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15.64, 16.51, 17.48, 18.48, 18.78, 19.50, 23.42, 23.82, 25.91, 28.15, 28.72, 29.94, 31.34, 33.11, 37.36, 38.96, 39.34, 39.89, 40.27, 40.52, 42.06, 42.37, 46.79, 48.06, 51.74, 55.77, 61.31, 69.30, 70.30, 70.90, 72.54, 72.75, 73.84, 73.99, 75.28, 76.51, 77.16, 78.00, 78.06, 78.31, 78.72, 95.74, 102.74., 104.93, 123.5, 143.31, 176.08, 178.48
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²éѯ½á¹û£º¹²²éµ½5408¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     Yemuoside YM20
C48H78O18     ÏàËÆ¶È:91.6%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     Yemuoside YM18
C47H76O19     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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     Yemuoside YM17
C47H76O19     ÏàËÆ¶È:87.5%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     Acanjaposide D
C48H76O20     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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     cussonside B
C48H78O17     ÏàËÆ¶È:87.5%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     Spinoside D3
C48H76O20     ÏàËÆ¶È:87.5%
Phytochemistry          1993          33          891-895
3-epi-Oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus
Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     spinoside D3
    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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     Oleanolic acid 28-O-[¦Á-Lrhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl-(1¡ú6)] ¦Â-D-glucopyranoside
C48H78O17     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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     yiyeliangwanoside XI
    ÏàËÆ¶È:86.7%
Phytochemistry          1995          38          695-698
Triterpenoid saponins from the bark of Nothopanax davidii
Shi Shan Yu, De Quan Yu, Xiao Tian Liang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     nipponoside D
    ÏàËÆ¶È:85.4%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     nipponoside D
C48H78O19     ÏàËÆ¶È:85.4%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     tauroside J
    ÏàËÆ¶È:85.4%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     tauroside I
    ÏàËÆ¶È:85.4%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     Durantanin IV
C48H78O20S     ÏàËÆ¶È:85.4%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     oleanolic acid 28-O-¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glccopyranosyl(1¡ú6)-¦Â-D-glccopyranosyl
    ÏàËÆ¶È:85.4%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     Spinoside D1
C48H76O19     ÏàËÆ¶È:85.4%
Phytochemistry          1993          33          891-895
3-epi-Oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus
Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     Spinoside D2
C48H74O20     ÏàËÆ¶È:85.4%
Phytochemistry          1993          33          891-895
3-epi-Oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus
Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     spinoside D1
    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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     spinoside D2
    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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     liangwanoside II
C53H84O23     ÏàËÆ¶È:84.9%
Chemical & Pharmaceutical Bulletin          1987          35          1486-1490
Saponins from Chinese Folk Medicine, ¡°Liang Wang Cha, ¡± Leaves and Stems of Nothopanax delavayi, Araliaceae
RYOJI KASAI,TOSHIHIKO OINAKA,CHONG-REN YANG,JUN ZHOU and OSAMU TANAKA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     liangwanoside II
    ÏàËÆ¶È:84.9%
Journal of Chinese Pharmaceutical Sciences          1995          4          167-176
Triterpenoid Saponins from the Bark of Nothopanaxdavidii
Shi-Shan; Yu; De-Quan Yu; Xiao-Tian Liang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
22 .     Acanjaposide E
C48H76O20     ÏàËÆ¶È:83.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
23 .     Acanjaposide I
C48H74O20     ÏàËÆ¶È:83.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
24 .     spinoside C1
    ÏàËÆ¶È:83.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
25 .     spinoside C2
C48H76O19     ÏàËÆ¶È:83.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
26 .     spinoside C4
    ÏàËÆ¶È:83.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
27 .     Spinoside C1
C48H78O18     ÏàËÆ¶È:83.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
28 .     Spinoside C5
C48H78O19     ÏàËÆ¶È:83.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
29 .     Glycoside C(3-epi-hederagenin)
C48H78O18     ÏàËÆ¶È:83.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
30 .     akemisaponin J
C47H74O18     ÏàËÆ¶È:83.3%
Chemical & Pharmaceutical Bulletin          2012          60          1264-1274
Triterpene Saponins from the Pericarps of Akebia trifoliata
Syuji Iwanaga, Tsutomu Warashina, Toshio Miyase
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
31 .     Compound 2a
    ÏàËÆ¶È:81.6%
Journal of Natural Medicines          2006          60          49-53
Triterpenoid saponins from cultural plants of Stenocereus stellatus (Cactaceae)
Takeo Imai, Sachie Okazaki, Kaoru Kinoshita, Kiyotaka Koyama and Kunio Takahashi, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
32 .     Yemuoside YM19
C47H74O18     ÏàËÆ¶È:81.2%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
33 .     Acanjaposide F
C48H76O20     ÏàËÆ¶È:81.2%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
34 .     Acanjaposide H
C48H76O19     ÏàËÆ¶È:81.2%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
35 .     acanjaposide A
C47H72O19     ÏàËÆ¶È:81.2%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
36 .     nipponoside A
C48H76O18     ÏàËÆ¶È:81.2%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
37 .     cynarasaponin J methyl ester
C48H76O19     ÏàËÆ¶È:81.2%
Chemical & Pharmaceutical Bulletin          1988          36          2466-2474
Sesquiterpene Glycosides and Saponins from Cynara cardunculus L.
SHIGERU SHIMIZU,NAOMI ISHIHARA,KAORU UMEHARA,TOSHIO MIYASE and AKIRA UENO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
38 .     spinoside C5
    ÏàËÆ¶È:81.2%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
39 .     compound 7
    ÏàËÆ¶È:81.2%
Acta Pharmaceutica Sinica          2004          Vol 39          354-358
Structures of four new triterpenoid saponins from the leaves of Oplopanax elatus Nakai
WANG Guang-shu; YANG Xiao-hong; XU Jing-da
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
40 .     3-O-¦Á-L-RhamnopyranosyL(1¡ú3)-¦Â-D-glucopyranosyl-28-O-¦Â-D-glucopyranosyl oleanolic acid
    ÏàËÆ¶È:81.2%
Phytochemistry          1995          40          1765-1767
Triterpenoidal saponins from Dumasia Truncata
Junei Kinjo, Kumi Suyama, Toshihiro Nohara
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
41 .     Spinoside C4
C48H76O19     ÏàËÆ¶È:81.2%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
42 .     oleunolic acid 3-0-(3'-0-¦Á-L-rhamnopyranosyl)-¦Â-D-glucuronopyranoside-28-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:81.2%
Phytochemistry          1984          23          2907-2910
Two saponins from Zexmenia buphthalmiflora
Claudio D. Schteingart, Alicia B. Pomilio
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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