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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½3561¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Notoginsenoside ST-2 C43H74O15 ÏàËÆ¶È:97.6% Journal of Agricultural and Food Chemistry 2008 56 1751-1756 Dammarane-Type Glycosides from Steamed Notoginseng Peng-Ying Liao, Dong Wang, Ying-Jun Zhang and Chong-Ren Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Notoginsenoside ST-3 C43H74O15 ÏàËÆ¶È:88.3% Journal of Agricultural and Food Chemistry 2008 56 1751-1756 Dammarane-Type Glycosides from Steamed Notoginseng Peng-Ying Liao, Dong Wang, Ying-Jun Zhang and Chong-Ren Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ginsenoside-Rg5 ÏàËÆ¶È:88.0% Chinese Chemical Letters 2000 11 909-912 Ginsenoside-Rg6, a Novel Triterpenoid Saponin from the Stem-Leaves of Panax ginseng C. A. Mey. Xiu Wei YANG, Long Yun LI- Jian Ming TIAN, Zhi Wei ZHANG, Jin Mei YE. Wei Fang Gu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ginsenoside-Rg5 ÏàËÆ¶È:88.0% Journal of Asian Natural Products Research 2004 6 289-293 ISOGINSENOSIDE-Rh3, A NEW TRITERPENOID SAPONIN FROM THE FRUITS OF PANAX GINSENG C. A. MEY JI-YAN WANG, XIANG-GAO LI, YI-NAN ZHENG and XIU WEI YANG Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ginsenoside Rg5 ÏàËÆ¶È:88.0% Archives of Pharmacal Research 1996 19 551-553 High performance liquid chromatographic assay of a new fluoroquinolone, LB20304, in the plasma of rats and dogs Mi-Kyeong Seo, Yi-Na Jeong, Hoon-Joo Kim, In-Chull Kim and Yong-Hee Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ginsenoside Rg5 ÏàËÆ¶È:88.0% Archives of Pharmacal Research 2002 25 428-432 Three new dammarane glycosides from heat processed ginseng II Ho Park, Na Young Kim, Sang Beom Han, Jong Moon Kim and Sung Won Kwon, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ginsenoside Rg5 ÏàËÆ¶È:88.0% Archives of Pharmacal Research 2002 25 837-841 Four new acetylated ginsenosides from processed ginseng (sun ginseng) Il Ho Park, Sang Beom Han, Jong Moon Kim, Longzhu Piao and Sung Won Kwon, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 10 C42H72O13 ÏàËÆ¶È:85.7% Chinese Traditional and Herbal Drugs 2009 40 1876-1879 Î÷Ñó²Î×ÜÔíÜÕÒÒËáË®½â²úÎïµÄ»¯Ñ§³É·ÖÑо¿(¢ò) Íõ×ÚȨ;¼Ö¼ÌÃ÷ Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-O-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside-12¦Â,25-dihydroxydammar-(E) 20 (22)-ene C42H72O13 ÏàËÆ¶È:83.3% Journal of China Pharmaceutical University 2011 42 115-118 Minor saponins constituents from Panax Notoginseng tap root LIU Li-min; ZHANG Xiao-qi; WANG Hao*; YE Wen-cai; ZHAO Shou-xun Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Ginsenoside Rh15 C42H70O13 ÏàËÆ¶È:83.3% Planta Medica 2012 78 189-192 Four New Dammarane-Type Triterpene Saponins from the Stems and Leaves of Panax ginseng and Their Cytotoxicity on HL-60 Cells Li, Ke-Ke; Yao, Chun-Mei; Yang, Xiu-Wei: Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ginsenoside Rs4 C44H72O13 ÏàËÆ¶È:81.8% Archives of Pharmacal Research 2002 25 837-841 Four new acetylated ginsenosides from processed ginseng (sun ginseng) Il Ho Park, Sang Beom Han, Jong Moon Kim, Longzhu Piao and Sung Won Kwon, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . floralginsenoside E C42H72O15 ÏàËÆ¶È:80.9% Chemical & Pharmaceutical Bulletin 2007 55(4) 571-576 Medicinal Flowers. XI.1) Structures of New Dammarane-Type Triterpene Diglycosides with Hydroperoxide Group from Flower Buds of Panax ginseng Masayuki YOSHIKAWA,Sachiko SUGIMOTO, Seikou NAKAMURA, and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ginsenoside Rz1 ÏàËÆ¶È:80.9% Chemical & Pharmaceutical Bulletin 2009 57 92-94 Ginsenosides from Heat Processed Ginseng Sang Myung Lee, Hyun Ju Shon, Chung-Sig Choi, Tran Manh Hung, Byung Sun Min and KiHwan Bae Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 20(S)-È˲ÎÔíÜÕ-Rg3 ÏàËÆ¶È:80.9% Chinese Traditional and Herbal Drugs 2009 40 360-363 ÒæÖǸ´·½ÌÀµÄ»¯Ñ§³É·ÖÑо¿(¢ó) ËïÁ¬ÄÈ;Àîϼ;ÑîÓ±²©;ÕÔ¹ó¾û;³ÂÍòÉú Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3-O-¦Â-D-glucopyranosyl(1¡ú 2)-glucopyransyl-3¦Â,12¦Â,20(S)-trihydroxy-25-hydroperoxydammar-3(E)-en C42H72O15 ÏàËÆ¶È:80.9% Chinese Traditional and Herbal Drugs 2009 40 1204-1207 Î÷Ñó²Î×ÜÔíÜÕÒÒËáË®½â²úÎïµÄ»¯Ñ§³É·ÖÑо¿(¢ñ) ¼Ö¼ÌÃ÷;Íõ×ÚȨ Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . centelloside B C47H78O16 ÏàËÆ¶È:80.8% Journal of Asian Natural Products Research 2011 Vol.13,No.8 749-755 Two new dammarane monodesmosides from Centella asiatica Xiao-Xiang Weng, Yan Shao, Yun-Yan Chen, Wen Gao, Liang Cheng and De-Yun Kong Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 23-O-acetyl-3¦Â,12¦Â,-23S,24¦Á-tetrahydroxy-20S,25-epoxydammarane 3-O-[¦Â-Dxylopyranosyl(1¡ú2)]-¦Â-D-glucopyranoside C43H72O15 ÏàËÆ¶È:79.0% Journal of Natural Products 2004 67 942-952 Dammarane-Type Glycosides from Gynostemma pentaphyllum Feng Yin, Lihong Hu, Fengchang Lou, and Ruixiang Pan Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Notoginsenoside SFt4 C47H76O16 ÏàËÆ¶È:78.7% Natural Products and Bioprospecting 2011 1 124-128 Dammarane-type saponins from steamed leaves of Panax Notoginseng Qing Liu, Jun-Jiang Lv, Min Xu, Dong Wang, Hong-Tao Zhu, Chong-Ren Yang, Ying-Jun Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . ginsenoside Rg3 ÏàËÆ¶È:78.5% Chinese Traditional and Herbal Drugs 2005 36 499-501 ·¢½ÍÈýÆßÖеÄÔíÜճɷÖÑо¿ Àî¹úºì,ÉòÔÂë,ÍõÆô·½,ÕÅ¿ËÇÚ Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound Vina-R13 ÏàËÆ¶È:78.5% Chinese Traditional and Herbal Drugs 2000 31 801-803 Saponins from the Fruit of Panax quinquefolius Collected in Canada Department of Natural Medicine; Norman Bethune University of Medical Sciences (Changchun )Hao Xiuhua; Li Pingya and Li Xian Research Center of New Drug; Changchun College of TCM Liu Yongqiang Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ginsenoside Rg3 ÏàËÆ¶È:78.5% Natural Product Research and Development 2006 18 549-554 A Further Investigation on the Chemical Constituents from the Leaves of Panax notoginseng LI Hai-zhou; ZHANG Ying-jun; YANG Chong-ren* Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 20(S)-Rg3 ÏàËÆ¶È:76.1% Phytochemistry 2008 69 218-224 Conversion of major ginsenoside Rb1 to 20(S)-ginsenoside Rg3 by Microbacterium sp. GS514 Le-Qin Cheng, Ju Ryun Na, Myun Ho Bang, Myung Kyum Kim, Deok-Chun Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . ginsenoside Rg3 (1a) ÏàËÆ¶È:76.1% Phytochemistry 2008 69 218-224 Conversion of major ginsenoside Rb1 to 20(S)-ginsenoside Rg3 by Microbacterium sp. GS514 Le-Qin Cheng, Ju Ryun Na, Myun Ho Bang, Myung Kyum Kim, Deok-Chun Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . gynoside A C41H70O13 ÏàËÆ¶È:76.1% Journal of Natural Products 2004 67 1147-1151 Five New Ocotillone-Type Saponins from Gynostemma pentaphyllum Xin Liu, Wencai Ye, Ziyao Mo, Biao Yu, Shouxun Zhao, Houming Wu,Chuntao Che, Renwang Jiang, Thomas C. W. Mak, and W. L. Wendy Hsiao Structure 13C NMR ̼Æ×Ä£Äâͼ |

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1 . Notoginsenoside ST-2 C43H74O15 ÏàËÆ¶È:97.6% Journal of Agricultural and Food Chemistry 2008 56 1751-1756 Dammarane-Type Glycosides from Steamed Notoginseng Peng-Ying Liao, Dong Wang, Ying-Jun Zhang and Chong-Ren Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Notoginsenoside ST-3 C43H74O15 ÏàËÆ¶È:88.3% Journal of Agricultural and Food Chemistry 2008 56 1751-1756 Dammarane-Type Glycosides from Steamed Notoginseng Peng-Ying Liao, Dong Wang, Ying-Jun Zhang and Chong-Ren Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ginsenoside-Rg5 ÏàËÆ¶È:88.0% Chinese Chemical Letters 2000 11 909-912 Ginsenoside-Rg6, a Novel Triterpenoid Saponin from the Stem-Leaves of Panax ginseng C. A. Mey. Xiu Wei YANG, Long Yun LI- Jian Ming TIAN, Zhi Wei ZHANG, Jin Mei YE. Wei Fang Gu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ginsenoside-Rg5 ÏàËÆ¶È:88.0% Journal of Asian Natural Products Research 2004 6 289-293 ISOGINSENOSIDE-Rh3, A NEW TRITERPENOID SAPONIN FROM THE FRUITS OF PANAX GINSENG C. A. MEY JI-YAN WANG, XIANG-GAO LI, YI-NAN ZHENG and XIU WEI YANG Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ginsenoside Rg5 ÏàËÆ¶È:88.0% Archives of Pharmacal Research 1996 19 551-553 High performance liquid chromatographic assay of a new fluoroquinolone, LB20304, in the plasma of rats and dogs Mi-Kyeong Seo, Yi-Na Jeong, Hoon-Joo Kim, In-Chull Kim and Yong-Hee Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ginsenoside Rg5 ÏàËÆ¶È:88.0% Archives of Pharmacal Research 2002 25 428-432 Three new dammarane glycosides from heat processed ginseng II Ho Park, Na Young Kim, Sang Beom Han, Jong Moon Kim and Sung Won Kwon, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ginsenoside Rg5 ÏàËÆ¶È:88.0% Archives of Pharmacal Research 2002 25 837-841 Four new acetylated ginsenosides from processed ginseng (sun ginseng) Il Ho Park, Sang Beom Han, Jong Moon Kim, Longzhu Piao and Sung Won Kwon, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 10 C42H72O13 ÏàËÆ¶È:85.7% Chinese Traditional and Herbal Drugs 2009 40 1876-1879 Î÷Ñó²Î×ÜÔíÜÕÒÒËáË®½â²úÎïµÄ»¯Ñ§³É·ÖÑо¿(¢ò) Íõ×ÚȨ;¼Ö¼ÌÃ÷ Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-O-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside-12¦Â,25-dihydroxydammar-(E) 20 (22)-ene C42H72O13 ÏàËÆ¶È:83.3% Journal of China Pharmaceutical University 2011 42 115-118 Minor saponins constituents from Panax Notoginseng tap root LIU Li-min; ZHANG Xiao-qi; WANG Hao*; YE Wen-cai; ZHAO Shou-xun Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Ginsenoside Rh15 C42H70O13 ÏàËÆ¶È:83.3% Planta Medica 2012 78 189-192 Four New Dammarane-Type Triterpene Saponins from the Stems and Leaves of Panax ginseng and Their Cytotoxicity on HL-60 Cells Li, Ke-Ke; Yao, Chun-Mei; Yang, Xiu-Wei: Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ginsenoside Rs4 C44H72O13 ÏàËÆ¶È:81.8% Archives of Pharmacal Research 2002 25 837-841 Four new acetylated ginsenosides from processed ginseng (sun ginseng) Il Ho Park, Sang Beom Han, Jong Moon Kim, Longzhu Piao and Sung Won Kwon, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ |
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4Â¥2013-09-02 23:55:29
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