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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 14.70,16.06,17.12, 17.77, 19.00,20.42,28.52, 29.07,29.85,31.02, 31.56, 36.42,36.83,37.70,41.13,49.61,55.81,60.09,61.83,65.88,65.96,68.01,69.35,70.49,70.61, 71.91, 73.28,74.52,75.59,76.23,76.45, 76.55,79.79,80.23, 97.97,100.14,103.67,108.45,121.33,140.31 |
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ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
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xieliting(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+15 2015-06-07 11:09:26
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xieliting(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+15 2015-06-07 11:09:26
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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:86.6% 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 . paris saponin V ÏàËÆ¶È:85% Chinese Traditional and Herbal Drugs 2013 44 2808-2811 Studies on chemical constituents in roots and rhizomes of Trillium tschonoskii (II) ZHANG Zhong-li, ZUO Yue-ming, CAI Miao-ting, WANG Yan-yan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . diosgenin 3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucuroniduronic acid methyl ester ÏàËÆ¶È:80% Zeitschrift f¨¹r Naturforschung C 2006 61 171-176 Diosgenin Glucuronides from Solanum lyratum and their Cytotoxicity against Tumor Cell Lines L.-X. Sun, W.-W. Fu, W. Li, K.-S. Bi, and M.-W. Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . dioscin ÏàËÆ¶È:80% 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 5 . 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:79.5% 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 6 . diosgenin3-O-¦Á-L-rhamnopyranosyl-(1¡ú4)-[¦Á-L-arabinopyranosyl-(1¡ú2)]-¦Â-D-glucopyranoside ÏàËÆ¶È:79.5% 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 7 . diosgenin3-O-¦Â-D-glucopyranosyl-(1¡ú3)-[¦Á-L-rhamnopyranosyl-(1¡ú2)]-¦Â-D-glucopyranoside ÏàËÆ¶È:78.0% 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 8 . diosgenin 3-O-[¦Á-L-pyranrhamnose(1¡ú2)][¦Â-D-pyranxylose(1¡ú3)]-¦Â-D-pyranglycoside C44H70O16 ÏàËÆ¶È:78.0% Northwest Pharmaceutical Journal 2013 28 562-565 Studies on the chemical constituents of the flowers of Ophiopogon japonicus ZHANG Jinghua, REN Lu, MA Yufang, BAO He, ZHAO Guilan, JING Hang, WANG Junxian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . dioscin C45H72O16 ÏàËÆ¶È:77.7% Journal of Chinese Medicinal Materials 2011 34 720-723 Studies on the Chemical Constituents from the Flowers of Ophiopogon japonicus ZHU Yu-hong, ZHAO Min, REN Lu, TIAN Di, DOU Fang, WANG Jun-xian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . diosgenin 3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranosiduronic acid ÏàËÆ¶È:77.5% Zeitschrift f¨¹r Naturforschung C 2006 61 171-176 Diosgenin Glucuronides from Solanum lyratum and their Cytotoxicity against Tumor Cell Lines L.-X. Sun, W.-W. Fu, W. Li, K.-S. Bi, and M.-W. Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 10 C45H72O16 ÏàËÆ¶È:75.6% Chinese Chemical Letters 2007 18 769-772 Synthesis and antitumor activity of a group of diosgenyl glycosides Shu Jie Hou, Chuan Chun Zou, Liang Zhou, Peng Xu,De Quan Yu, Ping Sheng Lei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . diosgenin-3-O-¦Á-L-rhamnopyranosyl(1¡ú2)[¦Â-D-glucopyranoside(1¡ú3)]-¦Â-D-glucopyranoside ÏàËÆ¶È:75.5% 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, and Zhao Ding Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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