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15.3,16.9,17.0,18.0,19.5,19.7,22.3,27.1,27.3,28.6,31.0,31.7,33.0,35.6,37.8,38.2,39.5,40.2,40.6,42.2,43.7,48.5,50.7,52.1,57.2,58.1,62.1,63.1,65.4,69.1,69.7,70.8, 71.1,71.9,72.4,72.6,73.8,73.9,74.2,75.4,76.1,76.9,77.0,78.1,78.2,78.3,78.4,79.1,79.7,91.3,95.4,103.1,104.7,104.9,105.5,110.6,151.9,176.4
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ÓñÃ×-Æ»¹û: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-11 13:26:54
pulsatilloside D
C59H96O27     ÏàËÆ¶È:88.1%
Planta Medica          2002          68          183-186
New Lupane Glycosides from Pulsatilla chinensis
Wencai Ye,Qingwen Zhang,Wendy W.L.Hsiao,Shouxun Zhao,Chun-Tao Che
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     3¦Â-[(O-¦Á-L-arabinopyranosyl-(1¡ú4)-O-¦Â-D-xylopyranosyl-(1¡ú2)-O-[¦Â-D-xylopyranosyl-(1¡ú4)]-¦Â-D-glucopyranosyl)oxy]-2¦Á-hydroxylup-20(29)-en-28-oic acid ¦Á-L-rhamnopyranosyl ester
C57H92O25     ÏàËÆ¶È:86.2%
Phytochemistry Letters          2011          4          259-266
Seven new triterpene glycosides from the pericarps of Stryphnodendron fissuratum
Akihito Yokosuka, Sachiko Kawakami, Mitsue Haraguchi, Yoshihiro Mimaki
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     ryobusaponin G
C54H86O23     ÏàËÆ¶È:86.2%
Chemical & Pharmaceutical Bulletin          2013          69          134-143
Triterpene Saponins from Clethra barbinervis and Their Hyaluronidase Inhibitory Activities
Toshihiro Murata, Atsushi Suzuki, Nagisa Mafune, Eriko Sato, Toshio Miyase, Fumihiko Yoshizaki
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     3-O-¦Â-D-glucopyranosyl-(1¡ú2)-¦Á-L-arabinopyranosyl-echinocystic acid 28-O-¦Á-L-rhamnopyranosyl-(1¡ú4)-¦Â-D-glucopyranosyl(1¡ú6)-¦Â-D-glucopyranoside
C59H96O27     ÏàËÆ¶È:84.7%
Journal of Agricultural and Food Chemistry          2001          49          5969-5974
Characterization of the Triterpene Saponins of the Roots and Rhizomes of Blue Cohosh (Caulophyllum Thalictroides)
Jin-Woo Jhoo, Shengmin Sang, Kan He, Xiaofang Cheng, Nanqun Zhu, Ruth E. Stark, Qun Yi Zheng, Robert T. Rosen, and Chi-Tang Ho
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     3¦Â-[(O-¦Â-D-glucopyranosyl-(1¡ú3)-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Á-L-arabinopyranosyl)]lup-20(29)-en-28-oic-acid 28-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranosyl ester
C59H96O26     ÏàËÆ¶È:84.7%
Planta Medica          2013          79          506-512
Lupane-Type Triterpenoidal Saponins from Pulsatilla chinensis and Their Anticomplement Activities through the Classical Pathway
Xu, Qiong-ming; Shu, Zhan; Zhu, Wei-feng; Liu, Yan-li; Li, Xiao-ran; Yang, Shi-lin:
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     23-hydroxy-3¦Â-[(O-¦Á-L-rhamnopyranosyl-(1¡ú2)-O-(¦Â-D-glucopyranosyl-(1¡ú4))-¦Á-L-arabinopyranosyl)]lup-20(29)-en-28-oic acid 28-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranosyl ester
C59H96O27     ÏàËÆ¶È:83.0%
Planta Medica          2013          79          506-512
Lupane-Type Triterpenoidal Saponins from Pulsatilla chinensis and Their Anticomplement Activities through the Classical Pathway
Xu, Qiong-ming; Shu, Zhan; Zhu, Wei-feng; Liu, Yan-li; Li, Xiao-ran; Yang, Shi-lin:
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     anemoside B4
    ÏàËÆ¶È:81.3%
Chinese Traditional Patent Medicine          2002          24          293-296
Study on constituents in sediment of Decoction Pulsatilla
ZHU Hau-xu, DING Lin-sheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     3-epi-betulinic acid 3-O-¦Â-D-6'-acetylglucopyranoside 28-[¦Á-L-rhamnopyranosyl(1¡ú4)-O-¦Â-D-glucopyranosyl(1¡ú6)]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:81.0%
Journal of Natural Products          1992          Vol 55          503
An Acetylated Bidesmosidic Saponin from Schefflera octophylla
Tran Van Sung, G¨¹nter Adam
2Â¥2015-06-11 09:02:40
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