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xielitingгæ (ÖøÃûдÊÖ)
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[ÇóÖú]
̼Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
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13C NMR (126 MHz, DMSO) ¦Ä 14.68,16.04,17.11,17.76,18.99, 20.41,28.50,29.06,29.83,31.00,31.54, 36.40,36.82,37.69,39.01, 39.17,39.34,39.51,39.67,39.84, 40.01,41.12,49.60, 55.79,60.08,61.82,65.87,65.94,68.00, 69.33,70.48,70.59,71.90,73.27,74.50,75.58, 76.21,76.43,76.53, 79.77,80.22, 97.95, 100.12,103.66, 108.44, 121.32,140.30 |
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yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
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2Â¥2015-06-04 08:13:22
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
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xieliting: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-04 08:58:30
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
xieliting: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-04 08:58:30
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1 . 25R¡÷5-spirostan-3¦Â-ol 3-O-{¦Á-L-rhamnopyranosyl(1¡ú2)-[¦Â-D-glucopyranosyl(1¡ú4)]-O-¦Â-D-galactopyranoside} C42H76O19 ÏàËÆ¶È:87.2% Journal of Agricultural and Food Chemistry 1999 47 3193-3196 Structure of Steroidal Saponins from Underground Parts of Allium nutans L. L. S. Akhov, M. M. Musienko, S. Piacente, C. Pizza, and W. Oleszek Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . dioscin ÏàËÆ¶È:80.8% Food Chemistry 2012 134 1146-1148 Dioscin: A synergistic tyrosinase inhibitor from the roots of Smilax china Chun Liang, Ju-Hwan Lim , Seung-Hyung Kim , Dong-Seon Kim Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . ophiopogonin Q C46H72O17 ÏàËÆ¶È:78.7% Steroids 2013 78 1-7 Cytotoxic steroidal saponins from Ophiopogon japonicus Ning Li, Liang Zhang, Ke-Wu Zeng, Yuan Zhou, Jia-Yu Zhang, Yan-Yun Che, Peng-Fei Tu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . ÊíÝ÷ÔíÜÕÔª-3-O-¦Á-L-ÊóÀîßÁà«ÌÇ(1¡ú2)-[¦Á-L-°¢À²®ß»à«ÌÇ(1¡ú4)]-¦Â-D-ÆÏÌÑßÁà«ÌÇÜÕ C44H70O16 ÏàËÆ¶È:78.7% Journal of Chinese Medicinal Materials 2011 34 389-392 Studies on the Chemical Constituents of Paris bashanensis ZHANG Zhi-gang, ZHAO De, DENG Jun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . diosgenin3-O-¦Á-L-rhamnopyranosyl-(1¡ú4)-[¦Á-L-arabinopyranosyl-(1¡ú2)]-¦Â-D-glucopyranoside ÏàËÆ¶È:78.7% West China Journal of Pharmaceutical Sciences 2010 25 508-511 Isolation and identification of steroidal saponins of Paris polyphylla Smith var. pseudothibetica LIU Xian-bo, ZHANG Hao, YONG Zheng-ping, XUE Dan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . diosgenin-3-O-[¦Á-L-rha(1-3)-¦Á-L-rha(1-4)-¦Á-L-rha(1-4)]-¦Â-D-glucopyranoside ÏàËÆ¶È:78.4% Chinese Joumal of Experimental Traditional Medical Fomulae 2011 17 92-96 Studies on Steroidal Saponins from Smilax china and Their Cytotoxic Activities XU Yan, WANG Hai-yan, JIANG Jia-yue, XIANG Wei, LI Man-man, LIANG Jing-yu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . coreajaponin A C50H83O22 ÏàËÆ¶È:78% Bioorganic & Medicinal Chemistry Letters 2011 21 2075-2078 Furostanol saponins from the rhizomes of Dioscorea japonica and their effects on NGF induction Ki Hyun Kim , Min Ah Kim, Eunjung Moon, Sun Yeou Kim, Sang Zin Choi ,Mi Won Son , Kang Ro Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . diosgenin-3-O-¦Á-L-rhamnopyranosyl(1¡ú2)[¦Â-D-glucopyranoside(1¡ú3)]-¦Â-D-glucopyranoside ÏàËÆ¶È:76.5% Chemistry of Natural Compounds 2007 43 672-677 SEPARATION AND IDENTIFICATION OF STEROIDAL COMPOUNDS WITH CYTOTOXIC ACTIVITY AGAINST HUMAN GASTRIC CANCER CELL LINES IN VITRO FROM THE RHIZOMES OF Paris polyphylla VAR. chinensis Huang Yun, Cui Lijian, Zhan Wenhong Dou Yuhong,Wang Yongli, Wang Qiang |
3Â¥2015-06-04 08:13:40
xieliting
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4Â¥2015-06-04 08:59:21














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