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16.39,17.26,17.51,18.85,23.49,23.79,23.90,24.58,28.51,32.40,33.92,37.47,38.50,40.30,42.50,43.24,45.12,48.08,48.47,49.44,55.30,62.28,65.16,66.20,71.13,73.93,74.20,78.80,79.19,79.75,95.74,105.20,126.35,138.03,153.18,175.63
  
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cj¿¼ÑÐ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл£¡ÐÁ¿àÀ²£¡ 2012-06-12 14:13:33
1 .     2¦Á,3¦Á,24-trihydroxyurs-12-en-28-oic acid-28-O-¦Â-D-glucopyranosyl ester
C36H58O10     ÏàËÆ¶È:83.3%
Chemical & Pharmaceutical Bulletin          2004          52(1)          157-159
A New Pentacyclic Triterpenoid Glucoside from Prunus serrulata var. spontanea
Hyun Ah JUNG,Hae Young CHUNG,Jee H. JUNG,and Jae Sue CHOI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (2¦Â,3¦Á)-2,3,20,23,24,30-hexahydroxyurs-12-en-28-oic acid O-¦Â-D-glucopyranosyl ester
C36H58O13     ÏàËÆ¶È:77.7%
Helvetica Chimica Acta          2008          Vol. 91          575
Two New Polyoxygenated Triterpenoids from Actinidia valvata
Hai-Liang Xin, Xiao-Qiang Yue, Yan-Feng Xu, Ying-Chun Wu, Ya-Ni Zhang, Yong-Zi Wang, and Chang-Quan Ling
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     2¦Á,3¦Á,19¦Á,24-tetrahydroxyurs-12-en-28-oic acid-28-O-¦Â-D-glucopyranosyl ester
C36H58O11     ÏàËÆ¶È:77.7%
Chemical & Pharmaceutical Bulletin          2004          52(1)          157-159
A New Pentacyclic Triterpenoid Glucoside from Prunus serrulata var. spontanea
Hyun Ah JUNG,Hae Young CHUNG,Jee H. JUNG,and Jae Sue CHOI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     2¦Á,3¦Â,23-trihydroxyurs-12-en-28-oic acid O-¦Â-D-glucopyranosyl ester
    ÏàËÆ¶È:77.7%
Acta Pharmaceutica Sinica          2006          Vol 41          835-839
A new triterpenoid saponin from stems of Akebia trifoliata
GAO Hui-min; WANG Zhi-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     vulgarsaponin A
    ÏàËÆ¶È:77.7%
Acta Pharmaceutica Sinica          2000          Vol 35          29-31
STRUCTURE IDENTIFICATION OF VULGARSAPONIN A
Tian Jing; Xiao Zhiyan; Chen Yayan; Zhao Yuying and Wang Zhuju
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     2¦Á,3¦Á,19¦Á,24-tetrahydroxyurs-12-en-28-oic acid ¦Â-D-glucopyranosyl ester
    ÏàËÆ¶È:77.7%
Journal of Natural Medicines          2009          63          318-322
A new diterpenoid and a new triterpenoid glucosyl ester from the leaves of Callicarpa japonica Thunb. var. luxurians Rehd.
Masateru Ono, Tomoyo Chikuba, Kenji Mishima, Toru Yamasaki and Tsuyoshi Ikeda, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     2¦Á,3¦Á,19¦Á,24-tetrahydroxyurs-12-en-28-oic acid 28-O-¦Â-Dglucopyranoside
    ÏàËÆ¶È:77.7%
Fitoterapia          2010          81          920-924
Two new triterpenoids from the roots of Actinidia chinensis
Yi-Xin Xu, Zhao-Bao Xiang, Yong-Sheng Jin, Yang Shen, Hai-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     cincholic acid 28-O-¦Â-glucopyranosyl ester
C36H56O10     ÏàËÆ¶È:75%
Planta Medica          2005          71          355-361
Six New Triterpenoid Saponins from the Root and Stem Bark of Cephalanthus occidentalis
Zhang, Zhizhen; Li, Shiyou; Zhang, Shanmin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     Quadranoside IV
    ÏàËÆ¶È:75%
Molecules          2008          13          2717-2728
Bioactive Pentacyclic Triterpenes from the Stems of Combretum laxum
Eder Bisoli, Walmir S. Garcez, Lidilhone Hamerski, Caroline Tieppo and Fernanda R. Garcez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     2¦Á,3¦Á,24-trihydroxyursa-12,20(30)-dien-28-oic acid
    ÏàËÆ¶È:75%
Journal of Chinese Pharmaceutical Sciences          2000          9          128-130
A New Phenylpropanoid and Triterpenoids from Prunella vulgaris
Wang Zhuju, Zhao Yuying, Wang Bin, Li Jiexiu, Ai Tiemin and Chen Yayan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     2¦Á,3¦Á,19¦Á,24-tetrahydroxyurs-12-en-28-oic acid-28-O-¦Â-D-glucopyranosyl ester
C36H58O11     ÏàËÆ¶È:75%
Phytochemistry          1998          49          2477-2481
Pentacyclic triterpenoids from Rubus xanthocarpus
Bao-Zhi Li, Bin-Gui Wang, Zhong-Jian Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     2¦Á,3¦Á,19¦Á,23-tetrahydroxy-ursa-12-en-28-oic acid-28-O-¦Â-D-glucopyranosyl ester
    ÏàËÆ¶È:75%
China Journal of Chinese Materia Medica          2010          35          3297-3301
Chemical constituents from Callicarpa nudiflora and their hemostatic acitivity
ZHANG Jie; LI Baoquan; FENG Feng; TANG Yuping; LIU Wenyuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     2¦Á,3¦Á,23-trihydroxy-urs-12-en-28-oic acid 28-O-¦Â-D-glucopyranoside
C36H58O10     ÏàËÆ¶È:75%
Bioorganic & Medicinal Chemistry Letters          2012          22          2079-2083
Cytotoxic terpenoids from Juglans sinensis leaves and twigs
Heejung Yang, Hyun-Jong Cho, So Hee Sim, Young Keun Chung, Dae-Duk Kim, Sang Hyun Sung, Jinwoong Kim, Young Choong Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     3¦Â,23-Dihydroxyurs-12-en-28-oic acid 28-O-¦Â-D-glucopyranoside
C36H58O9     ÏàËÆ¶È:75%
Journal of Natural Products          2011          74          751-756
Antiproliferative Triterpenes from the Leaves and Twigs of Juglans sinensis on HSC-T6 Cells
Heejung Yang, Eun Ju Jeong, Jinwoong Kim, Sang Hyun Sung, and Young Choong Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     callianthaside A
C36H58O11     ÏàËÆ¶È:72.2%
Helvetica Chimica Acta          2007          Vol. 90          2421
Phenolic and Triterpenoid Glycosides from Pyrola calliantha
Yi-Lei Chen, Chang-Heng Tan, Jun-Jie Tan, Shi-Jin Qu, Heng-Bin Wang, Qiang Zhang, Shan-Hao Jiang, and Da-Yuan Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     rubuside E
C36H56O9     ÏàËÆ¶È:72.2%
Journal of Natural Products          2009          72          1755-1760
Triterpenoid Saponins from Rubus ellipticus var. obcordatus
Wei Li, Hongwei Fu, Hong Bai, Tatsunori Sasaki, Hiroyoshi Kato, and Kazuo Koike
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     rubuside H
C36H56O10     ÏàËÆ¶È:72.2%
Journal of Natural Products          2009          72          1755-1760
Triterpenoid Saponins from Rubus ellipticus var. obcordatus
Wei Li, Hongwei Fu, Hong Bai, Tatsunori Sasaki, Hiroyoshi Kato, and Kazuo Koike
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     (20S)-niga-ichigoside F1
C36H58O11     ÏàËÆ¶È:72.2%
Journal of Natural Products          2005          68          1531-1535
Phenolic and Triterpene Glycosides from the Stems of Ilex litseaefolia
Ai-Lian Zhang, Qi Ye, Bo-Gang Li, Hua-Yi Qi, and Guo-Lin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     quadranoside IV
C36H58O10     ÏàËÆ¶È:72.2%
Journal of Natural Products          2000          63          496-500
Quadranosides I-V, New Triterpene Glucosides from the Seeds of Combretum quadrangulare
I Ketut Adnyana, Yasuhiro Tezuka, Arjun H. Banskota, Quanbo Xiong, Kim Qui Tran, and Shigetoshi Kadota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     ¦Â-D-glucopyranosyl 2¦Á,3¦Â,23,24-tetrahydroxyurs-12-en-28-oate
    ÏàËÆ¶È:72.2%
Molecules          2008          13          2717-2728
Bioactive Pentacyclic Triterpenes from the Stems of Combretum laxum
Eder Bisoli, Walmir S. Garcez, Lidilhone Hamerski, Caroline Tieppo and Fernanda R. Garcez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     chebuloside II
    ÏàËÆ¶È:72.2%
Natural Product Research          2001          15          35-42
Vanillic Acid 4-O-¦Â-D-(6'-O-Galloyl) Glucopyranoside and Other Constituents from the Bark of Terminalia macroptera Guill. Et Perr
J¨¹rgen Conrad; Bernhard Vogler; Iris Klaiber; Sabine Reeb; Jan-Hinrich Guse; Gudrun Roos; Wolfgang Kraus
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     2¦Á,3¦Â,23-trihydroxyolean-12-en-28-oic acid O-¦Â-D-glucopyranosyl ester
    ÏàËÆ¶È:72.2%
Acta Pharmaceutica Sinica          2006          Vol 41          835-839
A new triterpenoid saponin from stems of Akebia trifoliata
GAO Hui-min; WANG Zhi-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     Alpinoside
C30H46O4     ÏàËÆ¶È:72.2%
Phytochemistry          1993          32          155-159
Triterpenoids from Sanguisorba alpina
Zhong-Jian Jia, Xiang-Qian Liu, Zi-Min Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     ilexoside XXXIV
C36H57O13SNa     ÏàËÆ¶È:72.2%
Phytochemistry          1993          33          1475-1480
Triterpenes and triterpene glycosides from the leaves of Ilex rotunda
Kayoko Amimoto, Kazuko Yoshikawa, Shigenobu Arihara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     2¦Á,3¦Á,19¦Á,24-tetrahydroxyolea-12-en-28-oic acid ¦Â-D-glu-copyranosyl ester
C36H58O11     ÏàËÆ¶È:72.2%
Journal of Natural Medicines          2009          63          318-322
A new diterpenoid and a new triterpenoid glucosyl ester from the leaves of Callicarpa japonica Thunb. var. luxurians Rehd.
Masateru Ono, Tomoyo Chikuba, Kenji Mishima, Toru Yamasaki and Tsuyoshi Ikeda, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     28-O-¦Â-D-glucopyranosyl oleanolic acid
C26H58O8     ÏàËÆ¶È:72.2%
Chinese Journal of Natural Medicines          2003          1          134-136
Triterpene and Saponins from Kochia scoparia
WANG Hao; FAN Chun-Lin; WANG Bei; DAI Yue; YE Wen-Cai; ZHAO Shou-Xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     2¦Á,3¦Â,23-trihydroxyurs-12-en-28-oic acid ¦Â-D-glucopyranosyl ester
    ÏàËÆ¶È:72.2%
Chinese Journal of Natural Medicines          2009          7          206-209
Triterpene Saponins from the Leaves of Ilex pernyi
XIE Guang-Bo; JIANG Yong; LEI Lian-Di; TU Peng-Fei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     2¦Á,3¦Á,19¦Á,24-tetrahydroxylurs-12-en-28-oic acid-28-¦Â-D-glucopranoside
    ÏàËÆ¶È:72.2%
Chinese Journal of Natural Medicines          2009          7          421-424
Triterpenes from Prunella vulgaris
QI Jin; HU Zheng-Fang; LIU Zhi-Jun; YU Bo-Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     2¦Á,3¦Â,19¦Á,24-tetrahydroxylurs-12-en-28-oic acid-28-¦Â-D-glucopranoside
    ÏàËÆ¶È:72.2%
Chinese Journal of Natural Medicines          2009          7          421-424
Triterpenes from Prunella vulgaris
QI Jin; HU Zheng-Fang; LIU Zhi-Jun; YU Bo-Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     2¦Á,3¦Â,7¦Á,23-tetrahydroxy-olean-12-en-28-oic acid 28-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:72.2%
Archives of Pharmacal Research          1997          20          291-296
Constituents of the herb of Isodon excisus var. coreanus
Ho Kyoung Kim, Wan Kyunn Whang and Il Hyuk Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     »ýÑ©²Ýµ¥ÌÇÜÕ
    ÏàËÆ¶È:72.2%
Modern Chinese Medicine          2008          10(3)          7-9
Chemical studies on the saponin compounds of Centella asiatica
Liu Yu, Zhao Yuqing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     rotungenoside
C36H58O10     ÏàËÆ¶È:72.2%
Bulletin of the Chemical Society of Japan          1989          62          469-473
The Structure of Rotungenoside, a New Bitter Triterpene Glucoside from Ilex Rotunda
Munehiro Nakatani, Shuichi Hatanaka, Hajime Komura, Takashi Kubota, Tsunao Hase
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     ilexoside A
    ÏàËÆ¶È:70.7%
Archives of Pharmacal Research          1987          10          132-141
New triterpenoid saponins fromIlex pubescens
Yong Nam Han, Seung Kyung Bail, Tae Hee Kim and Byung Hoon Han
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     2¦Á,3¦Á,19,24-ËÄôÇ»ù-12-Ï©-ÎÚËÕËá-28-O-¦Â-D-ÆÏÌÑÌÇõ¥
    ÏàËÆ¶È:70.2%
Chinese Pharmaceutical Journal          2004          39          17-19
Study on the chemical constituents of Callicarpa bodinieri
REN Feng zhi, HE Bing kun, LUAN Xin hui, ZHAO Yi min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     rubuside B
C36H56O9     ÏàËÆ¶È:69.4%
Journal of Natural Products          2009          72          1755-1760
Triterpenoid Saponins from Rubus ellipticus var. obcordatus
Wei Li, Hongwei Fu, Hong Bai, Tatsunori Sasaki, Hiroyoshi Kato, and Kazuo Koike
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     rubuside G
C36H56O9     ÏàËÆ¶È:69.4%
Journal of Natural Products          2009          72          1755-1760
Triterpenoid Saponins from Rubus ellipticus var. obcordatus
Wei Li, Hongwei Fu, Hong Bai, Tatsunori Sasaki, Hiroyoshi Kato, and Kazuo Koike
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     niga-ichigoside F1
    ÏàËÆ¶È:69.4%
Chemical & Pharmaceutical Bulletin          2003          51(2)          200-202
A New Triterpene Glucosyl Ester from the Fruit of the Blackberry (Rubus allegheniensis)
Masateru ONO,Michiko TATEISHI, Chikako MASUOKA,Hiromasa KOBAYASHI,Keiji IGOSHI,Haruki KOMATSU,Yasuyuki ITO,Masafumi OKAWA,and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     quadranoside VIII
C36H56O10     ÏàËÆ¶È:69.4%
Chemical & Pharmaceutical Bulletin          2000          48(8)          1114-1120
Quadranosides VI-XI, Six New Triterpene Glucosides from the Seeds of Combretum quadrangulare
I Ketut ADNYANA,Yasuhiro TEZUKA, Suresh AWALE,Arjun Hari BANSKOTA, Kim Qui TRAN and Shigetoshi KADOTA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     quadranoside X
C36H58O11     ÏàËÆ¶È:69.4%
Chemical & Pharmaceutical Bulletin          2000          48(8)          1114-1120
Quadranosides VI-XI, Six New Triterpene Glucosides from the Seeds of Combretum quadrangulare
I Ketut ADNYANA,Yasuhiro TEZUKA, Suresh AWALE,Arjun Hari BANSKOTA, Kim Qui TRAN and Shigetoshi KADOTA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     2¦Á,3¦Â,23-trihydroxyurs012,19-dien-28-oic acid 28-O-¦Â-D-glucopyranside
    ÏàËÆ¶È:69.4%
Chemical & Pharmaceutical Bulletin          2000          48(8)          1114-1120
Quadranosides VI-XI, Six New Triterpene Glucosides from the Seeds of Combretum quadrangulare
I Ketut ADNYANA,Yasuhiro TEZUKA, Suresh AWALE,Arjun Hari BANSKOTA, Kim Qui TRAN and Shigetoshi KADOTA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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