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1 .     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
2 .     ursolic acid
    ÏàËÆ¶È:66.6%
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
3 .     euscaphic acid
    ÏàËÆ¶È:66.6%
Pharmazie          2008          63          765-767
Euscaphic acid, a new hypoglycemic natural product from Folium Eriobotryae
Jian Chen, Wei-Lin Li, Ju-Lan Wu, Bing-Ru Ren and Han-Qing Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     euscaphic acid
    ÏàËÆ¶È:66.6%
Chinese Pharmaceutical Journal          2005          40          1052-1054
Study on chemical constituents of Potentilla discolor
XLE Pei-feng, YIN Ting, LIANG Hong, ZHAO Yu-ying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     euscaphic acid
    ÏàËÆ¶È:66.6%
Journal of Peking University (Health Sciences)          2004          36          21-23
Studies on the chemical constituents from Potentilla multifida L.
XUE Pei feng; QIAO Liang; LIANG Hong; ZHAO Yu ying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     2¦Á,3¦Á,19¦Á-ÈýôÇ»ù-12 Ï©-28-ÎÚËÕËá
    ÏàËÆ¶È:66.6%
Chinese Traditional and Herbal Drugs          2011          42          2200-2203
Chemical constituents in Potentilla kleiniana
LI, Sheng-hua, WU, Xian-jin, NIU, You-ya, ZENG, Jun-ying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Larreagenin A
    ÏàËÆ¶È:65.5%
Planta Medica          1989          55          303-306
Yemuoside YM7, YM11, YM13, and YM14:Four Nortriterpenoid Saponins from Stauntonia chinensis
Huai-Bin Wang,De-Quan Yu,Xiao-Tian Liang, Naoharu Watanabe, Masaharu Tamai, and Sadafumi Omura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     30-nor,larreagenin A
    ÏàËÆ¶È:65.5%
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
9 .     (22R)-methylcholest-5-en-3¦Â,22,28-tetraol-3,22,28-triacetate
    ÏàËÆ¶È:65.5%
Chinese Journal of Chemistry          2001          19          515-517
Sardisterol, A New Polyhydroxylated Sterol from the Soft Coral Sarcophyton digitatum Moser
Jing-Yu Su, Ruo-Lin Yang and Long-Mei Zeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     methyl pomolate
    ÏàËÆ¶È:64.5%
Chemical & Pharmaceutical Bulletin          1987          35          841-845
Two New Triterpenoid Glycosides from Leaves of Ilex chinensis SIMS
AKIRA INADA,MARI KOBAYASHI,HIROKO MURATA and TSUTOMU NAKANISHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     ilexpernoside J
C48H78O20     ÏàËÆ¶È:63.3%
Helvetica Chimica Acta          2008          Vol. 91          1630
Triterpene Saponins from the Leaves of Ilex pernyi
Guang-Bo Xie, Jiao Zheng, Peng-Fei Tu, and Guo-Qing Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     3¦Â-hydroxy-12-oxo-13H¦Á-olean-28,19¦Â-olide
C30H46O4     ÏàËÆ¶È:63.3%
Journal of Natural Products          2006          69(5)          807-810
Triterpenoids from the Resin of Styrax tonkinensis and Their Antiproliferative and Differentiation Effects in Human Leukemia HL-60 Cells
Feng Wang, Huiming Hua, Yuehu Pei, Duo Chen, and Yongkui Jing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     compound 9
    ÏàËÆ¶È:63.3%
Journal of Natural Products          1996          59          304-307
Triterpenoids from Adina rubella
Shi-yue Fang, Zhi-sheng He, and Gao-jun Fan, Hou-ming Wu and Jing-fei Xu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     pomolic acid
C36H46O4     ÏàËÆ¶È:63.3%
Chemical & Pharmaceutical Bulletin          1992          40          1990-1992
Triterpenoid Saponins of Aquifoliaceous Plants. V. Ilexosides XV-XIX from the Barks of Ilex crenata THUNB.
Chieko HATA,Miho KAKUNO,Kazuko YOSHIKAWA and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     pomolic acid
C30H48O4     ÏàËÆ¶È:63.3%
Chemical & Pharmaceutical Bulletin          1992          40          3138-3141
Triterpenoid Saponins of Aquifoliaceous Plants. VIII. Ilexosides XXIX-XXXII from the Leaves of Ilex rotunda THUNB.
Kayoko AMIMOTO,Kazuko YOSHIKAWA and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     20(S),24(R)-epoxydammarane-3¦Â,11¦Â,25-triol
    ÏàËÆ¶È:63.3%
Chemistry of Natural Compounds          1980          16          40-43
REFINEMENT OF THE STBUCTUBES OF TBITEB PENES FEOM THE LEAVES OF Betula ermanii
V. L. Novikov, G. V, Malino vskaya, N. D. Pokhilo, and N. I. Uvarova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     3¦Â,19-dihydroxyolean-12-en-28-oic acid
C30H48O4     ÏàËÆ¶È:63.3%
Acta Botanica Boreali-Occidentalia Sinica          2007          27          1141-1146
The Triterpenes in Salvia umbratica
LIU Qing, LIU Zhen-ling, TIAN Xuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     glyyunnansapogenin B2
    ÏàËÆ¶È:63.3%
Acta Pharmaceutica Sinica          1995          30          27-33
NEW TRTEKPENOIDAL SAPOGENINS FROM THE ROOTS OF GLYCYRRHIZA YUNNANENSIS
JF Hu; ZL Ye and FJ Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     compound S
    ÏàËÆ¶È:63.3%
Journal of Asian Natural Products Research          2005          7          829-834
Two new triterpenoid saponins from Sarcandra glab
Y.-M. LUO, A.-H. LIU, D.-M. ZHANG and L.-Q. HUANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     2¦Á,3¦Á,19¦Á,23-Tetrahydroxyurs-12-en-28-oic Acid
    ÏàËÆ¶È:63.3%
Journal of Asian Natural Products Research          2003          5          49-56
BIOACTIVE TRITERPENOIDS FROM SYMPLOCOS CHINENSIS
XI-HAO LI, DIAN-DIAN SHEN, NAN LI and SHI-SHAN YU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     euscaphic acid
    ÏàËÆ¶È:63.3%
Natural Product Research          2008          22          1310-1316
Two new 11¦Á,12¦Á-epoxy-ursan-28,13¦Â-olides and other triterpenes from Cecropia catharinensis
E. C. Machado; R. A. Yunes; A. Malheiros; E. C. Gomez; F. Delle Monache
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     pomolic acid
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2005          30          1833-1836
Triterpenes from root of Rhaponticum uniflorum
ZHANG Yonghong, ZHANG Jiangang, XIE Jieming, CHEN Gelin, CHENG Dongliang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     Euscaphic acid
C30H48O5     ÏàËÆ¶È:63.3%
Journal of Natural Products          1989          Vol 52          162
Pentacyclic Triterpenes from the Fruits of Rosa sterilis
Liang Guang-Yi, Alexander I. Gray, Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     alamosenogenin
C30H48O4     ÏàËÆ¶È:63.3%
Journal of Natural Products          1995          Vol 58          1913-1914
A New Triterpene from Rathbunia alamosensis
Takaomi Takizawa, Kaoru Kinoshita, Kiyotaka Koyama, Kunio Takahashi, Norio Kondo, Hiroshi Yuasa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     compound 34
    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
26 .     pomolic acid
    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
27 .     compound 232
    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
28 .     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
29 .     pomolic acid
C30H48O4     ÏàËÆ¶È:63.3%
Phytochemistry          1992          31          2809-2812
Triterpene saponins from fruit of Ilex crenata
Takashi Kakuno, Kazuko Yoshikawa, Shigenobu Arihara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     pomolic acid
C30H46O4     ÏàËÆ¶È:63.3%
Phytochemistry          1992          31          3553-3557
Saturated hopane and gammacerane triterpene-diols from the stem bark of Abies veitchii
Reiko Tanaka, Shunyo Matsunaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     euscaphic acid
    ÏàËÆ¶È:63.3%
Journal of Natural Products          2010          73          1655-1658
Cytotoxic Hexacyclic Triterpene Acids from Euscaphis japonica
Jing-Jy Cheng, Li-Jie Zhang, Hui-Ling Cheng, Chun-Tang Chiou, I-Jung Lee, and Yao-Haur Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     rotungenic acid
C30H48O5     ÏàËÆ¶È:63.3%
Phytochemistry          1989          28          1479-1482
Triterpenes from Ilex rotunda fruits
Munehiro Nakatani,Yuji Miyazaki,Takashi Iwashita,Hideo Naoki,Tsunao Hase
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     3¦Â,22¦Â-dihydroxy-olean-12-en-29-oic acid (22-epi-maytenfolic acid)
C30H48O4     ÏàËÆ¶È:63.3%
Magnetic Resonance in Chemistry          2002          40          366-370
Epikatonic acid from Austroplenckia populnea: structure elucidation by 2D NMR spectroscopy and X-ray crystallography
G. D. F. Silva, L. P. Duarte, S. A. Vieira Filho, A. C. Doriguetto, Y. P. Mascarenhas, J. Ellena, E. E. Castellano and A. B. Cota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     19¦Á-ôÇ»ùÎÚËÕËá
    ÏàËÆ¶È:63.3%
Chinese Traditional and Herbal Drugs          2009          40          369-371
×϶¡ÏãÒ¶»¯Ñ§³É·ÖÑо¿
ÀîÈ«;ÐíÇíÃ÷;ºÂÀöÀò;½±ù·Ò;ÑîÊÀÁÖ;ÀîЦȻ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     rotungenic acid
C30H46O5     ÏàËÆ¶È:63.3%
Chinese Traditional and Herbal Drugs          2009          40          1036-1039
ŵÀöÇà¹û»¯Ñ§³É·ÖÑо¿
ÌÀ½¨¹ú;Èθ£²Å;Áõ¼ª¿ª
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     pomolic acid
    ÏàËÆ¶È:63.3%
Chinese Traditional and Herbal Drugs          2006          37          1632-1633
èÁèËÒ¶µÄ»¯Ñ§³É·ÖÑо¿(¢ñ)
³Â½£;ÀîάÁÖ;Îâ¾ÕÀ¼;Õź­Çì
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     6¦Â,19¦Á-dihydroxy ursolic acid
C30H48O5     ÏàËÆ¶È:63.3%
Chinese Journal of Natural Medicines          2007          5          413-416
Chemical Constituents from Hypericum ascyron
GAO Ying; HAN Li; SUN Liang; ZHENG Dan; HUANG Xue-Shi; YU Shi-Shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     euscaphic acid
C30H48O5     ÏàËÆ¶È:63.3%
Chinese Journal of Natural Medicines          2010          8          12-15
Triterpenoids from the Roots of Rose odorata var.gigantean
LIU Dai-Lin; ZHU Shan; MA Rong; ZHANG Jing-Ze; LI He-Yu; CHEN Hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     euscaphic acid
    ÏàËÆ¶È:63.3%
Journal of China Pharmaceutical University          2002          33          184-187
Studies on the Constituents of Rosa multiflora Thunb
LI Yan Fang*; HU Li Hong; LOU Feng Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     pomolic acid
C30H48O4     ÏàËÆ¶È:63.3%
Natural Product Research and Development          2001          13(2)          11-13
THE STUDIES OF CHEMICAL COMPONENTS OF CLAUSENA DUNNIANA
CUI Shu ya;CHENG Dong liang; TIAN Jun; WU Feng e
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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