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1 .     scillascilloside D-1
    ÏàËÆ¶È:71.1%
Chemical & Pharmaceutical Bulletin          1994          42          327-332
Lanosterol Oligosaccharides from the Plants of the Subfamily Scilloideae and Their Antitumor-Promoter Activity
Yoshihiro MIMAKI,Hoyoku NISHINO,Kazutomo ORI,Minpei KURODA,Tomoko MATSUI and Yutaka SASHIDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     3¦Â-O-[¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl]-22S-hydroxycycloart-24E-en-26-oic acid
C48H78O19     ÏàËÆ¶È:69.3%
Phytochemistry          1994          37          515-519
Cycloartane glucosides from juncus effusus
Maria Michela Corsaro, Marina della Greca, Antonio Fiorentino, Pietro Monaco, Lucio Previtera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     peruvianoside A
C49H78O20     ÏàËÆ¶È:69.3%
Bulletin of the Chemical Society of Japan          1993          66          1182-1186
Peruvianosides A and B, Novel Triterpene Glycosides from the Bulbs of Scilla peruviana
Yoshihiro Mimaki, Kazutomo Ori, Yutaka Sashida, Tamotsu Nikaido, Lian-Gang Song, Taichi Ohmoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     23-epi-15-deoxoeucosterol 3-O-{O-¦Á-L-rhamnopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranosyl-(1¡ú2)-O-¦Á-L-arabinopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside }
C52H84O22     ÏàËÆ¶È:69.2%
Chemical & Pharmaceutical Bulletin          1994          42          327-332
Lanosterol Oligosaccharides from the Plants of the Subfamily Scilloideae and Their Antitumor-Promoter Activity
Yoshihiro MIMAKI,Hoyoku NISHINO,Kazutomo ORI,Minpei KURODA,Tomoko MATSUI and Yutaka SASHIDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     3¦Â,20S,21-trihydroxydamma¦Á-24-ene 3-O-{[¦Á-L-rhamnopyranosyl(1¡ú2)][¦Â-D-glucopyranosyl(1¡ú3)]-¦Â-D-glucopyranosyl}-21-O-¦Â-D-glucopyranoside
C54H92O22     ÏàËÆ¶È:68.5%
Journal of Natural Products          2004          67          942-952
Dammarane-Type Glycosides from Gynostemma pentaphyllum
Feng Yin, Lihong Hu, Fengchang Lou, and Ruixiang Pan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     3¦Â,-20S,21-trihydroxydammar-24-ene 3-O-{[¦Á-L-rhamnopyranosyl-(1¡ú2)][¦Â-D-glucopyranosyl (1¡ú3)]-¦Á-L-arabinopyranosyl}-21-O-¦Â-D-glucopyranoside
C53H90O21     ÏàËÆ¶È:67.9%
Journal of Natural Products          2006          69          1394-1398
Triterpene Saponins from Gynostemma cardiospermum
Feng Yin, Yinan Zhang, Zhengyi Yang, Qiuqun Cheng, and Lihong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     3¦Â,20S,21-trihydroxydamma¦Á-24-ene 3-O-{[¦Á-L-rhamnopyranosyl(1¡ú2)][¦Â-D-xylopyranosyl(1¡ú3)]-¦Â-D-glucopyranosyl}-21-O-¦Â-D-glucopyranoside
C53H90O21     ÏàËÆ¶È:67.9%
Journal of Natural Products          2004          67          942-952
Dammarane-Type Glycosides from Gynostemma pentaphyllum
Feng Yin, Lihong Hu, Fengchang Lou, and Ruixiang Pan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     scillascilloside D-1
    ÏàËÆ¶È:67.9%
Chemical & Pharmaceutical Bulletin          1994          42          327-332
Lanosterol Oligosaccharides from the Plants of the Subfamily Scilloideae and Their Antitumor-Promoter Activity
Yoshihiro MIMAKI,Hoyoku NISHINO,Kazutomo ORI,Minpei KURODA,Tomoko MATSUI and Yutaka SASHIDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     (23S,25R)-3¦Â,30,31-trihydroxy-17¦Á,23-epoxy-5¦Á-lanost-5-en-23,26-olactone 3-O-{O-¦Á-L-rhamopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranosyl-(1¡ú2)-O-¦Á-L-arabinopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside }
C53H84O24     ÏàËÆ¶È:67.9%
Chemical & Pharmaceutical Bulletin          1994          42          327-332
Lanosterol Oligosaccharides from the Plants of the Subfamily Scilloideae and Their Antitumor-Promoter Activity
Yoshihiro MIMAKI,Hoyoku NISHINO,Kazutomo ORI,Minpei KURODA,Tomoko MATSUI and Yutaka SASHIDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (20S)-3¦Â,20,21-Trihydroxydammara-23,25-diene 3-O-[¦Á-L-Rhamnopyranosyl-(1¡ú2)][¦Â-D-xylopyranosyl-(1¡ú3)]-¦Â-D-glucopyranosyl-21-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:67.9%
Helvetica Chimica Acta          2010          93          1785-1794
Three New Triterpene Saponins from Gynostemma pentaphyllum
Lin Shi, Jia-Qing Cao, Wei Li and Yu-Qing Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     Khekadaengoside M
C48H82O18     ÏàËÆ¶È:67.3%
Phytochemistry          2002          59          215-228
Cucurbitane, hexanorcucurbitane and octanorcucurbitane glycosides from fruits of Trichosanthes tricuspidata
Tripetch Kanchanapoom, Ryoji Kasai, Kazuo Yamasaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     (25S)-5¦Á-spirostan-3¦Â-ol-3-O-¦Â-D-galactopyranosyl(1¡ú2)-¦Â-D-glucopyranosyl(1¡ú4)-¦Â-D-galactopyranoside
    ÏàËÆ¶È:67.3%
Chemical Research in Chinese Universities          2010          26          915-921
Separation and Bio-activities of Spirostanol Saponin from Tribulus terrestris
ZHANG Shuang, YANG Rui-jie, LI Hong, YIN Zong-yuan, ZHOU Hong-yu,LI Xu-wen, JIN Yong-ri and YANG Shi-jie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     peruvianoside B
C49H78O21     ÏàËÆ¶È:67.3%
Bulletin of the Chemical Society of Japan          1993          66          1182-1186
Peruvianosides A and B, Novel Triterpene Glycosides from the Bulbs of Scilla peruviana
Yoshihiro Mimaki, Kazutomo Ori, Yutaka Sashida, Tamotsu Nikaido, Lian-Gang Song, Taichi Ohmoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     3¦Â,-19,20S,21-tetrahydroxydamma¦Á-24-ene 3-O-{[¦Á-L-rhamnopyranosyl(1¡ú2)][¦Â-D-xylopyranosyl(1¡ú3)]-¦Á-L-arabinopyranosyl}-21-O-¦Â-D-glucopyranoside
C52H88O21     ÏàËÆ¶È:67.3%
Journal of Natural Products          2004          67          942-952
Dammarane-Type Glycosides from Gynostemma pentaphyllum
Feng Yin, Lihong Hu, Fengchang Lou, and Ruixiang Pan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     muscaroside C
    ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1994          42          327-332
Lanosterol Oligosaccharides from the Plants of the Subfamily Scilloideae and Their Antitumor-Promoter Activity
Yoshihiro MIMAKI,Hoyoku NISHINO,Kazutomo ORI,Minpei KURODA,Tomoko MATSUI and Yutaka SASHIDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     scillasaponin D
C53H84O24     ÏàËÆ¶È:66.0%
Phytochemistry          1993          34          791-797
Lanosterol and 27-norlanosterol oligosaccharides from the bulbs of Chionodoxa gigantea
Yoshihiro Mimaki, Satoshi Kubo, Youji Kinoshita, Yutaka Sashida, Lian-Gang Song, Tamotsu Nikaido, Taichi Ohmoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     (23S,25R)-3¦Â,30,31-trihydroxy-17¦Á,23-epoxy-5¦Á-lanost-5-en-23,26-olactone 3-O-{O-¦Â-apio-D-furanosyl-(1¡ú2)-O-¦Â-D-glucopyranosyl-(1¡ú2)-O-¦Á-L-arabinopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside }
C52H86O24     ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          1994          42          327-332
Lanosterol Oligosaccharides from the Plants of the Subfamily Scilloideae and Their Antitumor-Promoter Activity
Yoshihiro MIMAKI,Hoyoku NISHINO,Kazutomo ORI,Minpei KURODA,Tomoko MATSUI and Yutaka SASHIDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     sapinmusaponin R
C49H80O17     ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          2007          55(9)          1412-1415
Anti-platelet Aggregation Triterpene Saponins from the Galls of Sapindus mukorossi
Hui-Chi HUANG,Wei-Jern TSAI,Chia-Ching LIAW,Shih-Hsiung WU,Yang-Chang WU,and Yao-Haur KUO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     Acanjaposide F
C48H76O20     ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          2005          53(9)          1147-1151
New Oleanene Glycosides from the Leaves of Acanthopanax japonicus
Sang-Yong PARK,Chang-Soo YOOK,and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     Rotundifolioside E
C47H76O17     ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          2003          51(4)          365-37
Antiproliferative Constituents from Umbelliferae Plants VI.1,2) New Ursane-Type Saikosaponin Analogs from the Fruits of Bupleurum rotundifolium
Toshihiro FUJIOKA,Keisuke YOSHIDA, Hiroko FUJII, Tsuneatsu NAGAO, Hikaru OKABE, and Kunihide MIHASHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     abutiloside H
    ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          2002          50(2)          284-286
Four New 26-Aminocholestane-Type Glycosides from Solanum abutiloides
Hitoshi YOSHIMITSU,Makiko NISHIDA, Mitsuko YOSHIDA,and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     abutiloside J
C48H81NO17     ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          2002          50(2)          284-286
Four New 26-Aminocholestane-Type Glycosides from Solanum abutiloides
Hitoshi YOSHIMITSU,Makiko NISHIDA, Mitsuko YOSHIDA,and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     lucilianoside A
C48H76O23     ÏàËÆ¶È:65.3%
Phytochemistry          2003                   1351-1359
Lanosterol and tetranorlanosterol glycosides from the bulbs of Muscari paradoxum
Kazutomo Ori, Minpei Koroda, Yoshihiro Mimaki,Hiroshi Sakagami, Yutaka Sashida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     11¦Á,12¦Á-epoxy-3¦Â-[(O-¦Â-D-galactopyrano-syl-(1¡ú3)-O-[¦Â-D-glucopyranosyl-(1¡ú2)]-¦Â-D-glucuronopyranosyl)-oxy]olean-28,13-olide
C48H74O20     ÏàËÆ¶È:65.3%
Journal of Natural Products          2006          69          1606-1610
Oleanane and Taraxerane Glycosides from the Roots of Gomphrena macrocephala
Minpei Kuroda, Taku Aoshima, Mitsue Haraguchi, Maria Cludia Marx Young, Hiroshi Sakagami, and Yoshihiro Mimaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     eryloside V
C48H80C17     ÏàËÆ¶È:65.3%
Journal of Natural Products          2007          70          1871-1877
Isolation and Structures of Erylosides from the Carribean Sponge Erylus goffrilleri
Shamil Sh. Afiyatullov,Anatoly I. Kalinovsky, Alexandr S. Antonov, Ludmila P. Ponomarenko, Pavel S. Dmitrenok,Dmitry L. Aminin, Vladimir B. Krasokhin, Valentina M. Nosova, and Alexandr V. Kisin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     6-O-¦Á-L-rhamnopyranosyl-16,24-di-O-¦Â-D-glucopyranosyl-3¦Â,6¦Á,16¦Â,24(S),25-pentahydroxy-cycloartane
C48H82O19     ÏàËÆ¶È:65.3%
Phytochemistry          2009          70          628-634
Cycloartane-type glycosides from Astragalus amblolepis
Emre Polat, Ozgen Caliskan-Alankus, Angela Perrone, Sonia Piacente, Erdal Bedir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     abutiloside A
    ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          1996          44          1119-1121
Cholestane Glycosides from Solanum abutiloides
Rui-Hua TIAN,Emi OHMURA,Hitoshi YOSHIMITSU,Toshihiro NOHARA and Masaharu MATSUI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     anagallosaponin III
C48H78O18     ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          1994          42          1750-1755
Structures of Anagallosaponins I-V and Their Companion Substances from Anagallis arvensis L.
Noboru SHOJI,Akemi UMEYAMA,Kazuko YOSHIKAWA and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     kaikasaponin III methyl ester
    ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          1992          40          2995-2999
Triterpene Glycosides from the Bark of Robinia pseudo-acacia L. I
Baoliang CUI,Junei KINJO and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     compound 2
    ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          1986          34          1158-1167
Chemical Evaluation of Bupleurum Species Collected in Yunnan, China
JING-KAI DING,HIROKO FUJINO(nee KIMATA),RYOJI KASAI,NAOKO FUJIMOTO,OSAMU TANAKA,JUN ZHOU,HIROMICHI MATSUURA and TOHRU FUWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     Glycoside L-I1
    ÏàËÆ¶È:65.3%
Chemistry of Natural Compounds          2000          36          506-509
TRITERPENOID GLYCOSIDES OF Scheffleropsis angkae.III. STRUCTURE OF GLYCOSIDE L-I1
V. V. Kachala, A. S. Stolyarenko, V. I. Grishkovets,A. S. Shashkov, and V. Ya. Chirva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     abutiloside A
C49H83NOI7     ÏàËÆ¶È:65.3%
Phytochemistry          1997          44          723-726
Abutiloside A, A 26-acylamino-3¦Â, 16¦Á-dihydroxy-5¦Á-cholesta-22-one glycoside from Solanum abutiloides
Rui-Hua Tian, Emi Ohmura, Masaharu Matsui, Toshihiro Noharas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     anagallosaponin III
    ÏàËÆ¶È:65.3%
Phytochemistry          1994          37          1397-1402
Triterpenoid glycosides from Anagallis arvensis
Noboru Shoji, Akemi Umeyama, Kazuko Yoshikawa, Shigenobu Arihara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     3¦Â,20S,21-trihydroxydammar-24-ene 3-O-[¦Á-L-rhamnopyranosyl(1¡ú2)][¦Â-D-glucopyranosyl(1¡ú3)]¦Â-D-glucopyranoside
C48H82O17     ÏàËÆ¶È:65.3%
Planta Medica          2012          78          597-605
New Dammarane-type Glycosides from the Roots of Gynostemma pentaphyllum
Lei Ma,Wen-Juan Xiang, Pham Van Khang, Yang Liang, Yaping Xiao, Li-Hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     carnosiflosideVI
C48H80O18     ÏàËÆ¶È:65.3%
Phytochemistry          1987          26          1371-1376
Sweet and bitter cucurbitane glycosides from hemsleya carnosiflora
Ryoji Kasai,Kazuhiro Matsumoto,Rui-Lin Nie,Toshinobu Morita,Akimi Awazu,Jun Zhou,Osamu Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     Compound 7
C48H80O15     ÏàËÆ¶È:65.3%
Bioorganic & Medicinal Chemistry Letters          2009          19          2310-2314
Synthesis, cytotoxicity, and haemolytic activity of chacotrioside lupane-type neosaponins and their germanicane-type rearrangement products
Charles Gauthier, Jean Legault, Marianne Piochon, Serge Lavoie, Samuel Tremblay, Andr¨¦ Pichette
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     saikosaponin c
    ÏàËÆ¶È:65.3%
Journal of China Pharmaceutical University          2003          34          305-308
Study on the Constituents of the Roots of Bupleurum marginatum
LIANG Zhi-Tao; QIN Min-Jian; TANG Li; WANG Zheng-Tao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     3-O-[¦Á-L-Rhamnopyranosyl (1¡ú2)-¦Â-D-galactopyranosyl (1¡ú2)-¦Â-D-glucuronopyranosyl]-complogenin
C48H76O19     ÏàËÆ¶È:65.3%
Zeitschrift f¨¹r Naturforschung C          2005          60          813-820
Bioactive Saponins from Astragalus suberi L. Growing in Yemen
F. Abbas and R. Zayed
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     anagallosaponin V
C54H88O23     ÏàËÆ¶È:64.8%
Chemical & Pharmaceutical Bulletin          1994          42          1750-1755
Structures of Anagallosaponins I-V and Their Companion Substances from Anagallis arvensis L.
Noboru SHOJI,Akemi UMEYAMA,Kazuko YOSHIKAWA and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     Thalictoside C
    ÏàËÆ¶È:64.8%
Chemistry of Natural Compounds          2005          41          117-140
STRUCTURAL STUDIES AND BIOLOGICAL ACTIVITY OF PLANT TRITERPENOIDS FROM THE Thalictrum GENUS
V. I. Lutskii, A. S. Gromova,E. A. Khamidullina, and N. L. Owen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

41 .     Glycoside A
C54H88O22     ÏàËÆ¶È:64.8%
Chemical Research in Chinese Universities          1994          10          185-192
Studies on the Glycosides in the Leaves of Oplopanax elatus NAKAI(I)
WANG Guang-shu,ZHAO Chun-fang and XU Jing-da
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

42 .     Pavioside A
    ÏàËÆ¶È:64.8%
Bioorganic & Medicinal Chemistry          2012          20          3280-3286
Paviosides A¨CH, eight new oleane type saponins from Aesculus pavia with cytotoxic activity Original Research Article
Virginia Lanzotti, Pasquale Termolino, Marcello Dolci, Paolo Curir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

43 .     Pavioside B
    ÏàËÆ¶È:64.8%
Bioorganic & Medicinal Chemistry          2012          20          3280-3286
Paviosides A¨CH, eight new oleane type saponins from Aesculus pavia with cytotoxic activity Original Research Article
Virginia Lanzotti, Pasquale Termolino, Marcello Dolci, Paolo Curir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

44 .     glycoside 3
C53H90O21     ÏàËÆ¶È:64.1%
Chemical & Pharmaceutical Bulletin          2004          52(12)          1440-1444
Novel Dammarane-Type Glycosides from Gynostemma pentaphyllum
Feng YIN, Lihong HU,and Ruixiang PAN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

45 .     3¦Â,19,20S,21-tetrahydroxydamma¦Á-24-ene 3-O-{[¦Á-Lrhamnopyranosyl(1¡ú2)][¦Â-D-xylopyranosyl(1¡ú3)]-¦Â-D-glucopyranosyl}-21-O-¦Â-D-glucopyranoside
C53H90O22     ÏàËÆ¶È:64.1%
Journal of Natural Products          2004          67          942-952
Dammarane-Type Glycosides from Gynostemma pentaphyllum
Feng Yin, Lihong Hu, Fengchang Lou, and Ruixiang Pan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

46 .     3¦Â-O-{¦Â-D-xylopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranosyl-(1¡ú4)-[O-¦Â-D-glucopyranosyl-(1¡ú2)]-¦Á-L-arabinopyranosyl}-16¦Á-hydroxy-13¦Â,28-epoxy oleanane
    ÏàËÆ¶È:64.1%
Journal of Natural Products          1994          Vol 57          1354
Cytotoxic Saponins from New Zealand Myrsine Species
Stephen J. Bloor, Lu Qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

47 .     3¦Â-O-{¦Â-D-xylopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranosyl-(1¡ú4)-[O-¦Â-D-glucopyranosyl-(1¡ú2)]-¦Á-L-arabinopyranosyl}-16¦Á,28-dihydroxy-13¦Â,28-epoxy oleanane
    ÏàËÆ¶È:64.1%
Journal of Natural Products          1994          Vol 57          1354
Cytotoxic Saponins from New Zealand Myrsine Species
Stephen J. Bloor, Lu Qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

48 .     
    ÏàËÆ¶È:64%
Chemical & Pharmaceutical Bulletin          1992          40          2995-2999
Triterpene Glycosides from the Bark of Robinia pseudo-acacia L. I
Baoliang CUI,Junei KINJO and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

49 .     compound 1b
    ÏàËÆ¶È:64%
Chemistry of Natural Compounds          2005          41          436-441
TRITERPENE GLYCOSIDES FROM Cussonia paniculata.II. ACETYLATED GLYCOSIDES FROM LEAVES
V. I. Grishkovets, I. I. Dovgii, V. V. Kachala,and A. S. Shashkov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

50 .     phyteumoside A
C50H84O20     ÏàËÆ¶È:64%
Organic Letters          2011          Vol.13,No.6          1354-1357
Phyteumosides A and B: New Saponins with Unique Triterpenoid Aglycons from Phyteuma orbiculare L.
Christian Abbet, Markus Neuburger, Trixie Wagner, Melanie Quitschau,Matthias Hamburger, and Olivier Potterat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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