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aÇÒ¸èÇÒÐÐa: ½ð±Ò+10, ¡ïÓаïÖú 2014-09-12 20:39:27
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aÇÒ¸èÇÒÐÐa: ½ð±Ò+10, ¡ïÓаïÖú 2014-09-12 20:39:27
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²éѯ½á¹û£º¹²²éµ½1580¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 13 C52H84O17 ÏàËÆ¶È:66.6% Journal of Natural Products 2006 69(2) 240-246 Triterpenoid Saponins from Campsiandra guayanensis Alessandra Braca, Ayman F. Abdel-Razik, Jeannette Mendez, and Nunziatina De Tommasi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . glaucoside-I C48H74O20 ÏàËÆ¶È:62.7% Chemical & Pharmaceutical Bulletin 1983 31 2244-2253 Studies on the Constituents of Asclepiadaceae Plants. LV. The Structures of Three New Glycosides, Glaucoside-H, -I, and -J from the Chinese Drug "Pai-ch'ien, "Cynanchum glaucescens HAND-MAZZ TAKASHI NAKAGAWA,KOJI HAYASHI and HIROSHI MITSUHASHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . lanatosides C ÏàËÆ¶È:62.7% Pharmazie 1999 54 926-930 Phenylethanoid and cardioactive glycosides from Digitalis ferruginea I. Çalis - P. Akbay - A. Kuru¨¹z¨¹m - F.N. Yalçin - P. Sahin - G.F. Pauli Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . phillyriside A C48H76O17 ÏàËÆ¶È:62.7% Heterocycles 2012 85 1377-1392 New Triterpenoid Saponins from Stenocereus eruca Kazutaka Kakuta, Takeshi Koike, Kaoru Kinoshita, Satoru Ito, Kiyotaka Koyama, and Kunio Takahashi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . sublanceoside J2 C48H74O18 ÏàËÆ¶È:60.7% Chemical & Pharmaceutical Bulletin 2006 54(11) 1551-1560 Glycosides of 14,15-Seco and 13,14:14,15-Disecopregnanes from the Roots of Cynanchum sublanceolatum Tsutomu WARASHINA and Tadataka NORO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . stachyssaponin III C52H84O21 ÏàËÆ¶È:60.7% Chemical & Pharmaceutical Bulletin 1994 42 1291-1296 Stachyssaponins I-VIII, New Oleanane-Type Triterpene Saponins from Stachys riederi CHAMISSO Ryouko YAMAMOTO,Toshio MIYASE and Akira UENO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 4 C47H72O20 ÏàËÆ¶È:60.7% Steroids 2006 71 61-66 C-21 steroidal glycosides from the roots of Cynanchum chekiangense and their immunosuppressive activities Xiaoyu Li, Hongxiang Sun, Yiping Ye, Fengyang Chen, Yuanjiang Pan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . Codonolaside II ÏàËÆ¶È:60.7% Journal of Natural Medicines 2010 64 321-329 Murine metabolism and absorption of lancemaside A, an active compound in the roots of Codonopsis lanceolata Noriko Komoto, Makoto Ichikawa, Sanae Ohta, Daisuke Nakano and Takeshi Nishihama, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . lanatosides A ÏàËÆ¶È:60.7% Pharmazie 1999 54 926-930 Phenylethanoid and cardioactive glycosides from Digitalis ferruginea I. Çalis - P. Akbay - A. Kuru¨¹z¨¹m - F.N. Yalçin - P. Sahin - G.F. Pauli Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . codonolaside II C51H82O20 ÏàËÆ¶È:60.7% Pharmazie 2007 62 463-466 Triterpenoid saponins and anti-inflammatory activity of Codonopsis lanceolata Jian-Ping Li, Zhi-Min Liang and Zhong Yuan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . sublanceoside K2 C55H86O21 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2006 54(11) 1551-1560 Glycosides of 14,15-Seco and 13,14:14,15-Disecopregnanes from the Roots of Cynanchum sublanceolatum Tsutomu WARASHINA and Tadataka NORO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . asterlingulatoside C C52H84O21 ÏàËÆ¶È:59.6% Journal of Natural Products 1997 60 743-746 Asterlingulatosides C and D, Cytotoxic Triterpenoid Saponins from Aster lingulatus Yu Shao, Chi-Tang Ho, and Chee-Kok Chin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . Impatienoside G C52H82O22 ÏàËÆ¶È:59.6% Phytochemistry 2009 70 816-821 Triterpenoid saponins from Impatiens siculifer Wei Li, Xueyan Bi, Kun Wang, Dongxia Li, Tadaaki Satou, Kazuo Koike Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . foetidissimoside A ÏàËÆ¶È:59.6% Phytochemistry 1988 27 881-885 Foetidissimoside A,a new 3,28-bidesmosidic triterpenoid saponin,and cucurbitacins from Cucurbita foetidissima Marie-Aleth Dubois,Rudolf Bauer,M.Roberto Cagiotti,Hildebert Wagner Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . Foetidissimoside A ÏàËÆ¶È:59.6% Phytochemical Analysis 2008 19 403-410 Preparative separation of the saponin lancemaside a from Codonopsis lanceolata by centrifugal partition chromatography Osamu Shirota, Kumi Nagamatsu, Setsuko Sekita, Noriko Komoto, Masanori Kuroyanagi, Makoto Ichikawa, Sanae Ohta and Mitsuyasu Ushijima Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . ageratoside A4 C54H84O25 ÏàËÆ¶È:59.2% Phytochemistry 1999 51 309-318 Triterpenoid saponins from the ground part of Aster ageratoides var. ovatus Kazumi Sakai, Tsuneatsu Nagao, Hikaru Okabe Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . ¦Á-D-mannopyranosyl-(12)-¦Á-D-mannopyranosyl 3-O-[¦Á-D-mannopyranosyl-(12)-¦Á-D-mannopyranosyl] oleanolate C54H88O23 ÏàËÆ¶È:59.2% Bioorganic & Medicinal Chemistry 2009 17 5207-5218 Mannosylated saponins based on oleanolic and glycyrrhizic acids. Towards synthetic colloidal antigen delivery systems Alison M. Daines, Ben W. Greatrex, Colin M. Hayman, Sarah M. Hook, Warren T. McBurney, Thomas Rades, Phillip M. Rendle, Ian M. Sims Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . scheffarboside B C51H82O19 ÏàËÆ¶È:58.8% Helvetica Chimica Acta 2006 Vol. 89 468 Triterpenoid Saponins from Schefflera arboricola Fu-Jiang Guo, Pin Chen, Shu-Ying Peng, and Yuan-Chao Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . sublanceoside H2 C48H74O20 ÏàËÆ¶È:58.8% Chemical & Pharmaceutical Bulletin 2006 54(11) 1551-1560 Glycosides of 14,15-Seco and 13,14:14,15-Disecopregnanes from the Roots of Cynanchum sublanceolatum Tsutomu WARASHINA and Tadataka NORO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 12 C51H82O16 ÏàËÆ¶È:58.8% Journal of Natural Products 2006 69(2) 240-246 Triterpenoid Saponins from Campsiandra guayanensis Alessandra Braca, Ayman F. Abdel-Razik, Jeannette Mendez, and Nunziatina De Tommasi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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