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ë®´ú¼×´¼£º ¦Ä C (126 MHz, cd3od) 14.90, 15.38, 15.92, 16.60, 17.86, 21.48, 22.83, 24.52, 25.82, 25.85, 27.05, 29.62, 30.25, 34.48, 35.26, 36.51, 38.89, 39.20, 39.59, 47.11, 47.28, 47.45, 47.62, 47.79, 47.97, 48.14, 49.65, 51.11, 51.70, 56.12, 61.10, 61.37, 61.70, 69.77, 70.10, 70.49, 73.93, 74.88, 76.26, 76.47, 76.80, 76.89, 77.05, 79.65, 83.53, 96.84, 89.94, 103.05, 103.99, 124.43, 130.89 . |
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²éѯ½á¹û£º¹²²éµ½2800¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ginsenoside Rb3 ÏàËÆ¶È:77.3% Lishizhen Medicine and Materia Medica Research 2009 20 647-650 Studies on the Chemical Constituents of YIZHI Composite Decoction(¢ò) SUN Lian-na; LI Xia; YANG Ying-bo; ZHANG Han-ming; CHEN Wan-sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Notoginsenoside E ÏàËÆ¶È:76.4% Journal of Yunnan University 2007 29 287-290 Studies on chemical constituents from Rhizomes of Panax Notoginseng (II) SONG Jian-ping, ZENG Jiang, CUI Xiu-ming, DAI Yun, JIANG Zhi-yong, ZHANG Xue-mei, ZHOU Jia-ming, MA Yun-bao, CHEN Ji-jun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . malonyl-gindenoside Rc ÏàËÆ¶È:75% Chinese Journal of Analytical Chemistry 2005 33 1783-1786 Isola tion and Identif ica tion of Two Ma lonyl-ginsenosides from the Fresh Root of Panax G inseng Sun Guangzhi, L iu Zhi, L i Xianggao, Zheng Yinan, Wang J iyan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . ginsenoside Rb2 ÏàËÆ¶È:73.5% Lishizhen Medicine and Materia Medica Research 2009 20 647-650 Studies on the Chemical Constituents of YIZHI Composite Decoction(¢ò) SUN Lian-na; LI Xia; YANG Ying-bo; ZHANG Han-ming; CHEN Wan-sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . ginsenoside Rb2 ÏàËÆ¶È:73.5% Journal of Chinese Medicinal Materials 2014 37 1387-1390 Chemical Constituents from the Fruits of Panax ginseng SUN Yan-jun, CHEN Hui, HAO Zhi-you, WANG Jun-min, ZHANG Yan-li, ZHAO Xuan, ZHENG Yi-nan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . ginsenoside-Rb2 ÏàËÆ¶È:71.6% Chemical & Pharmaceutical Bulletin 1982 30 2393-2398 Studies on the Saponins of Ginseng. IV. On the Structure and Enzymatic Hydrolysis of Ginsenoside-Ra1 HARUYO KOIZUMI,SHUICHI SANADA,YOSHITERU IDA and JUNZO SHOJI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . ginsenosides-Rb3 ÏàËÆ¶È:71.6% Natural Product Research and Development 1991 3(4) 24-30 STUDIES ON SAPONINS FROM FLOWER-BUDS OF SANCHI (PANAX NOTOGINSENG (BURK) F.H.CHEN) Zuo Guoying Wei Junxian Du Yuanchong Cao Shuming Chen Yegao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ginsenoside Rc ÏàËÆ¶È:71.6% Lishizhen Medicine and Materia Medica Research 2009 20 647-650 Studies on the Chemical Constituents of YIZHI Composite Decoction(¢ò) SUN Lian-na; LI Xia; YANG Ying-bo; ZHANG Han-ming; CHEN Wan-sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . ginsenoside Rc ÏàËÆ¶È:71.6% Journal of Chinese Medicinal Materials 2014 37 1387-1390 Chemical Constituents from the Fruits of Panax ginseng SUN Yan-jun, CHEN Hui, HAO Zhi-you, WANG Jun-min, ZHANG Yan-li, ZHAO Xuan, ZHENG Yi-nan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . malonyl-ginsenoside Rb2 ÏàËÆ¶È:71.4% Chinese Journal of Analytical Chemistry 2005 33 1783-1786 Isola tion and Identif ica tion of Two Ma lonyl-ginsenosides from the Fresh Root of Panax G inseng Sun Guangzhi, L iu Zhi, L i Xianggao, Zheng Yinan, Wang J iyan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . notoginsenoside Fe ÏàËÆ¶È:70.5% Journal of Chinese Pharmaceutical Sciences 2006 15 6-9 Enzymatic Transformation of Notoginsenoside Fe by ¦Â-Glucanase JIANG Bin-hui; ZHAO Yu-qing; HAN Ying; CUI Yu; and HU Xiao-min Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . ginsenoside Rd ÏàËÆ¶È:70.5% Lishizhen Medicine and Materia Medica Research 2009 20 647-650 Studies on the Chemical Constituents of YIZHI Composite Decoction(¢ò) SUN Lian-na; LI Xia; YANG Ying-bo; ZHANG Han-ming; CHEN Wan-sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . ÈýÆßÔíÜÕ-Fe ÏàËÆ¶È:70.5% Journal of Chinese Medicinal Materials 2004 27 489-491 Isolation and Identification of Minor Bioactive Saponinsfrom the Leaves of Panax notoginseng Jiang Binhui, Wang Chengzhi, Han Ying, Hu Xiaomin, Zheng Longxi, Zhao Yuqing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . escin IVh C53H84O23 ÏàËÆ¶È:69.8% Chemical & Pharmaceutical Bulletin 2001 49(5) 626-628 Three New Triterpene Saponins from the Seeds of Aesculus chinensis Jing ZHAO,Xiu-Wei YANG, and Masao HATTORI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . escin IVh C53H84O23 ÏàËÆ¶È:69.8% Chinese Chemical Letters 1999 10 1031-1034 Three New Triterpenoid Saponins from the Seeds of Aesculus chinensis Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . pseudo-ginsenoside-RC1 ÏàËÆ¶È:68.6% Chemical & Pharmaceutical Bulletin 1986 34 730-738 Saponins of Plants of Panax Species Collected in Central Nepal and Their Chemotaxonomical Significance. I TSUNEO NAMBA,KATSUMICHI MATSUSHIGE,TOSHINOBU MORITA and OSAMU TANAKA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 3¦Â,20S-dihydroxydammar-24-ene-21-carboxylic acid 3-O-[¦Á-L-rhamnopyranosyl(1¡ú2)] [¦Â-D-glucopyranosyl(1¡ú3)]¦Â-D-glucopyranoside C48H80O18 ÏàËÆ¶È:68.6% Planta Medica 2012 78 597-605 New Dammarane-type Glycosides from the Roots of Gynostemma pentaphyllum Lei Ma,Wen-Juan Xiang, Pham Van Khang, Yang Liang, Yaping Xiao, Li-Hong Hu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 3¦Â,20S-dihydroxydammar-24-ene-21-carboxylic acid 3-O-{[¦Á-L-rhamnopyranosyl(1¡ú2)] [¦Â-D-glucopyranosyl(1¡ú3)]¦Â-D-glucopyranosyl}-21-O-¦Â-D-glucopyranoside C54H90O23 ÏàËÆ¶È:68.5% Planta Medica 2012 78 597-605 New Dammarane-type Glycosides from the Roots of Gynostemma pentaphyllum Lei Ma,Wen-Juan Xiang, Pham Van Khang, Yang Liang, Yaping Xiao, Li-Hong Hu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . ginsenoside Rs2 ÏàËÆ¶È:67.2% China Journal of Chinese Materia Medica 2013 38 2807-2817 Chemical constituents from roots and rhizomes of Panax ginseng cultivated in Jilin province WANG Hong-ping, YANG Xin-bao, YANG Xiu-wei*, LIU Jian-xun, WANG Ying-ping, ZHANG Lian-xue Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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