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1 .     2R*,3S*-toxol-7-O-¦Â-D-glucopyranoside
C19H24O9     ÏàËÆ¶È:57.8%
Phytochemistry Letters          2011          4          377-379
An amorphane sesquiterpene and a benzofuran glucoside from Eupatorium coelestinum
Dan Thi Thuy Hang, Tran Thi Hong Hanh, Chau Van Minh, Phan Van Kiem, Tran Huy Thai, Dongho Lee, Nguyen Tien Dat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     ¦Â-D-glucopyranosyl indole-3-carboxylic acid
    ÏàËÆ¶È:57.8%
Chinese Joumal of Experimental Traditional Medical Fomulae          2010          16          56-59
Studies on Chemical constituents of Mosla chinensis 'jiangxiangru'
LIU Hua, ZHANG Dong-ming, LUO Yong-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     swertiamarin
    ÏàËÆ¶È:52.6%
Helvetica Chimica Acta          2006          Vol. 89          94
Secoiridoid Glycosides from Swertia mileensis
Yan Zhou, Ying-Tong Di, Suolang Gesang, Shu-Lin Peng, and Li-Sheng Ding
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     1-galloyl-¦Â-D-glucopyranosyl-(1¡ú4)-¦Â-D-galactopyranoside
C19H26O15     ÏàËÆ¶È:52.6%
Planta Medica          2004          70          841-846
Phenolic Compounds from Baseonema acuminatum Leaves: Isolation and Antimicrobial Activity
Marinella De Leo,Alessandra Braca, Nunziatina De Tommasi,Ivan Norscia, Ivano Morelli,Lucia Battinelli, Gabriela Mazzanti,
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     swertiamarin
    ÏàËÆ¶È:52.6%
Acta Botanica Yunnanica          1993          15(1)          97-100
THE SECOIRIDOIDS ISOLATED FROM SWERTIA PUNICEA
LUO Yue-Hua, NIE Rui-Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     swertiamarin
    ÏàËÆ¶È:52.6%
Acta Pharmaceutica Sinica          1992          27          125-129
Study on iridoid glycosides from Swertia angustifolia
YH Luo and RL Nie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     indican
    ÏàËÆ¶È:52.6%
Phytochemistry          1992          31          2695-2697
Biosynthesis of indigo precursors in higher plants
Zhi-Qiang Xia, Meinhart H. Zenk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     hydracyanoside F
C17H21NO9     ÏàËÆ¶È:52.6%
Heterocycles          2010          81          909-916
New Cyanoglycosides, Hydracyanosides D, E, and F, from the Leaves of Hydrangea macrophylla
Zhibin Wang, Seikou Nakamura, Hisashi Matsuda, Lijun Wu, and Masayuki Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     ¸ùÆ¤ËØ4'-O-ÆÏÌÑÌÇÜÕ
    ÏàËÆ¶È:52.6%
Chinese Traditional and Herbal Drugs          2005          36          21-23
ÑòõÜõÀÙÖеĶþÇâ²é¶úͪ
ÍõËØ¾ê,ÑîÓÀ´º,ʯ½¨¹¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     swertiamarin
    ÏàËÆ¶È:52.6%
Chinese Traditional and Herbal Drugs          2004          35          847-849
Glycoside constituents from Swertia franchetia na
WANG Shi-sheng; XU Qing; XIAO Hong-bin; LIU Xiu-mei; DU Yu-guang; HAN Xiu-wen; LIANG Xin-miao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     swertiamarin
    ÏàËÆ¶È:52.6%
Chinese Traditional and Herbal Drugs          1995          26          7-10
Studies on the Glucoside Constituents of Shengengzhangyacai (Swertia elongata)
Kong Deyun; Jiang Yi; Yao Ying; et al(Address:Kong Deyun; shanghai Institute of Pharmaceutical Industry; Shanghai);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     trilobatin
C22H24O10     ÏàËÆ¶È:52.6%
Acta Botanica Yunnanica          2010          32          455-462
A New Lignan from Elaeagnus lanceolata (Elaeagnaceae)
SONG We i-Wu, LIBo, LIU Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     phlorizin
C21H24O10     ÏàËÆ¶È:52.6%
Chinese Journal of Medicinal Chemistry          2011          21          220-225
Chemical constituents from dried fruits of Rubus chingii
XIAO Hong-ming, ZU Ling-bo, LI Shi-ping, WANG Kai-jin, LI Ning*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     phenolic glucoside 4-[4'-O-(2',3',5 ',6'-tetrahydroxyphenyl)-¦Â-D-glucoside]-1-butene
C16H22O10     ÏàËÆ¶È:52.6%
Chinese Journal of Chemistry          2003          21          1501-1505
Triterpenoid Saponins from Luculia pincia Hook
Wen-Yi Kang, Jun-Song Wang, Xiao-Sheng Yang and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     indican
    ÏàËÆ¶È:52.6%
Heterocycles          2001          54          957-966
Chemical Constituents of Two Oriental Orchids, Calanthe discolor and C. liukiuensis: Precursor Indole Glycoside of Tryptanthrin and Indirubin
Toshiyuki Murakami, Akinobu Kishi, Tetsuo Sakurama, Hisashi Matsuda, and Masayuki Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     bruceolline K
C19H23NO7     ÏàËÆ¶È:52.6%
Journal of Natural Products          2011          74          2438-2445
Indole Alkaloids and Quassinoids from the Stems of Brucea mollis
Hui Chen, Jian Bai, Zhen-Feng Fang, Shi-Shan Yu, Shuang-Gang Ma, Song Xu, Yong Li, Jing Qu, Jin-Hong Ren, Li Li, Yi-Kang Si, and Xiao-Guang Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     phloridzin
    ÏàËÆ¶È:52.6%
Journal of Ethnopharmacology          2008          117          249-256
Anti-HIV-1 activities of compounds isolated from the medicinal plant Rhus chinensis
Rui-Rui Wang, Qiong Gu, Yun-Hua Wang, Xue-Mei Zhang, Liu-Meng Yang, Jun Zhou, Ji-Jun Chen, Yong-Tang Zheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     phloridzin
    ÏàËÆ¶È:52.6%
Journal of Chinese Medicinal Materials          2014          37          437-440
Chemical Constituents of Fortunella margarita Fruits
GE Yong-bin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     phlorizin
    ÏàËÆ¶È:52.6%
Journal of the Korean Society for Applied Biological Chemistry          2013          56          547-552
Isolation and Identification of ¦Á-Glucosidase Inhibitors from the Stem Bark of the Nutgall Tree (Rhus javanica Linn¨¦)
Jeong-Yong Cho, Kang-Deok Lee, Sun-Young Park, Won Chul Jeong, Jae-Hak Moon, Kyung-Sik Ham
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     2-(4-chloro-3-(trifluoromethyl)phenylamino)-5-(2R,3S-O-isopropylidene-4S-O-allyl-tetrahydrofuro-2,3,4-triol-5S)-1,3,4-thiadiazole
C19H19ClF3N3O4S     ÏàËÆ¶È:52.6%
Molecules          2014          19          7832-7849
Design, Synthesis and Bioactivity of Novel Glycosylthiadiazole Derivatives
Guanghui Zong, Hanqing Zhao, Rui Jiang, Jianjun Zhang, Xiaomei Liang, Baoju Li, Yanxia Shi and Daoquan Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     neohistelosamide
C21H27N3O8     ÏàËÆ¶È:52.3%
Journal of Natural Products          2002          65          649-655
Investigation of Pictet-Spengler Type Reactions of Secologanin with Histamine and Its Benzyl Derivative
Gyula Beke, L¨¢szl¨® F. Szab¨®, and Benjamin Pod¨¢nyi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     phloridzosid
    ÏàËÆ¶È:52.3%
Phytochemistry          2000          54          871-874
A stilbene and dihydrochalcones with radical scavenging activities from Loiseleuria procumbens
Muriel Cuendet, Olivier Potterat, Aline Salvi, Bernard Testa, Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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