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1 .     3¦Â-hydroperoxy-7¦Â,25-epoxy-D:B-friedoolean-5-ene
C30H48O3     ÏàËÆ¶È:66.6%
Journal of Natural Products          2009          72          1045-1048
Triterpenoids and a Lignan from the Aerial Parts of Maytenus apurimacensis
Nabil E. J. Vazdekis, Haydee Ch¨¢vez, Ana Est¨¦vez-Braun, and ¨¢ngel G. Ravelo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     pomolic acid
    ÏàËÆ¶È:66.6%
Natural Product Sciences          2007          13          152-159
The Anti-hyperlipidemic Effect and Constituents of the 19-Hydroxyursane-type Triterpenoid fraction Obtained from the Leaves of Rusus crataegifolius
Nam, Jung-Hwan; Jung, Hyun-Ju; Tapondjou, Leon Azefack; Lee, Kyung-Tae; Choi, Jong-Won; Kim, Won-Bae; Park, Hee-Juhn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     ursolic acid
    ÏàËÆ¶È:66.6%
Chinese Traditional and Herbal Drugs          1999          30(3)          161-164
Studies on the Chemical Constituents of Shady Jerusalemsage (Phlomis umbrosa)(¢ñ)
Liu Shiwang; Fu Hongzheng and Lin Wenhan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     21¦Á-hydroxy ursolic acid
    ÏàËÆ¶È:66.6%
Natural Product Research and Development          1997          9(2)          4-6
NON-ALKALOIDAL CONSTITUENTS FROM MECONOPSIS PUNICEA MAXIM
Zhang Guolin; Li Bogang; Zhou Zhengzhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (23E)-25-methoxycucurbit-23-ene-3¦Â,7¦Â-diol
C31H52O3     ÏàËÆ¶È:64.5%
Journal of Natural Products          2006          69          1168-1171
Cucurbitane-Type Triterpenoids from Momordica charantia
Chi-I Chang, Chiy-Rong Chen, Yun-Wen Liao, Hsueh-Ling Cheng, Yo-Chia Chen, and Chang-Hung Chou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     20¦Â,28-epoxy-28¦Á-methoxytaraxasteran-3¦Â-ol
C31H52O3     ÏàËÆ¶È:64.5%
Journal of Natural Products          2006          69          1164-1167
Taraxasterane- and Ursane-Type Triterpenes from Nerium oleander and Their Biological Activities
Ming Zhao, Shujun Zhang, Liwei Fu, Na Li, Jiao Bai, Junichi Sakai, Liyan Wang, Wanxia Tang, Toshiaki Hasegawa, Hirotsugu Ogura, Takao Kataoka, Seiko Oka, Miwa Kiuch, Katutoshi Hirose, and Masayoshi Ando
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     21-dehydro-macedonic acid methyl ester
C31H46O4     ÏàËÆ¶È:64.5%
Acta Pharmaceutica Sinica          1990          Vol 25          795-797
ISOLATION AND IDENTIFICATION OF YIBEINOSIDE A
DM Xu; S Arihara; N Shoji; XW Yang; EX Huang and CS Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (3¦Â,18¦Á,19¦Á)-ursane-3,20,28-triol
C30H50O3     ÏàËÆ¶È:63.3%
Helvetica Chimica Acta          2006          Vol. 89          3018
Three New Triterpenoids from Dracocephalum forrestii
Gan-Peng Li, Jing-Feng Zhao, Li-Juan Yang , Xiao-Dong Yang, and Liang Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     aceriphyllic acid D
C30H46O5     ÏàËÆ¶È:63.3%
Journal of Natural Products          2009          72          1419-1423
Oleanane-Type Triterpenoids from Aceriphyllum rossii and Their Cytotoxic Activity
Le Thi Kim Van, Tran Manh Hung, Phuong Thien Thuong, Tran Minh Ngoc, Jin Cheol Kim, Han-Su Jang,Xing Fu Cai,Sei Ryang Oh, Byung-Sun Min, Mi Hee Woo,Jae Sue Choi, Hyeong Kyu Lee, and KiHwan Bea
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     gamboukokoensein A
C30H48O7     ÏàËÆ¶È:63.3%
Phytochemistry          2003                   845-849
Pentacyclic triterpenoid and saponins from Gambeya boukokoensis
Jean Wandji, François Tillequin, Dulcie A. Mulholland, Jovita Chi Shirri,Nole Tsabang, ElisabethSeguin, Philippe Verite, Francine Libotb, Z.T. Fomum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     cycloartan-23E-ene-1¦Á,2¦Á,3¦Â,25-tetrol
C30H50O4     ÏàËÆ¶È:63.3%
Journal of Natural Products          2008          71(1)          81-86
Cycloartane-Type Triterpenoids from the Resinous Exudates of Commiphora opobalsamum
Tao Shen, Hui-Qing Yuan, Wen-Zhu Wan, Xiao-Ling Wang, Xiao-Ning Wang, Mei Ji, and Hong-Xiang Lou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     29,30-dibromoallobetulin
C30H47O2Br2     ÏàËÆ¶È:63.3%
Chemistry of Natural Compounds          2006          42          186-188
SYNTHESIS AND CRYSTAL STRUCTURE OF 29,30-DIBROMOALLOBETULIN
M. Yu. Lezhneva, E. E. Schultz I. Yu. Bagryanskaya,Yu. V. Gatilov, M. M. Shakirov,G. A. Tolstikov, and S. M. Adekenov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     compound 1
    ÏàËÆ¶È:63.3%
Chemistry of Natural Compounds          1986          22          421-424
GLYCOSYLATION OF TRITERPENOIDS OF THE DAMMARANE SERIES. VI. 3-MONO- AND 3,12-DI-O-¦Â-D-GLUCOPYRANOSIDES OF PYXINOL
L. N. Atopkina-and N. I. Uvarova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     20(S),24(R)-epoxydammarane-3¦Â,12¦Â,25-triol
    ÏàËÆ¶È:63.3%
Chemistry of Natural Compounds          1982          18          546-571
CATALYTIC REARRANGEMENT OF 1,2 ORTHOACETATES OF ¦Á-D-GLUCOSE AND 20(S),24(R)-EPOXYDAMMARANE-3,123,25-TRIOLS. I.
N. F. Samoshina, L. N. Atopkina, V. L. Novikov, V. A. Denisenko, and N. I. Uvarova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     ursolic acid
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2003          28          527-531
Chemical Constituents from the Leaves of Dalbergia hainanensis
ZHANG Peicheng, WU Yan, YU Dequan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     19¦Á-hydroxyursolic acid
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          1996          21          427-428
Studies on the Chemical Constituents of the Root of Boehmeira nivea (L.) Gaud
Li Wenwu, Ding Liaheing and Li Bogang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     3¦Â,11¦Á-dihydroxytaraxer-14-en-12-one
C32H52O5     ÏàËÆ¶È:63.3%
Phytochemistry          2000          54          823-827
Two oleanane triterpenoids from Gordonia ceylanica and their conversions to taraxarane triterpenoids
H.M.T.B. Herath, P.S. Athukoralage, Joanne F. Jamie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     1¦Â,22¦Â-dihydroxyolean-11,13(18)-diene
C30H48O2     ÏàËÆ¶È:63.3%
Phytochemistry          1998          48          693-697
Saikosaponins from Taverniera aegyptiaca
H. A. Hassanean
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     3-epikatonic acid
C30H48O3     ÏàËÆ¶È:63.3%
Acta Pharmaceutica Sinica          1999          Vol 34          210-213
THE TRITERPENOIDS OF TRIPTERYGIUM WILFORDII
Guo Fujiang (Guo FJ); Fang Peifen (Fang Pf) and Li Yuanchao (Li YC)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     Messaoenolide
C30H48O4     ÏàËÆ¶È:63.3%
Phytochemistry          1996          41          1573-1577
Triterpenoids from Melilotus messanensis; soyasapogenol G, the first natural carbonate derivative
Francisco A. Mac¨ªas*, Ana M. Simonet, M. Dolores Esteban, Juan Carlos G. Galindo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     Neoalsooenin A
    ÏàËÆ¶È:63.3%
Phytochemistry          1995          38          465-472
Dammarane glycosides from aerial parts of Neoalsomitra integrifoliola
Seiji Fujita, Ryoji Kasai, Kazuhiro Ohtani, Kazuo Yamasaki, Ming-Hua Chiu, Rui-Lin Nie, Osamu Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     20(S)-protopanaxadiol oxide I
    ÏàËÆ¶È:63.3%
Phytochemistry          1995          38          465-472
Dammarane glycosides from aerial parts of Neoalsomitra integrifoliola
Seiji Fujita, Ryoji Kasai, Kazuhiro Ohtani, Kazuo Yamasaki, Ming-Hua Chiu, Rui-Lin Nie, Osamu Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     Neoalsogenin G
C30H50O4     ÏàËÆ¶È:63.3%
Phytochemistry          1995          38          465-472
Dammarane glycosides from aerial parts of Neoalsomitra integrifoliola
Seiji Fujita, Ryoji Kasai, Kazuhiro Ohtani, Kazuo Yamasaki, Ming-Hua Chiu, Rui-Lin Nie, Osamu Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     yunganogcnin F
    ÏàËÆ¶È:63.3%
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
25 .     pomolic acid
    ÏàËÆ¶È:63.3%
Phytochemistry          1992          31          1317-1320
Pomolic acid derivatives from the rootof Sanguisorba officinalis
Cheng, D. and Cao, X.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     yunganogenin F
C30H46O5     ÏàËÆ¶È:63.3%
Phytochemistry          1992          31          1747-1752
Oleanane glycosides from Glycyrrhiza yunnanensis roots
Kazuhiro Ohtani, Katsuki Ogawa, Ryoji Kasai, Chong-Ren Yang, Kazuo Yamasaki, Jun Zhou, Osamu Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     neoalsogenin A
C30H52O5     ÏàËÆ¶È:63.3%
Phytochemistry          1992          31          2451-2453
A dammarane saponin from Neoalsomitra integrifoliola
Hiromichi Nagasawa, Akira Isogai, Akinori Suzuki, Chiu Minghua, Nie Ruilin, Zhou Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     (23R)-and (23S)-21,23-Epoxy-5¦Á-cycloart-24-en-3¦Â-ol
C30H48O2     ÏàËÆ¶È:63.3%
Phytochemistry          1992          31          4263-4274
Cycloartanes and other terpenoids and phenylpropanoids from Monocyclanthus vignei
Hans Achenbach, Dieter Frey
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     compound 12
    ÏàËÆ¶È:63.3%
Phytochemistry          1992          31          4263-4274
Cycloartanes and other terpenoids and phenylpropanoids from Monocyclanthus vignei
Hans Achenbach, Dieter Frey
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     Compound 10
    ÏàËÆ¶È:63.3%
Phytochemical Analysis          2009          20          320-327
Antioxidant diterpenoids from the roots of Salvia barrelieri
Ufuk Kolak, Ahmed Kabouche, Mehmet Özt¨¹rk, Zahia Kabouche, G¨¹laçtl Topçu and Ayhan Ulubelen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     Compound 1a
    ÏàËÆ¶È:63.3%
Phytochemical Analysis          2009          20          320-327
Antioxidant diterpenoids from the roots of Salvia barrelieri
Ufuk Kolak, Ahmed Kabouche, Mehmet Özt¨¹rk, Zahia Kabouche, G¨¹laçtl Topçu and Ayhan Ulubelen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     maytenfolic acid
C30H48O4     ÏàËÆ¶È:63.3%
Phytochemistry          1986          25          479-485
Antitumour triterpenes of Maytenus diversifolia
Hiroshi Nozaki, Hideyo Suzuki, Teruhisa Hirayama, Ryoji Kasai, Rong-Yang Wu, Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     ¦Á-amyrin
    ÏàËÆ¶È:63.3%
Chinese Traditional and Herbal Drugs          2008          39          1296-1298
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ÖÜÔ¨;¼½±£È«;Íõì¿;ãÆÐ˹ú;Ê·ÀöÓ±;ÍõÓÀÆæ;·ë±¦Ãñ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     ÐܹûËá
    ÏàËÆ¶È:63.3%
Chinese Traditional and Herbal Drugs          2008          39          499-502
¿ÕÐÄÁ«×Ӳݻ¯Ñ§³É·ÖÑо¿
Âí׿;ÀîÇíÛë;·¶ÎÄǬ;·½Äî²®;ÁõìÍÎÄ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     ursolic acid
    ÏàËÆ¶È:63.3%
Chinese Traditional and Herbal Drugs          1995          26          339-341+391
Studies on the Chemical Constituents of Indian Mockstrawberry(Duchesnea indica)
Peng Jiangnan; Lu Yunru and Chen Dechang(Department of Materia Madica; Beijing college of Traditional Chinese; Beijing);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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