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13C NMR (101 MHz, ) ¦Ä   41.23, 57.13, 68.36, 70.80,72.40, 72.43, 76.03, 76.31, 78.90, 79.43, 79.75, 103.96, 107.10, 114.69, 116.86, 118.45, 122.80, 135.71, 139.60, 147.65
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dwblsj: ½ð±Ò+6, ¡ïÓаïÖú 2013-11-19 08:36:11
²éѯ½á¹û£º¹²²éµ½172¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     4-allyl-2-methoxyphenyl 1-O-¦Â-D-apiofuranosyl-(1-6)-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:70%
Journal of Shenyang Pharmaceutical University          2012          29          109-125
Isolation and identification of chemical constituents in the lipid-lowering fraction of Flos Helichrysum arenarium(¢ò)
WANG Li-bo; LIU Feng-zhi; GAN Chun-li; DONG Nai-wei; HOU Yun-long; WANG Ce
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     eugenyl ¦Â-rutinoside
    ÏàËÆ¶È:68.1%
China Journal of Chinese Materia Medica          2010          35          1432-1434
Chemical constituents from leaves of Boehmeria nivea
LIU Chuang; ZOU Kun; GUO Zhiyong; ZHAO Yuying; CHENG Fan; ZHANG Hongqi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     eugenyl-¦Â-rutinoside
    ÏàËÆ¶È:68.1%
Journal of Chinese Medicinal Materials          2012          35          1778-1781
Study on the Chemical Constituents in Pouzolzia zeylanica
FU Ming, NIU You-ya, YU Juan, KONG Qing-tong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     eugenyl-O-¦Â-apiofuranosyl( l''-6')-O-¦Â-glucopyranoside
C22H30O11     ÏàËÆ¶È:66.6%
Phytochemistry          1998          49          787-791
Iridoid and eugenol glycosides from Nepeta cadmea
Yoshio Taked¦Á, Yasushi Ooiso, Toshiya Masud¦Á, Gisho Hond¦Á, Hideaki Otsuk¦Á, Ekrem Sezik, Erdem Yesilada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     eugenyl O-¦Â-apiofuranosyl (1''¡ú6')-O-¦Â-glucopyranoside
    ÏàËÆ¶È:66.6%
Asian Journal of Traditional Medicines          2010          5          138-144
Chemical constituents from the Roots of Rhodiola algida var. tangutica
Min Zhang, Yueping Ma and Zhong Yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     eugenyl O-¦Â-D-glucopyranoside(Citrusin C)
    ÏàËÆ¶È:65%
Phytochemistry          1992          31          3265-3267
Perilloside a, a monoterpene glucoside from Perilla frutescens
Tomoyuki Fujita, Mitsuru Nakayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Citrusin C
    ÏàËÆ¶È:65%
Natural Product Research and Development          2011          23          999-1001
Chemical Constituents from the Aerial Parts of Inula japonica Thunb.
QIN, Jiang-jiang, ZHU, Jia-xian, ZHU, Yan, YAN, Lan, JIN, Hui-zi, ZHANG, Wei-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     3-hydroxyestragole-¦Â-D-glucopyranoside
    ÏàËÆ¶È:65%
China Journal of Chinese Materia Medica          2011          36          1779-1781
Polar constituents ofMosla Chinensis
SH, EN, Juanjuan, ZHANG, Dongming, LIU, Hua, LUO, Yongming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     4-O-¦Â-D-glucopyranosyl(1¡ú6)-¦Â-D-glucopyranosyl eugenol
C22H32O12     ÏàËÆ¶È:63.6%
Shoyakugaku Zasshi          1990          44          331-334
Studies on the Constituents of the Water Soluble Portion in Asiasari Radix
YAHARA SHOJI, KATO KIMIYO, NOHARA TOSHIHIRO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Eugenyl 4''-O-acetyl-¦Â-rutinoside
C24H34O12     ÏàËÆ¶È:62.5%
Fitoterapia          2011          82          1309-1312
Two new polyols and a new phenylpropanoid glycoside from the basidiomycete Lactarius deliciosus
Zhong-Yu Zhou, Jian-Wen Tan, Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-11-15 22:30:49
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