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16.9,17.1,19.3,23.0,23.7,23.8,23.9,27.6,30.9,32.5,33.1,33.2,33.8,37.9,39.4,41.3,41.7,43.4,45.9,46.2,47.4,47.8,56.8,64.3,84.3,121.8,130.1,134.0,144.3,165.3,179.1
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1 .     2¦Á,3¦Á,24-ÈýôÇ»ù-12-Ï©-28-Æë¶Õ¹ûËá
C30H48O5     ÏàËÆ¶È:83.8%
Chinese Pharmaceutical Journal          2001          36          445-447
Studies on the chemical constituents of Callicarpa bodinieri (¢ò)
REN Feng zhi, LUAN Xin hui, QU Hui hua, ZHAO Yi min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     2¦Á,3¦Â,24-trihydroxyolean-12-en-28-oate
C31H50O5     ÏàËÆ¶È:83.8%
The Journal of Organic Chemistry          2007          72          3500-3509
Remote Hydroxylation of Methyl Groups by Regioselective Cyclopalladation. Partial Synthesis of Hyptatic Acid-A
Andr¨¦s Garc¨ªa-Granados, Pilar E. L¨®pez, Enrique Melguizo, Andr¨¦s Parra, and Yolanda Sime¨®
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     methyl 2¦Á,3¦Â,24-trihydroxy-olean-12-en-28-oate
    ÏàËÆ¶È:83.8%
Indian Journal of Chemistry          2002          41B          234-236
Triterpene and triterpene glycosides from Salvia tricupis
Zhen-Fu Hou, Zhi-Xiang Xie, Yong-Qiang Tu & Yu Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     olean-12-en-28-oic acid 3¦Â,24-diol
    ÏàËÆ¶È:80.6%
Chemical & Pharmaceutical Bulletin          1982          30          3340-3346
Studies on the Constituents of Clematis Species. V. On the Saponins of the Root of Clematis chinensis OSBECK. (5)
HARUHISA KIZU and TSUYOSHI TOMIMORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     Maslinic acid
C30H48O4     ÏàËÆ¶È:80.6%
Chemistry of Natural Compounds          2009          45          921-924
ISOPRENOIDS OF Euphorbia sororia. I. TRITERPENOIDS
Y. Huang,H. A. Aisa, and M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     4-epihederagenin
    ÏàËÆ¶È:80.6%
Chemistry of Natural Compounds          1992          28          1-23
13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES
A. I. Kalinovskii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     2¦Á,3¦Á,24-trihydroxyolean-12-en-28-oic acid
    ÏàËÆ¶È:80.6%
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
8 .     3¦Â,16¦Á,24-OH oleanlic acid
    ÏàËÆ¶È:80.6%
Acta Pharmaceutica Sinica          1999          Vol 34          679-681
STUDIES ON THE CHEMICAL CONSTITUENTS FROM PRUNELLA VULGARIS
Wang Zhuju (Wang ZJ); Zhao Yuying (Zhao YY); Tu Guangzhong (Tu GZ); Hong Shaoliang (Hong SL) and Chen Yayan (Chen YY)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     epihedaragenin
    ÏàËÆ¶È:80.6%
Phytochemistry          1994          37          1517-1575
13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features
Shashi B. Mahato, Asish P. Kundu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     4-epi-hederagenin
    ÏàËÆ¶È:80.6%
Korean Journal of Pharmacognosy          1987          18(3)          151-167
13C NMR Spectroscopy of Amyrins
Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     2¦Á,3¦Â,24-ÈýôÇ»ù-12-Ï©-28-Æë¶Õ¹ûËá(2¦Á,3¦Â,24-trihydroxy-olea-12-en-28-oic acid)
    ÏàËÆ¶È:80.6%
Chinese Traditional and Herbal Drugs          2011          42(5)          859-862
Chemical constituents of Salvia plebaia
LU Ru-mei, YANG Chang-shui, WEI Jian-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     maslinatic acid
C30H48O4     ÏàËÆ¶È:80.6%
Chinese Traditional and Herbal Drugs          2000          31          409-412
Triterpenes from Butter-and-Eggs (Linaria vulgaris)
Shenyang Pharmaceutical University (Shenyang )Hua Huiming; Hou Bailing; Li Wen and Li Xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     2¦Á,3¦Â,24-trihydroxy olean-12-en-28-oic acid
    ÏàËÆ¶È:80.6%
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
14 .     2¦Á,3¦Â,24-Trihydroxyolea-12en-28oic acid
    ÏàËÆ¶È:80.6%
Archives of Pharmacal Research          2008          31          1578-1583
Triterpenoic acids of Prunella vulgaris var. lilacina and their cytotoxic activities In Vitro
Il Kyun Lee, Do Hoon Kim, Seung Young Lee, Kyung Ran Kim and Sang Un Choi, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     maslinic acid
    ÏàËÆ¶È:80.6%
Chinese Pharmaceutical Journal          2003          38          752-757
Studies on constituents of triterpene acids from Eriobotrya japonica and their anti-inflammatory and antitussive effects
JU Jian-hua, ZHOU Liang, LIN Geng, LIU Dong, WANG Li-wei, YANG Jun-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     maslinic acid
C30H48O4     ÏàËÆ¶È:80.6%
Natural Product Research and Development          2009          21          608-611
Chemical Constituents of Clerodendranthus spicatus
TAN Jun-jie; TAN Chang-heng; CHEN Yi-lei; JIANG Shan-hao; ZHU Da-yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     ÐܹûËáÒÒõ¥
    ÏàËÆ¶È:80.6%
Natural Product Research and Development          2007          19          51-54
Study on Nonirodoids from Fruits of Lonicera maackii
WANG Yu-li; YANG Li; LUO Guo-an; WANG Yi-ming*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     2¦Á,3¦Á,24-trihydroxyolean-12-en-28-oic acid
C30H48O5     ÏàËÆ¶È:80.6%
Academic Journal of Second Military Medical University          2011          32          749-753
Anti-tumor constituents from the roots of Actinidia valvata
XU Yi-xin, XIANG Zhao-bao, CHEN Xiao-jing, CHEN Hai-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     2¦Á,3¦Á,24-trihydroxy-olea-12-en-28-oic acid
    ÏàËÆ¶È:80.6%
Chinese Traditional and Herbal Drugs          2012          43          861-865
Chemical constituents from whole herb of Hedyotis scandens
DENG Fang-ye; WANG Guo-cai; WANG Chun-hua; YE Wen-cai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     2¦Á,3¦Â-dihydroxyolean-12-ene-24,28-dioic acid dimethyl ester
C32H50O6     ÏàËÆ¶È:78.1%
Planta Medica          2003          69          327-331
A New in vitro Tissue Factor Inhibitory Triterpene from the Fruits of Chaenomeles sinensis
Ming Hong Lee,Yong Nam Han
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     2¦Á-Hydroxyolean-12-en-28-oic acid
C30H48O3     ÏàËÆ¶È:77.4%
Journal of Natural Products          2009          72          1414-1418
Synthesis of 3-Deoxypentacyclic Triterpene Derivatives as Inhibitors of Glycogen Phosphorylase
Pu Zhang,Jia Hao,Jun Liu,Qian Lu, Huaming Sheng, Luyong Zhang, and Hongbin Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     methyl arjunolate
    ÏàËÆ¶È:77.4%
Planta Medica          1990          56          287-289
Further Triterpenoids of Musanga cecropioides:The Structure of Cecropic Acid
D. Lontsi, B. L. Sondengam, J. F. Ayafor, M G. Tsoupras, andR. Tabacchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     Hedera
    ÏàËÆ¶È:77.4%
Acta Botanica Yunnanica          2000          22(2)          201-208
Triterpenoid Glycosides from the Lonicera japonica
CHEN Chang-Xiang,WANGWei-Wei,NI Wei,CHEN Neng-Yu,ZHOU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     compound 2b
    ÏàËÆ¶È:77.4%
Chemical & Pharmaceutical Bulletin          1992          40          401-405
Studies on Differentiation-Inducing Activities of Triterpenes
Kaoru UMEHARA,Rieko TAKAGI,Masanori KUROYANAGI,Akira UENO,Takao TAKI and Ying-Jie CHEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     compound 2
    ÏàËÆ¶È:77.4%
Chemical & Pharmaceutical Bulletin          1989          37          1770-1775
Studies on the Constituents of Actinostemma lobatum MAXIM. IV. Structures of Lobatosides C, D and H, the Dicrotalic Acid Esters of Bayogenin Bisdesmosides Isolated from the Herb
Toshihiro FUJIOKA,Masayo IWAMOTO,Yukiko IWASE,Shizuko HACHIYAMA,Hikaru OKABE,Tatsuo YAMAUCHI and Kunihide MIHASHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     oleanolic acid acid 3-O-sulfate
    ÏàËÆ¶È:77.4%
Chemical & Pharmaceutical Bulletin          1985          33          3715-3723
Sulfated Triterpenoid Saponins from the Leaves of Bupleurum rotundifolium L.
ERIKO AKAI,TADAHIRO TAKEDA,YOSHIMASA KOBAYASHI and YUKIO OGIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     compound 7
C30H47O6S-0.5Ca-3.5H2O     ÏàËÆ¶È:77.4%
Chemical & Pharmaceutical Bulletin          1985          33          3715-3723
Sulfated Triterpenoid Saponins from the Leaves of Bupleurum rotundifolium L.
ERIKO AKAI,TADAHIRO TAKEDA,YOSHIMASA KOBAYASHI and YUKIO OGIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     ST-D2
    ÏàËÆ¶È:77.4%
Chemistry of Natural Compounds          1997          33          316-319
TRITERPENE GLYCOSIDES OF Hedera taurica XVI. STRUCTURES OF GLYCOSIDES St-A, St-B 1, St-B 2, St-C,St-D1, St-D2, St-E, St-F 1, AND St-F 2 FROM THE STEMS OF CRIMEAN IVY
V. I. GriShkovets, S. V. Godin, O. Ya. Tsvetkov,A. S. Shamhkov, and V. Ya. Chirva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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