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1 .     stauntoside A
C48H72O19     ÏàËÆ¶È:79.1%
Phytochemistry          1999          52          1351-1355
Two C21-steroidal glycosides isolated from Cynanchum stauntoi
Nanqun Zhu, Mingfu Wang, Hiroe Kikuzaki, Nobuji Nakatani, Chi-Tang Ho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Argeloside I
C48H76O17     ÏàËÆ¶È:77.0%
Tetrahedron          2005          61          7470-7480
New antiproliferative 14, 15-secopregnane glycosides from Solenostemma argel
Alberto Plaza, Angela Perrone, Ciro Balestrieri, Maria Luisa Balestrieri, Giuseppe Bifulco, Virginia Carbone, Arafa Hamed, Cosimo Pizza, Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Argeloside C
C49H78O17     ÏàËÆ¶È:75.5%
Tetrahedron          2005          61          7470-7480
New antiproliferative 14, 15-secopregnane glycosides from Solenostemma argel
Alberto Plaza, Angela Perrone, Ciro Balestrieri, Maria Luisa Balestrieri, Giuseppe Bifulco, Virginia Carbone, Arafa Hamed, Cosimo Pizza, Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     3-O-[bis-¦Á-L-rhamnopyranosyl-(1¡ú2 and 1¡ú4)-¦Â-D-glucopyranosyl]-25R-furost-5-ene-3b,22¦Á,26-triol
C45H74O17     ÏàËÆ¶È:72.3%
Planta Medica          2004          70          637-641
Microbial Metabolism of Pseudoprotodioscin
Mei Dong,Xizhi Feng,Ben-Xiang Wang, Takashi Ikejima,Li-Jun Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (25R)-spirost-5-en-2¦Á,3¦Â-diol 3-O-¦Á‑L-rhamnopyranosyl-(1¡ú2)-[¦Á‑L-rhamnopyranosyl-(1¡ú4)]-¦Â‑D-glucopyranoside
C45H72O17     ÏàËÆ¶È:72.3%
Planta Medica          2012          78          276¨C285
Spirostanol Saponins Derivated from the Seeds of Trigonella foenum-graecum by ¦Â-Glucosidase Hydrolysis and Their Inhibitory Effects on Rat Platelet Aggregation
Xu Pang, Yue Cong, He-Shui Yu, Li-Ping Kang, Bing Feng, Bing-Xing Han, Yang Zhao, Cheng-Qi Xiong,Da-Wei Tan,Wei Song, Bin Liu, Yu-Wen Cong, Bai-Ping Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (22R,25R)-16¦Â-H-22¦Á-N-spirosol-3¦Â-ol-5-ene 3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-[¦Á-L-rhamnopyranosyl-(1¡ú4)]-¦Â-D-glucopyranoside
C45H73NO15     ÏàËÆ¶È:72.3%
Phytochemistry          2011          72          668-673
Steroidal alkaloid saponins and steroidal saponins from Solanum surattense
Yuanyuan Lu, Jianguang Luo, Lingyi Kong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     sublanceoside J2
C48H74O18     ÏàËÆ¶È:70.8%
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   Ì¼Æ×Ä£Äâͼ
8 .     solaverine I
    ÏàËÆ¶È:70.2%
Chemical & Pharmaceutical Bulletin          1990          38          827-829
STRUCTURES OF THREE NEW STEROIDAL ALKALOID GLYCOSIDES, SOLAVERINES I, II AND III FROM SOLANUM TOXICARIUM AND S. VERBASCIFOLIUM
Tomoyuki YAMASHITA,Nobuyo FUJIMURA,Shoji YAHARA,Toshihiro NOHARA,Syuji KAWANOBU and Kunimitsu FUJIEDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (25R) spirost-5-ene-3¦Â,14¦Á-diol-3-¦Â-O-¦Â-L-rhamnopyranosyl(l¡ú 2)-[¦Â-D-xylopyranosyl(l ¡ú 4)]-¦Â-D-glucopyranoside
C44H70O17     ÏàËÆ¶È:70.2%
Chinese Chemical Letters          2008          19          825-828
Two new steroidal glucosides from Ophiopogon japonicus (L.f.) Ker-Gawl
Ya Jiuan Xu, Tun Hai Xu, Ling Zhu Hao, Hong Feng Zhao, Sheng Xu Xie, Yun Shan Si, Dong Han, Dong Ming Xu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound 19
C49H78O18     ÏàËÆ¶È:70.2%
Phytochemistry          2000          53          485-498
Steroidal glycosides from the aerial part of Asclepias incarnata
Tsutomu Warashina, Tadataka Noro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     leptinine II
C45H73NO16     ÏàËÆ¶È:70.2%
Phytochemistry          1998          49          893-897
Steroidal alkaloid glycosides from Solanum orbignianum
Rosemary Matias Coelho, Maria Conceição De Souz¦Á, Maria Helena Sarragiotto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     Solamargine
    ÏàËÆ¶È:70.2%
Phytochemistry          1995          39          1475-1477
Steroid alkaloid glycosides from Solanum robustum
Helmut Ripperger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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