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huadong1227: ½ð±Ò+5, ¡ïÓаïÖú 2014-09-26 17:05:30
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huadong1227: ½ð±Ò+5, ¡ïÓаïÖú 2014-09-26 17:05:30
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²éѯ½á¹û£º¹²²éµ½281¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . Clematomandshurica saponin F C77H126O39 ÏàËÆ¶È:71.4% Planta Medica 2013 79 987-994 Triterpene Saponins from Clematis mandshurica and Their Antiproliferative Activity Gong, Yi-xia; Hua, Hui-ming; Xu, Yong-nan; Liu, Jian-yu; Yu, Zong-gui; Ma, Jing; Zhang, Hui; Jing, Yong-kui: Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . clematomandshurica saponin C C76H124O39 ÏàËÆ¶È:70.1% Journal of Natural Products 2006 69 1591-1595 Triterpene Saponins from Clematis mandshurica Shepo Shi, Dan Jiang, Caixia Dong, and Pengfei Tu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Clematomandshurica saponin H C76H124O39 ÏàËÆ¶È:70.1% Planta Medica 2013 79 987-994 Triterpene Saponins from Clematis mandshurica and Their Antiproliferative Activity Gong, Yi-xia; Hua, Hui-ming; Xu, Yong-nan; Liu, Jian-yu; Yu, Zong-gui; Ma, Jing; Zhang, Hui; Jing, Yong-kui: Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 3¦Â-[(O-¦Â-D-ribopyranosyl-(1¡ú3)-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-[¦Â-D-glucopyranosyl-(1¡ú4)]-¦Á-L-arabinopyranosyl)oxy]olean-12-en-28-oic acid O-¦Â-D-glucopyranosyl-(1¡ú3)-O-¦Á-L-rhamnopyranosyl-(1¡ú4)-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranosyl ester C76H124O39 ÏàËÆ¶È:68.8% Chemical & Pharmaceutical Bulletin 2009 57 1425-1430 Triterpene Glycosides from the Whole Plant of Anemone hupehensis var. japonica and Their Cytotoxic Activity Akihito Yokosuka, Tomoe Sano, Ken Hashimoto, Hiroshi Sakagami and Yoshihiro Mimaki Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . acacic acid ÏàËÆ¶È:68.8% Bulletin of the Chemical Society of Japan 1995 68 3483-3490 Three New Triterpenoidal Saponins Acylated with Monoterpenic Acid from Albizziae Cortex Tsuyoshi Ikeda, Satoko Fujiwara, Junei Kinjo, Toshihiro Nohara, Yoshiteru Ida, Junzo Shoji, Tetsuro Shingu, Ryuichi Isobe, Tetsuya Kajimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Oleanolic acid 3-O-¦Â-D-glucopyranosyl(1¡ú3)-¦Á-L-rhamnopyranosyl(1¡ú2)[¦Á-L-rhamnopyranosyl(1¡ú6)-¦Â-D-glucopyranosyl(1¡ú4)]-¦Á-L-arabinopyranosyl-28-O-¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl(1¡ú6)-¦Â-D-glucopyranosyl ester ÏàËÆ¶È:68.8% Molecules 2012 17 5520-5531 Saponins with Neuroprotective Effects from the Roots of Pulsatilla cernua Jian-Yu Liu, Ying-Li Guan, Li-Bo Zou, Yi-Xia Gong, Hui-Ming Hua, Yong-Nan Xu, Hui Zhang, Zong-Gui Yu and Wen-Hao Fan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . borivilianoside E C73H120O39 ÏàËÆ¶È:67.5% Journal of Natural Products 2009 72 177-181 Cytotoxic Spirostane-Type Saponins from the Roots of Chlorophytum boriWilianum Debabrata Acharya,Anne-Claire Mitaine-Offer, Nutan Kaushik, Tomofumi Miyamoto, Thomas Paululat,Jean-Franc¸ois Mirjolet, Olivier Duchamp, and Marie-Aleth Lacaille-Dubois Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound 14 ÏàËÆ¶È:67.5% Chemistry of Natural Compounds 2006 42 49-54 TRITERPENE GLYCOSIDES FROM Kalopanax septemlobum.VI. GLYCOSIDES FROM LEAVES OF Kalopanax septemlobum VAR. typicum INTRODUCED TO CRIMEA D. A. Panov, V. I. Grishkovets, V. V. Kachala, and A. S. Shashkov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . Oleanolic acid 3-O-¦Â-D-glucopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl(1¡ú3)-¦Á-L-rhamnopyranosyl(1¡ú2)[¦Â-D-glucopyranosyl(1¡ú4)]-¦Á-L-arabinopyranosyl-28-O-¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl(1¡ú6)-¦Â-D-glucopyranosyl ester C77H126O40 ÏàËÆ¶È:67.5% Molecules 2012 17 5520-5531 Saponins with Neuroprotective Effects from the Roots of Pulsatilla cernua Jian-Yu Liu, Ying-Li Guan, Li-Bo Zou, Yi-Xia Gong, Hui-Ming Hua, Yong-Nan Xu, Hui Zhang, Zong-Gui Yu and Wen-Hao Fan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . pulsatilloside F C77H126O41 ÏàËÆ¶È:67.5% Chemical & Pharmaceutical Bulletin 2013 24 471-476 Triterpenoid Saponins of Pulsatilla koreana Root Have Inhibition Effects of Tumor Necrosis Factor-¦Á Secretion in Lipopolysaccharide-Induced RAW264.7 Cells Wei Li, Yan Ding, Ya Nan Sun, Xi Tao Yan, Seo Young Yang, Chun Whan Choi, Ji Yun Cha, Young Mi Lee, Young Ho Kim Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . compound A ÏàËÆ¶È:67.5% Journal of Peking University (Health Sciences) 2004 36 421-425 Isolation and identification of chemical constituents from Albizia julibrissin Durazz ZHENG Lu; WU Gang; WANG Bin; WU Li jun; ZHAO Yu ying Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . Prosapogenin-10 ÏàËÆ¶È:67.5% Journal of Peking University (Health Sciences) 2004 36 421-425 Isolation and identification of chemical constituents from Albizia julibrissin Durazz ZHENG Lu; WU Gang; WANG Bin; WU Li jun; ZHAO Yu ying Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . borivilianoside F C73H118O39 ÏàËÆ¶È:66.2% Journal of Natural Products 2009 72 177-181 Cytotoxic Spirostane-Type Saponins from the Roots of Chlorophytum boriWilianum Debabrata Acharya,Anne-Claire Mitaine-Offer, Nutan Kaushik, Tomofumi Miyamoto, Thomas Paululat,Jean-Franc¸ois Mirjolet, Olivier Duchamp, and Marie-Aleth Lacaille-Dubois Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . contortisilioside E C75H112O40 ÏàËÆ¶È:66.2% Helvetica Chimica Acta 2004 Vol. 87 851 Contortisiliosides A-G: Isolation of Seven New Triterpene Bisdesmosides from Enterolobium contortisiliquum and Their Cytotoxic Activity Yoshihiro Mimaki, Hiroshi Harada, Chiseko Sakuma, Mitsue Haraguchi, Satoru Yui, Tomoya Kudo, Masatoshi Yamazaki, and Yutaka Sashida Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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