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»¯ºÏÎï14£º13C NMR (101 MHz, CDCl3) ¦Ä 215.85, 144.62, 124.16, 82.73, 79.17, 66.46, 52.11, 47.90, 45.52, 44.44, 43.00, 40.00, 38.59, 36.10, 34.12, 29.62, 29.53, 28.79, 28.01, 27.44, 25.76, 25.15, 25.09, 18.15, 16.73, 16.01.

»¯ºÏÎï15£º13C NMR (151 MHz, MeOD) ¦Ä 139.87, 126.69, 79.69, 56.74, 54.48, 43.28, 40.77, 40.55, 40.47, 39.99, 39.86, 38.28, 38.11, 34.38, 31.91, 29.28, 28.79, 27.89, 25.44, 24.38, 24.09, 21.67, 19.50, 17.95, 17.73, 16.43, 16.06.

»¯ºÏÎï17£º13C NMR (151 MHz, MeOD) ¦Ä 184.68, 178.37, 139.87, 129.28, 73.98, 73.85, 68.90, 66.67, 55.52, 44.20, 43.13, 43.11, 41.69, 41.56, 40.11, 39.39, 37.37, 29.78, 27.59, 27.23, 26.92, 24.90, 24.66, 18.76, 17.68, 16.75, 14.16.
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458699070: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-12-05 10:41:30
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1 .     2¦Á,3¦Á,19¦Á,23-tetrahydroxyolean-12-en-28-oic acid
C30H48O6     ÏàËƶÈ:70%
Journal of Natural Products          2011          74          732-738
Anti-inflammatory Triterpenes from the Leaves of Rosa laevigata
Na Zeng, Yang Shen, Ling-Zhi Li, Wei-Hua Jiao, Pin-Yi Gao, Shao-Jiang Song, Wan-Sheng Chen, and Hou-Wen Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     methyl 3¦Â,19¦Â-dihydroxyolean-12-en-28-oate
    ÏàËƶÈ:67.7%
Korean Journal of Pharmacognosy          1987          18(3)          151-167
13C NMR Spectroscopy of Amyrins
Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     11Ò»ÍÑÑõ¸Ê²Ý´ÎËá
    ÏàËƶÈ:65.5%
Chinese Traditional and Herbal Drugs          2006          37          20-25
Novel 11-deoxylglycyrrhetinic acid-30-acylamide derivatives
TANG Li-da; WANG Jian-wu; YONG Jian-ping; ZHANG Shi-jun; LIU Li-jun; WANG Yu-li; WU Nan; XU Wei-ren
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     Wilforlide A
    ÏàËƶÈ:65.5%
Chinese Pharmaceutical Journal          2009          44          1375-1377
Studies on Chemical Constituents of the Euonymus alatus(Thunb.) Sieb.¢ò
ZHOU Xin, LIU Yun, GONG Xiao-jian, ZHAO Chao, CHEN Hua-guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     Neriagenin
    ÏàËƶÈ:65.3%
Chemical & Pharmaceutical Bulletin          2011          59(3)          371-377
The Structure of a New Cardenolide Diglycoside and the Biological Activities of Eleven Cardenolide Diglycosides from Nerium oleander
Ming ZHAO,Liming BAI, Asami TOKI, Ryo HASEGAWA, Jun-ichi SAKAI, Toshiaki HASEGAWA, Hirotsugu OGURA, Takao KATAOKA, Yuhua BAI, Mariko ANDO, Katsutoshi HIROSE,and Masayoshi ANDO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     4-Nor-3-oxo-4-oxa-5¦Á-Cholestane
C26H44O2     ÏàËƶÈ:65.3%
Steroids          2011          76          1341-1345
Expedited Baeyer¨CVilliger oxidation of steroidal ketones by microwave irradiation
Juri Moni Borah, Pritish Chowdhury
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     A-nor-3-Oxo-5¦ÂH-olean-12-en-30-oic Acid
    ÏàËƶÈ:64.2%
Chemistry of Natural Compounds          2006          42          553-557
SYNTHESIS AND HIGH-RESOLUTION NMR SPECTRA OF A-nor-DERIVATIVES OF 11-DEOXYGLYCYRRHETIC ACID
L. R. Mikhailova, L. A. Baltina, R. M. Kondratenko,. Kunert,L. V. Spirikhin,F. Z. Galin, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     ganoderic acid ¦Å
C30H44O7     ÏàËƶÈ:63.3%
Chemical & Pharmaceutical Bulletin          2000          48(7)          1026-1033
Triterpenes from the Spores of Ganoderma lucidum and Their Cytotoxicity against Meth-A and LLC Tumor Cells
Byung-Sun MIN,Jiang-Jing GAO,Norio NAKAMURA and Masao HATTORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     3¦Â-hydroxylanosta-8,24-dien-21-oic acid
C30H48O3     ÏàËƶÈ:63.3%
Journal of Natural Products          1998          61          193-197
Fomitellic Acids, Triterpenoid Inhibitors of Eukaryotic DNA Polymerases from a Basidiomycete, Fomitella fraxinea
Nobukazu Tanaka, Akitoshi Kitamura, Yoshiyuki Mizushina, Fumio Sugawara, and Kengo Sakaguchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     dihydroochraceolide A
C30H46O3     ÏàËƶÈ:63.3%
Journal of Natural Products          1996          59          658-663
Lupane Derivatives from Lophopetalum wallichii with Farnesyl Protein Transferase Inhibitory Activity
Sonja Sturm, Roberto R. Gil, Hee-Byung Chai, Olipa D. Ngassapa, Thawatchai Santisuk, Vichai Reutrakul, Anne Howe, Marcia Moss, Jeffrey M. Besterman, Shi-Lin Yang, John E. Farthing, R. Murray Tait, Jane A. Lewis, Melanie J. O¡¯Neill, Norman R. Farnsworth, G
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     11-deoxyglycyrrhetinic acid
    ÏàËƶÈ:63.3%
Chemistry of Natural Compounds          2008          44          194-196
SYNTHESIS OF GLYCYRRHETIC ACID DERIVATIVES
J.-P. Yong, J.-W. Wang, H. A. Aisa, and L.-J. Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     julibrotriterpenoidal lacrone A
    ÏàËƶÈ:63.3%
Acta Pharmaceutica Sinica          1997          32          144-147
STUDIES ON THE TRITERPENE SAPOGENINS FROM ALBIZZIAE CORTEX
SP Chen and RY Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     ganoderic acid ¦Å
C30H44O7     ÏàËƶÈ:63.3%
Journal of Asian Natural Products Research          2002          4          129-134
A NEW LANOSTANE-TYPE TRITERPENE FROM THE FRUITING BODIES OF GANODERMA LUCIDUM
JUN LUO, YU-YING ZHAO and ZHI-BIN LIN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

14 .     Protosta-20,24-dien-3¦Â-ol
    ÏàËƶÈ:63.3%
Phytochemistry          2012          76          83-91
Diterpenoids and triterpenoids with potential anti-inflammatory activity from the leaves of Aglaia odorata
Orapun Yodsaoue,Jarinthon Sonprasit,Chatchanok Karalai,Chanita Ponglimanont,Supinya Tewtrakul,Suchada Chantrapromma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     oleanic acid
    ÏàËƶÈ:63.3%
Chinese Pharmaceutical Journal          2006          41          1452-1454
Studies on Chemical Constituents of Mangrove Plant Scyphiphora hydrophyllacea
DAI Hao-fu, MEI Wen-li*, WU Jiao, LI Xiao-ming, WANG Bin-gui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     3¦Â-hydroxytirucallic acid
C30H48O3     ÏàËƶÈ:63.3%
Zeitschrift f¨¹r Naturforschung C          2003          58          505-516
Immunomodulatory Triterpenoids from the Oleogum Resin of Boswellia carterii Birdwood
F. A. Badria, B. R. Mikhaeil, G. T. Maatooq, and M. M. A. Amer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     protosta-20,24-dien-3¦Â-ol
    ÏàËƶÈ:63.3%
Journal of the American Chemical Society          2006          128          6414-6419
Site-Saturated Mutagenesis of Histidine 234 of Saccharomyces cerevisiae Oxidosqualene-Lanosterol Cyclase Demonstrates Dual Functions in Cyclization and Rearrangement Reactions
Tung-Kung Wu, Yuan-Ting Liu, Cheng-Hsiang Chang, Mei-Ting Yu, and Hisng-Ju Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     lucidenic acid SP1
C27H40O6     ÏàËƶÈ:62.9%
Planta Medica          2001          67          811-814
Anticomplement Activity of Terpenoids from the Spores of Ganoderma lucidum
Byung Sun Min,Jiang Jing Gao,Masao Hattori,Hyeong Kyu Lee,Young Ho Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

19 .     3¦Á,22¦Â-dihydroxyolean-12-ene
C30H50O2     ÏàËƶÈ:62.0%
Natural Product Research          2002          16          415-418
Alysinol - A New Triterpene from Alysicarpus Monolifer
Naheed Riaz; Itrat Anis; Pir Muhammad Khan; Raza Shah; Abdul Malik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

20 .     aphidicolin bisacetonide
    ÏàËƶÈ:61.5%
Phytochemistry          1992          31          799-803
Aphidicolane metabolites of Cephalosporium aphidicola
James R. Hanson, Peter B. Hitchcock, Andrew G. Jarvis, Elsa M. Rodriguez-Perez, Arnold H. Ratcliffe
2Â¥2012-12-03 14:45:03
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458699070: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-12-04 11:01:04
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1 .     ursolic acid
    ÏàËƶÈ:92.8%
Phytochemistry          1992          31          3909-3914
Triterpenoids from plants of the sanguisorbeae
Gesa Reher, Miloš Bud¨§š¨ªnský
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     ursolic acid
    ÏàËƶÈ:92.5%
Food Chemistry          2011          124          468-475
Analysis of the anti-inflammatory properties of Rosmarinus officinalis L. in mice
Juc¨¦lia Pizzetti Beninc¨¢, Juliana Bastos Dalmarco, Moacir Geraldo Pizzolatti, Tânia Silvia Fröde
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     ÎÚËÕËá
    ÏàËƶÈ:90%
Chinese Traditional and Herbal Drugs          2008          39          978-981
ÈÕ±¾Â·±ßÇàµÄ»¯Ñ§³É·ÖÑо¿
ÕÔ¾§;¸ßÎÄÔ¶;¶ÎºêȪ;ëø½Ü;¸ßʯϲ¾Ã
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     ursolic acid
    ÏàËƶÈ:90%
Tropical Journal of Pharmaceutical Research          2010          9          135-140
Anti-leishmanial and Anti-cancer Activities of a Pentacyclic Triterpenoid Isolated from the Leaves of Terminalia arjuna Combretaceae
Biswas Moulisha*, Ghosh Ashok Kumar, Haldar Pallab Kanti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     ursolic acid
    ÏàËƶÈ:90%
Food Chemistry          2006          98          285-290
Annurcoic acid: A new antioxidant ursane triterpene from fruits of cv. Annurca apple
Brigida D¡¯Abrosca, Antonio Fiorentino, Pietro Monaco, Palma Oriano, Severina Pacifico
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     ¦Á-Amyrin
    ÏàËƶÈ:89.6%
Archives of Pharmacal Research          2008          31          823-829
Chemical constituents of Acanthus ilicifolius L. and effect on osteoblastic MC3T3E1 cells
Phan Van Kiem, Tran Hong Quang, Tran Thu Huong, Le Thi Hong Nhung and Nguyen Xuan Cuong, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     ÎÚËÕËá
    ÏàËƶÈ:86.6%
Chinese Traditional and Herbal Drugs          2010          41          370-373
½ðÁ«»¨µÄ»¯Ñ§³É·ÖÑо¿
ÁõÕÙÑô;ÂÞ¶¼Ç¿
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     ursolic acid
    ÏàËƶÈ:86.6%
Chinese Pharmaceutical Journal          2006          41          1452-1454
Studies on Chemical Constituents of Mangrove Plant Scyphiphora hydrophyllacea
DAI Hao-fu, MEI Wen-li*, WU Jiao, LI Xiao-ming, WANG Bin-gui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     ursolic acid
    ÏàËƶÈ:86.6%
Journal of Shenyang Pharmaceutical University          2007          24          549-551
Isolation and identification of non-alkaloid constituents from Gelsemium elegans Benth.
ZHAO Qing-chun, FU Yan-hui, GU O Tao, HU A Wei, WU Li-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     Ursolic acid
    ÏàËƶÈ:86.6%
Chinese Journal of Pesticide Science          2009          11          235-238
Inhibitory Effects of Three Compounds Extracted from Trollius ledebouri on Phenoloxidase of Spodotera exigua
YANG Fan; ; LIU Zhao-yang; LIU Wei; DU Lei; XUE Chao-bin; LUO Wan-chun
3Â¥2012-12-03 14:48:56
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458699070: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-12-04 11:18:05
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1 .     2¦Á,3¦Â,19¦Á,23¦Â-tetrahydroxyurs-12-en-28-oic acid
    ÏàËƶÈ:76.6%
China Journal of Chinese Materia Medica          2009          34          3047-3050
Triterpenoid constituents in fruits of Psidum guajava
SHU Jicheng, CHOU Guixin, WANG Zhengtao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     3¦Â,19¦Á,23¦Â-trihydroxylurs-12-en-28-oic acid
    ÏàËƶÈ:73.3%
China Journal of Chinese Materia Medica          2009          34          3047-3050
Triterpenoid constituents in fruits of Psidum guajava
SHU Jicheng, CHOU Guixin, WANG Zhengtao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     3,23-disulfate ester of 23-hydroxytormentic acid
C30H48O12S2     ÏàËƶÈ:70%
Journal of Natural Products          2007          70          1889-1894
Triterpene, Antioxidant, and Antimicrobial Compounds from Melissa officinalis
Teresa Mencherini,Patrizia Picerno, Carla Scesa, and Rita Aquino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     euscaphic acid
C30H48O5     ÏàËƶÈ:70%
China Journal of Chinese Materia Medica          2006          31          1875-1879
Triterpenes from herb of Potentilla chinesis
LIU Pu, DUAN Hongquan, PAN Qin, ZHANG Yanwen, YAO Zhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     myrianthic acid
C30H48O6     ÏàËƶÈ:70%
China Journal of Chinese Materia Medica          2006          31          1875-1879
Triterpenes from herb of Potentilla chinesis
LIU Pu, DUAN Hongquan, PAN Qin, ZHANG Yanwen, YAO Zhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     6¦Â,23-dihydroxy-tormentic acid
C30H48O7     ÏàËƶÈ:70%
Phytochemistry          1993          34          497-499
A saponin from leaves of Aphloia madagascariensis
Marie-Genevi¨¨ve Dijoux, Catherine Lavaud, Georges Massiot, Louisette Le Men-Olivier, Douglas M. Sheeley
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     compound Ia
    ÏàËƶÈ:70%
Korean Journal of Pharmacognosy          1987          18(3)          188-190
A Triterpene Glycoside in Berries of Rubus coreanus
Kim, Eun; Kim, Young-Choong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     euscaphic acid
    ÏàËƶÈ:70%
Chinese Traditional and Herbal Drugs          2007          38          1311-1313
ÉßÝ®ÖоßÓп¹°©»îÐÔµÄÈýÝÆÀà³É·Ö
ÎâÅàéª;¶ÎºêȪ;Ò¦ÖÇ;ÅËÇÚ;ÕŸ»âÙ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     2¦Á,3¦Á,19¦Á,23-tetrahydroxyurs-12-en-28-oic acid
C30H48O6     ÏàËƶÈ:70%
Chinese Journal of Natural Medicines          2006          4          271-274
Isolation and Identification of Terpenes from Coleus forskohlii
SHAN Yu-Pei; KONG Ling-Yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     2¦Á,3¦Â,19¦Á-Trihydroxy-28-norurs-12-ene
C29H48O3     ÏàËƶÈ:68.9%
Chemical & Pharmaceutical Bulletin          2005          53(10)          1338-1341
Sesquiterpenes, Nortriterpenes and Other Constituents from Ligularia tongolensis
Yi Feng HAN,Jing PAN,Kun GAO,and Zhong Jian JIA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     2¦Á,3¦Á,19¦Á-Trihydroxy-28-norurs-12-ene
C29H48O3     ÏàËƶÈ:68.9%
Chemical & Pharmaceutical Bulletin          2005          53(10)          1338-1341
Sesquiterpenes, Nortriterpenes and Other Constituents from Ligularia tongolensis
Yi Feng HAN,Jing PAN,Kun GAO,and Zhong Jian JIA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     2¦Á,3¦Â,19¦Á-trihydroxy-28-norurs-12-ene
C29H48O3     ÏàËƶÈ:68.9%
Chemistry Letters          2005          34          892-893
Two New Nortriterpenes from Ligularia tongolensis
Yi Feng Han, Kun Gao and Zhong Jian Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     2¦Á,3¦Á,19¦Á-trihydroxy-28-norurs-12-ene
C29H47O2     ÏàËƶÈ:68.9%
Chemistry Letters          2005          34          892-893
Two New Nortriterpenes from Ligularia tongolensis
Yi Feng Han, Kun Gao and Zhong Jian Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

14 .     3¦Â,19¦Á-Dihydroxy-6-oxo-urs-12-en-23-ol-28-oic acid
C30H44O6     ÏàËƶÈ:68.9%
Tetrahedron          2000          56          547-552
Two New 19-Hydroxyursolic Acid-type Triterpenes from Peruvian ¡®Uña de Gato¡¯ (Uncaria tomentosa)
Mariko Kitajima, Ken-ichiro Hashimoto, Masashi Yokoya, Hiromitsu Takayama, Norio Aimi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     19-O-substitutedurs-1 2-en-28-oic acid deriative
C30H48O5     ÏàËƶÈ:66.6%
Planta Medica          1990          56          330-332
Polyhydroxylated Triterpenes from Eriobotryajaponica
Zhou Zhong Liang , Rita Aquino, Vincenzo De Feo,Francesco De Szmone, and Cosimo Pizza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     pomolic acid
C30H48O4     ÏàËƶÈ:66.6%
China Journal of Chinese Materia Medica          2006          31          1875-1879
Triterpenes from herb of Potentilla chinesis
LIU Pu, DUAN Hongquan, PAN Qin, ZHANG Yanwen, YAO Zhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     2¦Â,3¦Â,19¦Á-trihydroxyurs-12-en-28-oic acid
C30H48O5     ÏàËƶÈ:66.6%
China Journal of Chinese Materia Medica          2006          31          1875-1879
Triterpenes from herb of Potentilla chinesis
LIU Pu, DUAN Hongquan, PAN Qin, ZHANG Yanwen, YAO Zhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     compound 226
    ÏàËƶÈ:66.6%
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
--------------------------------------------------------------------------------

19 .     euscaphic acid
    ÏàËƶÈ:66.6%
Chinese Traditional and Herbal Drugs          2002          33          99-101
Triterpenes from Rubus parkeri root
TAO Zheng ming; DING Li sheng; Peng Shu lin; WANG Ming kui; ZHANG An jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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20 .     tormentic acid
    ÏàËƶÈ:65.5%
Phytochemistry          1992          31          3909-3914
Triterpenoids from plants of the sanguisorbeae
Gesa Reher, Miloš Bud¨§š¨ªnský
4Â¥2012-12-03 14:52:16
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