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15.7,16.5,17.5,18.4,18.8,23.8,24.5,27.1,28.0,28.7,30.7,32.1,33.1,33.4,35.8,36.0,37.3,39.0,39.3,40.0,41.2,42.0,47.2,47.2,49.1,55.8,61.2,69.2,70.2,70.7,72.5,72.7,73.8,73.9,74.2,75.2,76.4,77.9,78.0,78.2,78.6,95.7,102.6,104.8,122.6,144.4,176.0
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ÓñÃ×-Æ»¹û: ½ð±Ò+10 2015-06-19 10:59:36
tauroside J
    ÏàËÆ¶È:95.8%
Chemistry of Natural Compounds          1992          28          593-596
TRITERPENE GLYCOSIDES OF Hedera taurica X. STRUCTURES OF COMPOUNDS F 4, I, AND J FROM THE LEAVES OF CRIMEAN IVY
V. I. Grishkovets, N. V. Tolkacheva,A. S. Shashkov, and V. Ya. Chirva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     cussonside B
C48H78O17     ÏàËÆ¶È:91.6%
China Journal of Chinese Materia Medica          2001          26          612-614
Studies on the Chemical Constituents from Anemone anhuiensis Y. K. Yang n. Wang et W. C. Ye
ZHANG Qingwen, YE Wencai, CHE Chuntao, ZHAPO Shouxun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     Oleanolic acid 28-O-[¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl-(1¡ú6)] ¦Â-D-glucopyranoside
C48H78O17     ÏàËÆ¶È:91.6%
Natural Product Communications          2006          1          27-32
Clarification of the Saponin Composition ofRanunculus ficaria Tubers
Andrew Marston, Martine Cabo, Christian Lubrano, Jean-Renaud Robin,Claude Fromageot and Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     Yemuoside YM20
C48H78O18     ÏàËÆ¶È:89.5%
Helvetica Chimica Acta          2008          Vol. 91          451
Unusual Nortriterpenoid Saponins from Stauntonia chinensis
Hao Gao, ZhaoWang, Zhi-Hong Yao, NingWu, Hua-Jin Dong, Jin Li, Nai-LiWang, Wen-Cai Ye, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     tauroside I
    ÏàËÆ¶È:89.5%
Chemistry of Natural Compounds          1992          28          593-596
TRITERPENE GLYCOSIDES OF Hedera taurica X. STRUCTURES OF COMPOUNDS F 4, I, AND J FROM THE LEAVES OF CRIMEAN IVY
V. I. Grishkovets, N. V. Tolkacheva,A. S. Shashkov, and V. Ya. Chirva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     Durantanin IV
C48H78O20S     ÏàËÆ¶È:89.5%
Molecules          2009          14          1952-1965
New Triterpene Saponins from Duranta repens Linn. and Their Cytotoxic Activity
Wafaa S. Ahmed, Mona A. Mohamed, Rabab A. El-Dib and Manal M. Hamed
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     oleanolic acid 28-O-¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glccopyranosyl(1¡ú6)-¦Â-D-glccopyranosyl
    ÏàËÆ¶È:89.5%
China Journal of Chinese Materia Medica          2008          33          1696-1699
Studies on chemical constituents from rhizome of Anemone flaccida
ZHANG Lantian, TAKAISHI Yoshihisa, ZHANG Yanwen, DUAN Hongquan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     ciwujianoside C3
    ÏàËÆ¶È:89.5%
West China Journal of Pharmaceutical Sciences          1990          5          132-135
Studies on saponins isolated from Schettlera Delavayi Harms ex diels
Jian qenpen, Xian Zhuoyin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     Yemuoside YM17
C47H76O19     ÏàËÆ¶È:89.3%
Helvetica Chimica Acta          2008          Vol. 91          451
Unusual Nortriterpenoid Saponins from Stauntonia chinensis
Hao Gao, ZhaoWang, Zhi-Hong Yao, NingWu, Hua-Jin Dong, Jin Li, Nai-LiWang, Wen-Cai Ye, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     Gordonoside K
C47H74O19     ÏàËÆ¶È:89.3%
Journal of Natural Products          2011          74          1066-1072
Potential Anti-inflammatory Constituents of the Stems of Gordonia chrysandra
Hui-Zheng Fu, Chuang-Jun Li, Jing-Zhi Yang, Zhu-Fang Shen, and Dong-Ming Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     Acanjaposide H
C48H76O19     ÏàËÆ¶È:87.5%
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
--------------------------------------------------------------------------------

12 .     nipponoside D
    ÏàËÆ¶È:87.5%
Phytochemistry          2002          59          379-384
nor-Oleanene type triterpene glycosides from the leaves of Acanthopanax japonicus
Sang-Yong Park, Seung-Yeup Chang, O-Jin Oh,Chang-Soo Yook, Toshihiro Nohara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     kalopanax saponin G
    ÏàËÆ¶È:87.5%
Journal of Natural Products          1999          62          445-448
Triterpenoid Saponins of Acanthopanax nipponicus Leaves
Masazumi Miyakoshi, Katsuya Shirasuna, Yasuaki Hirai, Kazushi Shingu, Susumu Isoda, Junzo Shoji, Yoshiteru Ida, and Torao Shimizu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

14 .     nipponoside D
C48H78O19     ÏàËÆ¶È:87.5%
Journal of Natural Products          1999          62          445-448
Triterpenoid Saponins of Acanthopanax nipponicus Leaves
Masazumi Miyakoshi, Katsuya Shirasuna, Yasuaki Hirai, Kazushi Shingu, Susumu Isoda, Junzo Shoji, Yoshiteru Ida, and Torao Shimizu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     kalopanaxsaponin G
C48H78O18     ÏàËÆ¶È:87.5%
Chemical & Pharmaceutical Bulletin          1991          39          865-870
Studies on the Constituents of the Bark of Kalopanax pictus NAKAI
Kazuko SANO,Shuichi SANADA,Yoshiteru IDA and Junzo SHOJI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     HN-saponin H
    ÏàËÆ¶È:87.5%
Chemical & Pharmaceutical Bulletin          1985          33          3324-3329
Studies on Nepalese Crude Drugs. III. On the Saponins of Hedera nepalensis K. KOCH.
HARUHISA KIZU,SHINGO KITAYAMA,FUKIO NAKATANI,TSUYOSHI TOMIMORI and TSUNEO NAMBA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     glycoside pair f2
    ÏàËÆ¶È:87.5%
Chemistry of Natural Compounds          2006          42          61-66
TRITERPENE GLYCOSIDES FROM Kalopanax septemlobum.VII. MINOR GLYCOSIDES FROM STEMS OF Kalopanax septemlobumVAR. maximowiczii AND Kalopanax septemlobum VAR. typicum
D. A. Panov, V. I. Grishkovets, V. V. Kachala, and A. S. Shashkov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     spinoside C1
    ÏàËÆ¶È:87.5%
Phytochemistry          1997          46          1255-1259
3¦Á-hydroxy-oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus
Masazumi Miyakoshi, Susumu Isoda, Hirotoshi Sato, Yasuaki Hirai, Junzo Shoji, Yoshiteru Ida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

19 .     compound 3b
    ÏàËÆ¶È:87.5%
Acta Pharmaceutica Sinica          2000          Vol 35          821-825
NEW TRITERPENOID SAPONINS FROM ANEMONE BEGONIIFOLIA
LIAO Xun; LI Bo gong; DING Li sheng; PAN Yuan jiang; CHEN Yao zu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

20 .     Spinoside C1
C48H78O18     ÏàËÆ¶È:87.5%
Phytochemistry          1993          34          1599-1602
3¦Á-Hydroxy-oleanane-type triterpene glycosyl esters from leaves of Acanthopanax spinosus
Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

21 .     tragopogonoside C methyl ester
C48H76O19     ÏàËÆ¶È:87.5%
Phytochemistry          1992          31          2087-2091
Tragopogonosides A-I, oleanane saponins from Tragopogon pratensis
Toshio Miyase, Hiromi Kohsaka, Akira Ueno
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

22 .     pulsatiloside C
C48H78O18     ÏàËÆ¶È:87.5%
Phytochemistry          1990          29          595-599
Triterpenoid saponins from Pulsatilla campanella
Xing-Cong Li,De-Zu Wang,Su-Gong Wu,Chong-Ren Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

23 .     Hederagenin 28-O-¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl(1¡ú6)-¦Â-D-glucopyranoside
C48H78O18     ÏàËÆ¶È:87.5%
Chinese Pharmaceutical Journal          1996          31          522-524
GlycosidesintheleavesofOplopanaxelatus
NakaiWangGuangshu(WangGS), MengQin(MengQ), XuJingda(XuJD), etal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

24 .     umbellatoside A
C48H76O19     ÏàËÆ¶È:87.5%
Helvetica Chimica Acta          2011          94          1850-1859
New Triterpenoid and Ergostane Glycosides from the Leaves of Hydrocotyle umbellata L.
Adakarleny Sosa, Carmelo Rosquete, Luis Rojas, Laurent Pouys¨¦gu, St¨¦phane Quideau, Thomas Paululat, Anne-Claire Mitaine-Offer and Marie-Aleth Lacaille-Dubois
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

25 .     Hederagenin 28-O-[¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl-(1¡ú6)] ¦Â-D-glucopyranoside
C48H78O18     ÏàËÆ¶È:87.5%
Natural Product Communications          2006          1          27-32
Clarification of the Saponin Composition ofRanunculus ficaria Tubers
Andrew Marston, Martine Cabo, Christian Lubrano, Jean-Renaud Robin,Claude Fromageot and Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

26 .     scheffleroside II
    ÏàËÆ¶È:87.5%
West China Journal of Pharmaceutical Sciences          1990          5          132-135
Studies on saponins isolated from Schettlera Delavayi Harms ex diels
Jian qenpen, Xian Zhuoyin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

27 .     Yemuoside YM18
C47H76O19     ÏàËÆ¶È:87.2%
Helvetica Chimica Acta          2008          Vol. 91          451
Unusual Nortriterpenoid Saponins from Stauntonia chinensis
Hao Gao, ZhaoWang, Zhi-Hong Yao, NingWu, Hua-Jin Dong, Jin Li, Nai-LiWang, Wen-Cai Ye, and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

28 .     aralia-saponin I
C47H76O18     ÏàËÆ¶È:87.2%
Chemical & Pharmaceutical Bulletin          2000          48(6)          838-842
Four New Saponins from the Root Bark of Aralia elata
Shao-jiang SONG,Norio NAKAMURA,Chao-mei MA,Masao HATTORI and Sui-xu XU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

29 .     oleanolic acid 28-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-[¦Â-D-xylopyranosyl (1¡ú6)]-¦Â-D-glucopyranosyl ester
C47H76O16     ÏàËÆ¶È:87.2%
Archives of Pharmacal Research          2007          30          1-7
Antioxidant constituents and a new triterpenoid glycoside fromFlos Lonicerae
Chun-Whan Choi, Hyun Ah Jung, Sam Sik Kang and Jae Sue Choi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

30 .     rotundioside K
C48H77O22S     ÏàËÆ¶È:85.4%
Chemical & Pharmaceutical Bulletin          2006          54(12)          1694-1704
Antiproliferative Constituents from Umbelliferae Plants. IX.New Triterpenoid Glycosides from the Fruits of Bupleurum rotundifolium
Toshihiro FUJIOKA,Keisuke YOSHIDA, Hiroko SHIBAO, Tsuneatsu NAGAO, Miyako YOSHIDA,Kazuhisa MATSUNAGA, Jiro TAKATA, Yoshiharu KARUBE, Yukiko IWASE,Hikaru OKABE, and Kunihide MIHASHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

31 .     Acanjaposide D
C48H76O20     ÏàËÆ¶È:85.4%
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
--------------------------------------------------------------------------------

32 .     Acanjaposide F
C48H76O20     ÏàËÆ¶È:85.4%
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
--------------------------------------------------------------------------------

33 .     eclalbasaponin IV
C42H68O14     ÏàËÆ¶È:85.4%
Chemical & Pharmaceutical Bulletin          1994          42          1336-1338
Oleanane Glycosides from Eclipta alba
Shoji YAHARA,Ning DING and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

34 .     cirensenoside O
C48H78O17     ÏàËÆ¶È:85.4%
Acta Pharmaceutica Sinica          1996          31          940-944
ISOLATION AND STRUCTURE ELUCIDATION OF CIRENSENOSIDES O AND P FROM THE LEAVES OF OPLOPANAX ELATUS NAKAL
GS Wang; YP Chen; JD Xu; T Murayama and J Shoji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

35 .     spinoside C4
    ÏàËÆ¶È:85.4%
Phytochemistry          1997          46          1255-1259
3¦Á-hydroxy-oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus
Masazumi Miyakoshi, Susumu Isoda, Hirotoshi Sato, Yasuaki Hirai, Junzo Shoji, Yoshiteru Ida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

36 .     spinoside C5
    ÏàËÆ¶È:85.4%
Phytochemistry          1997          46          1255-1259
3¦Á-hydroxy-oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus
Masazumi Miyakoshi, Susumu Isoda, Hirotoshi Sato, Yasuaki Hirai, Junzo Shoji, Yoshiteru Ida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

37 .     hederagenin 28-O-¦Á-L-rhamnopyranosyl (1¡ú4)-¦Â-D-glucopyranosyl (1¡ú6)-¦Â-D-glucopyranosyl ester
    ÏàËÆ¶È:85.4%
Acta Pharmaceutica Sinica          2007          Vol 42          862-866
Triterpene glycosides from the aerial parts of Pulsatilla chinensis
SHI Bao-jun; Li Qian; ZHANG Xiao-qi; WANG Ying; YE Wen-cai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

38 .     kizuta saponin K3
    ÏàËÆ¶È:85.4%
Phytochemistry          1995          38          1473-1479
Triterpenoid saponins from Clematis chinensis
Baoping Shao, Guowei Qin, Rensheng Xu, Houming Wu, Kan Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

39 .     PS-3
    ÏàËÆ¶È:85.4%
Phytochemistry          1993          33          83-86
Molluscicidal and antifungal triterpenoid saponins from Rapanea melanophloeos leaves
Kazuhiro Ohtani, Steven Mavi, Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

40 .     hederagenin 28-O-[¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl (1¡ú6)-¦Â-D-glucopyranosyl] ester
    ÏàËÆ¶È:85.4%
Phytochemistry          1993          33          1469-1473
Triterpenoid glycosides from Stauntonia hexaphylla
Huai-Bin Wang, Ralf Mayer, Gerhard R¨¹cker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

41 .     Spinoside C5
C48H78O19     ÏàËÆ¶È:85.4%
Phytochemistry          1993          34          1599-1602
3¦Á-Hydroxy-oleanane-type triterpene glycosyl esters from leaves of Acanthopanax spinosus
Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

42 .     tragopogonoside D methyl ester
C48H76O19     ÏàËÆ¶È:85.4%
Phytochemistry          1992          31          2087-2091
Tragopogonosides A-I, oleanane saponins from Tragopogon pratensis
Toshio Miyase, Hiromi Kohsaka, Akira Ueno
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

43 .     heragenin 28-O-¦Á-L-rhamnopyranosyl(¡ú4)-¦Â-D-glucopyranosyl(1¡ú6)-¦Â-D-glucopyranosyl ester]
    ÏàËÆ¶È:85.4%
Chinese Traditional and Herbal Drugs          2008          39          819-822
Ð˰²°×Í·Î̸ù¾¥µÄ»¯Ñ§³É·ÖÑо¿
Ëï»Ô;ÀîÜç;Ò¶ÎIJÅ;ÕÔÊØÑµ;Ò¦ÐÂÉú
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

44 .     congmuyenoside I
C48H78O19     ÏàËÆ¶È:85.4%
Food Chemistry          2013          138          208-213
Studies on cytotoxic triterpene saponins from the leaves of Aralia elata
Yan Zhang, Ying Peng, Lingzhi Li, Lei Zhao, Yan Hu, Chong Hu, Shaojiang Song
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

45 .     ecliptasaponin B
C48H78O19     ÏàËÆ¶È:85.4%
Food Chemistry          2013          138          208-213
Studies on cytotoxic triterpene saponins from the leaves of Aralia elata
Yan Zhang, Ying Peng, Lingzhi Li, Lei Zhao, Yan Hu, Chong Hu, Shaojiang Song
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

46 .     centellasaponin D
C48H78O19     ÏàËÆ¶È:85.4%
Chemical & Pharmaceutical Bulletin          2011          49          1368-1371
Medicinal Foodstuffs. XXVII.1) Saponin Constituents of Gotu Kola (2):Structures of New Ursane- and Oleanane-Type Triterpene Oligoglycosides,Centellasaponins B, C, and D, from Centella asiaticaCultivated in Sri Lanka
Hisashi MATSUDA, Toshio MORIKAWA, Hiroki UEDA, and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

47 .     compound 5
C48H78O19     ÏàËÆ¶È:85.4%
Natural Medicines          2001          55          134-138
Five New Triterpene Glycosides from Centella asiatica
KURODA Minpei,MIMAKI Yoshihiro, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

48 .     compound 6
C48H78O19     ÏàËÆ¶È:85.4%
Natural Medicines          2001          55          134-138
Five New Triterpene Glycosides from Centella asiatica
KURODA Minpei,MIMAKI Yoshihiro, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

49 .     kalopanaxsaponin G
    ÏàËÆ¶È:85.4%
Chinese Traditional and Herbal Drugs          2012          43          2141-2145
Study on glycosides from stems of Schefflera kwangsiensis
ZHANG Qiao; SHEN Juan; ZHAO Yi-wu; WANG Zhen-zhong; XIAO Wei;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

50 .     centellasaponin D
C48H78O19     ÏàËÆ¶È:85.4%
Chemical & Pharmaceutical Bulletin          2001          49          1368-1371
Medicinal Foodstuffs. XXVII. Saponin Constituents of Gotu Kola (2): Structures of New Ursane- and Oleanane-Type Triterpene Oligoglycosides, Centellasaponins B, C, and D, from Centella asiatica Cultivated in Sri Lanka
Hisashi MATSUDA, Toshio MORIKAWA, Hiroki UEDA, Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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