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liyuan2008: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, лл 2013-10-09 21:04:27
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liyuan2008: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, лл 2013-10-09 21:04:27
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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£º¹²²éµ½218¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . batatsin III-3-O-glucoside C21H26O8 ÏàËÆ¶È:87.5% Phytochemistry 1997 44 1565-1567 Two bibenzyl glucosides from Pleione bulbocodioides Li Bai, Noriko Masukawa, Masae Yamaki, Shuzo Takagi Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Shancigusin E C23H28O9 ÏàËÆ¶È:79.1% Magnetic Resonance in Chemistry 2013 51 371-377 Shancigusins E-I, five new glucosides from the tubers of Pleione yunnanensis Hai-ling Dong, Han-qiao Liang, Chun-lan Wang, Shun-xing Guo and Jun-Shan Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3'-hydroxy-5-methoxybibenzyl-3-O-¦Â-D-glucopyranoside C21H26O8 ÏàËÆ¶È:75% Academic Journal of Second Military Medical University 2002 23 1029-1031 Studies on chemical constituents of Bletilla striata ¢ò HAN Guang-Xuan, WANG Li-Xin, ZHANG Wei-Dong, WANG Mai-Li, LIU Hong-Tao, XIAO Jian-Hua Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ¦Á,¦Â-dihydrorhaponticin C21H26O9 ÏàËÆ¶È:70.8% Phytochemistry 2006 67 2182-2188 Stilbenoids from Tragopogon orientalis Christian Zidorn, Sandra Grass, Ernst P. Ellmerer,Karl-Hans Ongania, Hermann Stuppner Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ¦Á,¦Á'-dihydro-3,3'-dihydroxy-5¦Â-D-O-glucopyranosyloxy-4'-methoxystilbene C21H26O9 ÏàËÆ¶È:70.8% Journal of Natural Products 2005 68 1099-1102 Dihydrostilbene Derivatives from Glycyrrhiza glabra Leaves Daniela M. Biondi, Concetta Rocco, and Giuseppe Ruberto Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3',5-dimethoxybibenzyl-3-O-¦Â-D-glucopyranoside C22H28O8 ÏàËÆ¶È:70.8% Phytochemistry 1997 44 1565-1567 Two bibenzyl glucosides from Pleione bulbocodioides Li Bai, Noriko Masukawa, Masae Yamaki, Shuzo Takagi Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3'-¦Â-D-Glucopyranosyloxy-4,5'-dihydroxy-3-methoxy-1,2-diphenylethnne C21H26O9 ÏàËÆ¶È:70.8% European Journal of Organic Chemistry 1992 1992 399-401 Syntheses of Some Biologically Active Compounds from Stilbenes Isolated from the Bark of Picea abies Antti Talvitie, Erkki Mannila and Erkki Kolehmainen Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3'-¦Â-D-Glucopyranosyloxy-3,4,5'-trihydroxy-1,2-diphenylethane ÏàËÆ¶È:70.8% European Journal of Organic Chemistry 1992 1992 399-401 Syntheses of Some Biologically Active Compounds from Stilbenes Isolated from the Bark of Picea abies Antti Talvitie, Erkki Mannila and Erkki Kolehmainen Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3'-¦Â-D-Glucopyranosyloxy-3,4,5'-trimethoxy-1,2-diph enylethane C23H30O9 ÏàËÆ¶È:70.8% European Journal of Organic Chemistry 1992 1992 399-401 Syntheses of Some Biologically Active Compounds from Stilbenes Isolated from the Bark of Picea abies Antti Talvitie, Erkki Mannila and Erkki Kolehmainen Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Shancigusin F C21H26O7 ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 2013 51 371-377 Shancigusins E-I, five new glucosides from the tubers of Pleione yunnanensis Hai-ling Dong, Han-qiao Liang, Chun-lan Wang, Shun-xing Guo and Jun-Shan Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3'-O-methyl-¦Á,¦Â-dihydrorhaponticin C22H28O9 ÏàËÆ¶È:62.5% Phytochemistry 2006 67 2182-2188 Stilbenoids from Tragopogon orientalis Christian Zidorn, Sandra Grass, Ernst P. Ellmerer,Karl-Hans Ongania, Hermann Stuppner Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . vittarin-C C22H25O10 ÏàËÆ¶È:62.5% Journal of Natural Products 2005 68 1180-1184 Constituents of Vittaria anguste-elongata and Their Biological Activities Pei-Lin Wu, Yu-Lin Hsu, Chen-Wei Zao, Amooru G. Damu, and Tian-Shung Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . vittarin-D C23H27O11 ÏàËÆ¶È:58.3% Journal of Natural Products 2005 68 1180-1184 Constituents of Vittaria anguste-elongata and Their Biological Activities Pei-Lin Wu, Yu-Lin Hsu, Chen-Wei Zao, Amooru G. Damu, and Tian-Shung Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 10-O-trans-p-coumaroyldesacetyl asperulosidic acid C25H28O13 ÏàËÆ¶È:58.3% Journal of Natural Products 2005 68 1646-1650 Iridoid Glycosides and Grayanane Diterpenoids from the Roots of Craibiodendron henryi Xiang-zhong Huang, Ying-hong Wang, Shi-shan Yu, Guang-miao Fu, You-cai Hu, Yue Liu, and Li-hua Fan Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . rhodanthenone A C19H20O10 ÏàËÆ¶È:58.3% CHEMISTRY & BIODIVERSITY 2011 8 1891-1900 Phenolic Compounds from the Whole Plants of Gentiana rhodantha (Gentianaceae) Min Xu, Ming Zhang, Dong Wang, Chong-Ren Yang and Ying-Jun Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ |

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