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14.72,15.17,15.55,16.46,17.41,17.93,18.3,18.44,19.32,21.00,21.10,23.18,24.48,27.53,27.86,28.31,30.45,32.16,32.71,36.19,37.74,39.23,40.36,45.51,46.60,52.88,53.04,55.4,58.01,63.49,64.02,67.85,68.87,69.31,69.55,71.39,72.65,76.16,76.38,82.17,85.83,86.64,92.86,93.72,96.63,99.91,100.63,159.95,172.07,175.53,201.27
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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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×Ä£Äâͼ
2Â¥2014-09-12 20:15:16
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