia sessilicarpa
Q.-Y. YANG, X.-Y. TIAN and W.-S. FANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     luteolin-7-O-(6''-trans-feruloyl)-¦Â-D-glucopyranoside
    ÏàËƶÈ:53.1%
Journal of China Pharmaceutical University          2010          41          120-123
Chemical constituents from the leaves of Callicarpa nudiflora
GAO Fei-peng; WANG Hao; YE Wen-cai; ZHAO Shou-xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     matairesinol-4'-O-¦Â-gentiobioside
C32H42O16     ÏàËƶÈ:53.1%
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
16 .     glehlinoside A
C34H43O14     ÏàËƶÈ:52.9%
Chemical & Pharmaceutical Bulletin          2002          50          73-77
Constituents of the Underground Parts of Glehnia littoralis
Zhong Yuan, Yasuhiro Tezuka, Wenzhe Fan, Shigetoshi Kadota and Xian Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     Vanilloylicariside E5
C34H40O14     ÏàËƶÈ:52.9%
Archives of Pharmacal Research          2009          32          1345-1349
Lignans from the fruits of the red pepper (Capsicum annuum L.) and their antioxidant effects
Dae-Young Lee, Do-Gyeong Lee, Jin-Gyeong Cho, Myun-Ho Bang and Ha-Na Lyu, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     serratumoside A
C36H48O19     ÏàËƶÈ:52.7%
Chinese Chemical Letters          2000          11          323-326
A New Phenylpropanoid Glycoside: Serratumoside A from Clerodendrum serratum
Hui YANG, Ai Jun HOU, Shuang Xi MEI, Li Yan PENG, Han Dong SUN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     fraxisecoside
C33H40O20     ÏàËƶÈ:51.5%
Journal of Asian Natural Products Research          2008          10          205-210
Water-soluble constituents of the root barks of Fraxinus rhynchophylla (Chinese drug Qinpi)
KAI XIAO, QING-HONG SONG, SHU-WEI ZHANG and LI-JIANG XUAN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     arctigenin-4'-O-¦Â-gentiobioside
    ÏàËƶÈ:51.5%
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
21 .     glehlinoside F
C35H42O14     ÏàËƶÈ:51.4%
Chinese Chemical Letters          2008          19          1459-1461
New lignan glycosides from Glehnia littoralis
Wei Xue Kong, Zhong Yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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1 .     ginsenoside Rh1
    ÏàËƶÈ:75%
Chinese Traditional and Herbal Drugs          1996          27          647-649
Isolation and Identification of Ginsenoside from the Leaves of Wild Ginseng(Panax ginseng)
Li Jing; Wei Yongdi(Berhune Medical University; Changchun);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     1¦Â,2¦Á,3¦Â,20(R)-Tetrahydroxydammar-24-ene 3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
C42H72O13     ÏàËƶÈ:72.7%
Planta Medica          2009          75          541-543
Dammarane-Type Triterpene Glycosides from Oncoba manii Active against Methicillin-Resistant Staphylococcus aureus
Eliane Garo, Chia S. Hung, Russell B.Williams, Krista M. Olson,Jin-Feng Hu, Stephanie M. Rice, Grayson W. Hough,Matt G. Goering, Mark O'Neil-Johnson, Gary R. Eldridge,Courtney M. Starks
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     ginsenoside Rh
    ÏàËƶÈ:72.2%
Planta Medica          1982          44          146-149
Degradation of Ginseng Saponins under Mild Acidic Conditions
B. H. Han, M. H. Park, Y. N. Han, L. K. Woo, U. Sankawa, S. Yahara and 0. Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     ginsenoside-Rh1
    ÏàËƶÈ:72.2%
Chemical & Pharmaceutical Bulletin          1979          27          88-92
Further Study on Dammarane-Type Saponins of Roots, Leaves, Flower-Buds, and Fruits of Panax ginseng C. A. MEYER
SHOJI YAHARA,KIYOKO KAJI and OSAMU TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     20(S)-È˲ÎÔíÜÕ-Rh1
    ÏàËƶÈ:72.2%
Chinese Traditional and Herbal Drugs          2009          40          1204-1207
Î÷Ñó²Î×ÜÔíÜÕÒÒËáË®½â²úÎïµÄ»¯Ñ§³É·ÖÑо¿(¢ñ)
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Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     20(s)-È˲ÎÔíÜÕ-Rh1
    ÏàËƶÈ:72.2%
Chinese Pharmaceutical Journal          2000          35          82-84
Isolation and identification of 20(s)-Ginsenoside Rh_1, Rh_2 and Ginsenoside Rh_3 from the leaves of Panax quinquefolium
Cong Dengli (Cong DL), Song Changchun (Song CC), Xu Jingda (Xu JD)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     20(S)-Rh1
    ÏàËƶÈ:72.2%
Chinese Journal of Medicinal Chemistry          1992          2(2)          31-35
STUDIES ON THE CHEMICAL CONSTITUENTS OF FLOWER-BUDS OF PANAX GINSENG C A MEYER
Wang Hongyan Pei Yuping Chen Yingjie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     ginsenoside Rh1
    ÏàËƶÈ:69.4%
Chinese Chemical Letters          2001          12          59-62
A Novel Hexanordammarane Glycoside from the Roots of Panax notoginseng
Hai Zhou LI, Rong Wei TENG, Chong Ren YANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     notoginsenoside R9
C36H622O10     ÏàËƶÈ:69.4%
Phytochemistry          1996          41          1419-1422
Minor dammarane saponins from Panax notoginseng
Ping Zhao, Yu-Qing Liu, Chong-Ren Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     ginsenoside Rh1
    ÏàËƶÈ:69.4%
Phytochemistry          1996          41          1419-1422
Minor dammarane saponins from Panax notoginseng
Ping Zhao, Yu-Qing Liu, Chong-Ren Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     ginsenoside Rh1
    ÏàËƶÈ:69.4%
Journal of Natural Medicines          2006          60          135-137
New dammarane-type saponin from roots of Panax notoginseng
Nozomi Komakine, Mamoru Okasaka, Yoshihisa Takaishi, Kazuyoshi Kawazoe and Kotaro Murakami, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     20(S)-ginsenoside-Rh1
    ÏàËƶÈ:69.4%
Magnetic Resonance in Chemistry          2002          40          483-488
Complete assignment of 1H and 13C NMR data for nine protopanaxatriol glycosides
Rongwei Teng, Haizhou Li, Jiangtao Chen, Dezu Wang, Yineng He and Chongren Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     20 (R)-È˲ÎÔíÜÕ-Rh1
C36H62O9     ÏàËƶÈ:69.4%
Chinese Traditional and Herbal Drugs          2009          40          1204-1207
Î÷Ñó²Î×ÜÔíÜÕÒÒËáË®½â²úÎïµÄ»¯Ñ§³É·ÖÑо¿(¢ñ)
¼Ö¼ÌÃ÷;Íõ×ÚȨ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     ginsenoside Rh1
    ÏàËƶÈ:69.4%
Chinese Traditional and Herbal Drugs          2005          36          499-503
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Àî¹úºì,ÉòÔÂë,ÍõÆô·½,ÕÅ¿ËÇÚ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     20(S)-ginsenoside Rh1
    ÏàËƶÈ:69.4%
Chinese Pharmaceutical Journal          2008          43          412-415
Study on Isolation and Structural Elucidation of Ginsenosides from Transgenic Crown Gall of Panax quinquefolium
ZHU Jian-hua YU Rong-min YAN Chun-yan SONG Li-yan ZHAO Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound III
    ÏàËƶÈ:69.4%
Chinese Journal of Medicinal Chemistry          1992          2(2)          31-35
STUDIES ON THE CHEMICAL CONSTITUENTS OF FLOWER-BUDS OF PANAX GINSENG C A MEYER
Wang Hongyan Pei Yuping Chen Yingjie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     pisumosides B
C32H52O16     ÏàËƶÈ:66.6%
Chemical & Pharmaceutical Bulletin          2001          49(1)          73-77
Medicinal Foodstuffs. XXII.1) Structures of Oleanane-Type Triterpene Oligoglycosides, Pisumsaponins I and II, and Kaurane-Type Diterpene Oligoglycosides, Pisumosides A and B, from Green Peas, the Immature Seeds of Pisum sativum L.
Toshiyuki MURAKAMI, Kentarou KOHNO, Hisashi MATSUDA, and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     ginsenoside-Rh6
C36H62O11     ÏàËƶÈ:66.6%
Chemical & Pharmaceutical Bulletin          2001          49(4)          442-446
Six New Dammarane-type Triterpene Saponins from the Leaves of Panax ginseng
De-Qiang DOU,Ying-Jie CHEN,Li-Hong LIANG,Fa-Gen PANG,Noriko SHIMIZU, and Tadahiro TAKEDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     vina-ginsenoside-R10
C36H62O10     ÏàËƶÈ:66.6%
Chemical & Pharmaceutical Bulletin          1994          42          634-640
Saponins from Vietnamese Ginseng, Panax vietnamensis HA et GRUSHV. Collected in Central Vietnam. III
NGUYEN Minh Duc,Ryoji KASAI,Kazuhiro OHTANI,Aiko ITO,Thoi Nham NGUYEN,Kazuo YAMASAKI and Osamu TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     lyciumoside III
C32H56O13     ÏàËƶÈ:66.6%
Chemical & Pharmaceutical Bulletin          1993          41          703-709
Cyclic Peptides, Acyclic Diterpene Glycosides and Other Compounds from Lycium chinense MILL
Shoji YAHARA,Choko SHIGEYAMA,Takeshi URA,Kaori WAKAMATSU,Tadashi YASUHARA and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     ginsenoside Rh1
    ÏàËƶÈ:66.6%
Acta Pharmaceutica Sinica          1987          Vol 22          750-755
STUDIES ON THE CHEMICAL CONSTITUENTS OF PANAX QUINQUEFOLIUS LINN
XU Sui-Xu; CHEN Ying-Jie; CAI Zhong-Oin and YAO Xin-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     Ginsenoside Rh1
    ÏàËƶÈ:66.6%
Molecules          2010          15          399-406
Isolation, Synthesis and Structures of Ginsenoside Derivatives and Their Anti-Tumor Bioactivity
Mei Han, Jin-Gang Hou, Cheng-Ming Dong, Wei Li, Hao-Lun Yu, Yi-Nan Zheng and Li Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     20(R)-Rh1
    ÏàËƶÈ:66.6%
Chinese Journal of Medicinal Chemistry          1992          2(2)          31-35
STUDIES ON THE CHEMICAL CONSTITUENTS OF FLOWER-BUDS OF PANAX GINSENG C A MEYER
Wang Hongyan Pei Yuping Chen Yingjie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     È˲ÎÔíÜÕ Rh1
    ÏàËƶÈ:66.6%
Journal of Shenyang Pharmaceutical University          1992          9          217-218
STUDIES ON THE ANTIARRHYTHMIC CONSTITUENTS FROM THE RHIZOMES OF PANAX GINSENG C.A.MEYER
Zhang Yonghe Lin Jingnan Pei Yuping Chen Yingjie Liu Chongming Xu Shuixu Yao Xinsheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

»¯ºÏÎï4£º

1 .     Chrysoeriol 7-glucoside
    ÏàËƶÈ:84%
Journal of Chinese Pharmaceutical Sciences          2000          9          119-121
Flavone Glycosides from the Leaves of Ginkgo biloba
Tang Yuping, Zheng Weiping, Lou Fengchang, Li Yanfang and Wang Jinghua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     chrysoeriol-7-O-¦Â-D-glucoside
C22H22O11     ÏàËƶÈ:84%
Natural Product Sciences          2006          12          89-93
Chemical Constituents of Gomphrena globosa. II
Dinda, Biswanath; Ghosh, Biplab; Achari, Basudev; Arima, Shiho; Sato, Nariko; Harigaya, Yoshihiro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     chrysoeriol-7-O-¦Â-D-glucoside
    ÏàËƶÈ:84%
China Journal of Chinese Materia Medica          2010          35          869-871
Chemical constituents from Lagotis brevituba
CHI Feng; DENG Jun; WANG Yanhan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     ½ðÊ¥²Ý»ÆËØ-7-O-¦Â-D-ÆÏÌÑÌÇÈ©ËáÜÕ
    ÏàËƶÈ:84%
Chinese Traditional and Herbal Drugs          2009          40          1715-1719
ËÕÃŰ׾ƲݵĻ¯Ñ§³É·ÖÑо¿
½âЦè¤;ËÕÑÞ·¼;²ñÐÀ;ÖÜάÒå;µËС¾ê;¹ùÀöƼ;¸ßÐã÷;ÕŲ®Àñ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     ½ðÊ¥²ÝËØ-7-O-¦Â-D-ßÁà«ÆÏÌÑÌÇÜÕ
C22H22O11     ÏàËƶÈ:84%
Chinese Traditional and Herbal Drugs          2008          39          1635-1636+1720
»ÒձëÈ̶¬µÄ»¯Ñ§³É·ÖÑо¿
¼ÖÏþ¶«;·ëìã;ÕÔÐËÔö;ÍõÃù;ËïºÆ;¶­ÔÆ·¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     chrysoeriol-7-O-¦Â-D-g lucoside
C22H22O11     ÏàËƶÈ:84%
Chinese Traditional and Herbal Drugs          2005          36          819-820
²ØÒ©ÐÄÒ¶Íöù·çÖлÆͪ³É·ÖµÄÑо¿
ÆÕ½¨ÐÂ,ÕÔ¾²·å,ÑòÏþ¶«,Àî´äºì,ÀîÁ¼
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     chrysoeriol-7-O-¦Â-D-glucopyranoside
    ÏàËƶÈ:84%
Chinese Journal of Natural Medicines          2005          3          86-89
Acetylenes and Flavonoids from Artemisia scoparia¢ò
XIE Tao; LIU Jing; LIANG Jing-Yu; ZHANG Zhi-Ming; WEI Xiu-Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     ¿ÂÒÁÀûËØ-7-O-¦Â-D-ÆÏÌÑÌÇÜÕ
    ÏàËƶÈ:84%
Chinese Pharmaceutical Journal          2009          44          336-338
Study on Five Flavanoids in Barks of Quercus pannosa Hand.-Mazz.
LI Qin SHEN Yue-mao LI Ping~
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     chrysoeriol-7-O-¦Â-D-glucoside
    ÏàËƶÈ:84%
Chinese Pharmaceutical Journal          2009          44          1475-1477
Studies on Flavonoids from Galium aparine
CAI Xiao-mei, YANG Juan, RAO Qiong-juan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     chrysoeriol-7-O-glucoside
    ÏàËƶÈ:84%
Journal of China Pharmaceutical University          2005          36          402-404
Chemical Constituents of Dendranthema nankingense
YANG Nian-Yun; REN Ai-Nong; HU Wan-Chun; QIAN Shi-Hui; DUAN Jin-Ao; TIAN Li-Juan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     chrysoeriol-7-O-glucopyranoside
C22H22O11     ÏàËƶÈ:84%
Turkish Journal of Chemistry          2006          30          383-390
Secondary Metabolites from Phlomis syriaca and Their Antioxidant Activities
¨¹. ŞEBNEM HARPUT, İHSAN ÇALIŞ, İCLAL SARACOĞLU, ALİ ARSLAN DÖNMEZ, AKITO NAGATSU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     chrysoeriol 7-O-glucoside
    ÏàËƶÈ:84%
Chemistry & Biodiversity          2012          9          2096-2158
Flavonoids in Subtribe Centaureinae (Cass.) Dumort. (Tribe Cardueae, Asteraceae): Distribution and 13C-NMR Spectral Data
Carmen Formisano, Daniela Rigano, Felice Senatore, Svetlana Bancheva, Antonella Maggio, Sergio Rosselli and Maurizio Bruno
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     5,7,4'-Trihydroxy-3'-methoxyflavone-7-O-¦Â-D-glucopyranoside
    ÏàËƶÈ:84%
Phytochemistry Letters          2011          4          151-157
Phenolic constituents of the inflorescences of Sorbus torminalis (L.) Crantz
Monika A. Olszewska, Joanna Marta Roj
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     chrysoeriol-7-O-¦Â-D-glucoside
    ÏàËƶÈ:84%
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
15 .     thermopsoside
    ÏàËƶÈ:80%
Chemistry of Natural Compounds          1989          25          303-308
FLAVONOIDS OF Thermopsisalterniflora. CROTONOYLTHERMOPSOSIDE AND CROTONOYLCOSMOSIIN - NEW ACYLATED FLAVONE GLYCOSIDES
M. P. Yuldashev, E. Kh. Batirov, A. D. Vdovin,V. M. Malikov, and M. R. Yagudaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     chrysoerin-7-O-¦Â-D-glucoside
    ÏàËƶÈ:80%
China Journal of Chinese Materia Medica          2006          31          395-397
Studies on the flavones in of Chrozophora sabulosa
Shi Xinhong, LIU Youqiang, KONG Lingyi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     O-(6''-O-Acetyl-)-¦Â-glucopyranosylchrysoeriol
C24H24O12     ÏàËƶÈ:80%
Fitoterapia          2009          80          51-53
An iridoid and a flavonoid from Sideritis lanata L.
Kalina I. Alipieva , Emanuela P. Kostadinova , Ljuba N. Evstatieva ,Marina Stefova , Vassya S. Bankova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     chrysoeriol-7-O-¦Â-D-glucopyranoside
    ÏàËƶÈ:80%
Chinese Journal of Natural Medicines          2005          3          357-358
Chemical Constituents from Lithospermum zollingeri
ZHANG Xian-Tao; YIN Zhi-Qi; YE Wen-Cai; NI Li; ZHAO Shou-Xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     chrysoerid-7-O-¦Â-D-glucoside
    ÏàËƶÈ:80%
Chinese Pharmaceutical Journal          2005          40          1778-1780
Study on chemical constituents from Artemisia selengensis leaves
ZHANG Jian, KONG Ling-yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     crotonoylthermopsoside
C26H26O12     ÏàËƶÈ:76.9%
Chemistry of Natural Compounds          1989          25          303-308
FLAVONOIDS OF Thermopsisalterniflora. CROTONOYLTHERMOPSOSIDE AND CROTONOYLCOSMOSIIN - NEW ACYLATED FLAVONE GLYCOSIDES
M. P. Yuldashev, E. Kh. Batirov, A. D. Vdovin,V. M. Malikov, and M. R. Yagudaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     chrysoeriol 4'-O-¦Â-D-glucopyranoside
    ÏàËƶÈ:76%
Phytochemistry          2000          55          67-75
Phenolic glycosides of forage legume Onobrychis viciifolia
Yinrong Lu, Yan Sun, L. Yeap Foo, W.C. McNabb, A.L. Molan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     chrysoeriol-4'-O-glucoside
    ÏàËƶÈ:76%
China Journal of Chinese Materia Medica          2001          26          841-844
Studies on Flavonoids from Leaves of Callicarpa bodinieri Levl.
REN Fengzhi, LUAN Xianhui, ZHAO Yimin, QU Huihua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     tricin-7-O-¦Â-D-glucopyranoside
    ÏàËƶÈ:76%
China Journal of Chinese Materia Medica          1998          23          614-616
Studies on Flavonoids from Fenugreek (Trigonella foenumgraecum L.)
Shang Mingying , Cai Shaoqing , Han Jian , Li Jun , Zhao Yuying and Zheng Junhua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     Tricin 7-glucoside
    ÏàËƶÈ:76%
Records of Natural Products          2008          2          76-82
Anti-ulcerogenic Activity of Extract and Some Isolated Flavonoids from Desmostachia bipinnata (L.) Stapf
Amani S. Awaad, Nawal H. Mohamed, Derek J. Maitland and
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     Chrysoeriol-7-O-glucoside
    ÏàËƶÈ:76%
Natural Product Sciences          2007          13          186-189
Phytochemical and Biological Studies on Verbascum sinaiticum Growing in Egypt
Mahmoud, Samia M.; Abdel-Azim, Nahla S.; Shahat, Abdelaaty A.; Ismail, Shams I.; Hammouda, Faiza M.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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