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niebiao2008: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2014-01-10 17:19:17
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²éѯ½á¹û£º¹²²éµ½3803¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¡÷20(22)-sarsaparilloside ÏàËÆ¶È:77.1% Steroids 2012 77 602-608 NMR assignment of the absolute configuration of C-25 in furostanol steroidal saponins Victoria L. Challinor, Sonia Piacente, James J. De Voss Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . tuberoside C C51H84O23 ÏàËÆ¶È:74.0% Phytochemistry 1999 52 1611-1615 Furostanol saponins from Allium tuberosum Shengmin Sang, Aina Lao, Hongcheng Wang, Zhongliang Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . pseudoprotodioscin C51H82O21 ÏàËÆ¶È:74.0% Research Journal of Phytochemistry 2008 2 100-105 Protodioscin and Pseudoprotodioscin From Solanum intrusum Essam Abdel-Sattar, Marwan M. Shabana and Sahar El-Mekkawy Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (25R)-26-[(¦Â-D-glucopyranosyl)oxy]-5¦Â-furost-20(22)-en-3¦Â-yl O-¦Â-D-glucopyranosyl-(1¡ú4)-O-[¦Á-L-rhamnopyranosyl-(1¡ú2)]-¦Â-D-glucopyranoside C51H84O22 ÏàËÆ¶È:74.0% Steroids 2013 78 670-682 Steroidal glycosides from the bulbs of Fritillaria meleagris and their cytotoxic activities Yukiko Matsuo, Daisuke Shinoda, Aina Nakamaru, Yoshihiro Mimaki Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . solanigroside F C56H92O28 ÏàËÆ¶È:73.2% Journal of Natural Products 2006 69 1158-1163 Steroidal Saponins from Solanum nigrum Xinlan Zhou, Xiangjiu He, Guanghui Wang, Hao Gao, Guangxiong Zhou, Wencai Ye, and Xinsheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . eryngioside B C54H90O24 ÏàËÆ¶È:72.2% Phytochemistry 2008 69 2070-2080 Phenolic compounds and rare polyhydroxylated triterpenoid saponins from Eryngium yuccifolium Zhizhen Zhang, Shiyou Li,Stacy Ownby, Ping Wang, Wei Yuan, Wanli Zhang, R. Scott Beasley Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . timosapoin B IV C51H84O23 ÏàËÆ¶È:72.2% Chinese Chemical Letters 2007 18 171-174 Two new saponins from Anemarrhena asphodeloides Bge Ying Peng, Yu Jing Zhang , Zhi Qiang Ma, Wei San Pan, Yu Qing Sun,Shao Jiang Song Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 15-methoxy-pseudoprotodioscin (25R) 26-O-¦Â-D-glucopyranosyl-5,20-diene-15-methoxy-3¦Â,26-dihydroxyfurost 3-O-[¦Á-L-rhamnopyranosyl(l ¡ú 2)][¦Á-L-rhamnopyranosyl(1 ¡ú 4)]-¦Â-D-glucopyranoside C52H84O22 ÏàËÆ¶È:72.2% Magnetic Resonance in Chemistry 2009 47 741-745 Structural determination of two new steroidal saponins from Smilax china (pages 741¨C745) Hui-Lian Huang, Rong-Hua Liu and Feng Shao Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 26-O-¦Â-D-glucopyranosyl-(25R)-furost-5(6)-en-3¦Â,22¦Â,26-triol-3-O-¦Á-L-rhamnopyranosyl-(1''¡ú 2')-O-[¦Â-D-glucopyranosyl-(1'''¡ú 6')-O]-¦Â-D-glucopyranoside ÏàËÆ¶È:72.2% Food Chemistry 2005 93 205-214 Furostanol saponins in Allium caepa L. Var. tropeana seeds Irene Dini, Gian Carlo Tenore, Elena Trimarco, Antonio Dini Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 26-O-¦Â-D-glucopyranosyl-22-O-methyl-(25R)-furost-5(6)-en-3¦Â,22¦Î,26-triol-3-O-¦Á-L-rhamnopyranosyl-(1''¡ú2')-O-[¦Â-D-glucopyranosyl-(1'''¡ú 6')-O]-¦Â-D-glucopyranoside ÏàËÆ¶È:72.2% Food Chemistry 2005 93 205-214 Furostanol saponins in Allium caepa L. Var. tropeana seeds Irene Dini, Gian Carlo Tenore, Elena Trimarco, Antonio Dini Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . tuberoside S C51H84O22 ÏàËÆ¶È:72.2% Food Chemistry 2003 83 499-506 New steroid saponins from the seeds of Allium tuberosum L. Shengmin Sang, Shilong Mao, Aina Lao, Zhongliang Chen, Chi-Tang Ho Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3-O-{¦Á-L-rhamnopyranosyl-(1¡ú2)-[¦Â-D-glucopyranosyl-(1¡ú4)]-¦Â-D-glucopyranoside}-26-O-¦Â-D-glucopyranoside C51H82O23 ÏàËÆ¶È:72.2% Magnetic Resonance in Chemistry 2012 50 755-758 Revised structures of avenacosides A and B and a new sulfated saponin from Avena sativa L. Łukasz Pecio, Dariusz Jędrejek, Milena Masullo, Sonia Piacente, Wiesław Oleszek and Anna Stochmal Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Lycianthoside C C51H84O23 ÏàËÆ¶È:72.2% Journal of Agricultural and Food Chemistry 2005 53 289-294 Three New Furostanol Saponins from the Leaves of Lycianthes synanthera (¡°Chomte¡±), an Edible Mesoamerican Plant Anna Lisa Piccinelli, Julieta Salazar De Ariza, Rub¨¨n Vel¨¤squez Miranda, Silvia Quesada Mora, Rita Aquino, and Luca Rastrelli Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . lycianthoside C C51H84O23 ÏàËÆ¶È:72.2% Journal of Agricultural and Food Chemistry 2005 53 289-294 Three New Furostanol Saponins from the Leaves of Lycianthes synanthera (¡°Chomte¡±), an Edible Mesoamerican Plant Anna Lisa Piccinelli, Julieta Salazar De Ariza, Rub¨¨n Vel¨¤squez Miranda, Silvia Quesada Mora, Rita Aquino, and Luca Rastrelli Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . macrostemonoside E C57H91O28 ÏàËÆ¶È:71.9% Acta Pharmaceutica Sinica 1993 28 526-531 STUDIES ON TWO NEW FUROSTANOL GLYCOSIDES FROM ALLIUM MACROSTEMON BUNGE JP Peng; X Wang and XS Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . multifidoside C57H92O27 ÏàËÆ¶È:71.9% Zeitschrift f¨¹r Naturforschung C 2002 57 603-608 Nuatigenin-Type Steroidal Saponins from Veronica fuhsii and V multifida M. Ozipek, I. Saracoglu, Y. Ogihara, and \.I. Çali\cs Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 3-O-{¦Á-L-rhamnopyranosyl-(1¡ú2)-[¦Â-D-glucopyranosyl-(1¡ú3)-¦Â-D-glucopyranosyl-(1¡ú4)]-¦Â-D-glucopyranoside}-26-O-¦Â-D-glucopyranoside C57H92O28 ÏàËÆ¶È:71.9% Magnetic Resonance in Chemistry 2012 50 755-758 Revised structures of avenacosides A and B and a new sulfated saponin from Avena sativa L. Łukasz Pecio, Dariusz Jędrejek, Milena Masullo, Sonia Piacente, Wiesław Oleszek and Anna Stochmal Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . tigogeninn3-O-¦Á-L-rhamnopyranosyl-(1 ¡ú3)-¦Â-D-glucopyranosyl-(1 ¡ú-)-[¦Â-D-xylopyranosyl-(1 ¡ú3) ]-¦Â-D-glucopyranosyl-(1 ¡ú4)-¦Â-D-galactopyranoside ÏàËÆ¶È:71.4% Acta Botanica Yunnanica 2002 24(4) 539-542 A New Steroidal Saponin from Fermented Leaves of Agave americana J IN Jian-Ming,LIU Xi-Kui,YANG Chong-Ren Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . dongnoside C C36H92O26 ÏàËÆ¶È:71.4% Phytochemistry 1989 28 2787-2791 Steroidal saponins from a cultivated form of Agave sisalana Ding Yi,Chen Yan-Yong,Wang De-Zu,Yang Chong-Ren Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . calendasaponin C C54H86O25 ÏàËÆ¶È:70.3% Chemical & Pharmaceutical Bulletin 2001 49(7) 863-870 Medicinal Flowers. III.1) Marigold. (1): Hypoglycemic, Gastric Emptying Inhibitory, and Gastroprotective Principles and New Oleanane-Type Triterpene Oligoglycosides, Calendasaponins A, B, C, and D, from Egyptian Calendula officinalis Masayuki YOSHIKAWA, Toshiyuki MURAKAMI, Akinobu KISHI, Tadashi KAGEURA, and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . hirtifolioside B C50H82O23 ÏàËÆ¶È:70.3% Planta Medica 2005 71 1010-1018 Structure-Activity Relationships for Saponins from Allium hirtifolium and Allium elburzense and their Antispasmodic Activity Elisa Barile,Raffaele Capasso,Angelo A. Izzo,Virginia Lanzotti,S. Ebrahim Sajjadi,Behza |
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