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1 .     compound Ia
    ÏàËÆ¶È:83.3%
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

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2 .     2¦Á,3¦Á,19¦Á,23-tetraydroxy-urs-12-en-28-oic acid
    ÏàËÆ¶È:82.7%
Chinese Traditional and Herbal Drugs          2012          43          1285-1288
Study on chemical constituents from Potentilla supina
ZHENG Guang-hai; PIAO Hui-shun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     2¦Â,3¦Â,19¦Á-trihydroxyurs-12-en-28-oic acid
C30H48O5     ÏàËÆ¶È:80%
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

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4 .     myrianthic acid
C30H48O6     ÏàËÆ¶È:80%
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

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5 .     2¦Á,3¦Á,19¦Á,23-tetrahydroxyurs-12-en-28-oic acid
C30H48O6     ÏàËÆ¶È:80%
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

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6 .     tormentic acid
    ÏàËÆ¶È:79.3%
Phytochemistry          1992          31          3909-3914
Triterpenoids from plants of the sanguisorbeae
Gesa Reher, Miloš Bud¨§š¨ªnský
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     19¦Á-Hydroxyasiatic acid
C30H50O4     ÏàËÆ¶È:79.3%
Natural Product Research and Development          2012          24          757-760
Chemical Constituents from Stems of Rhododendron delavayi Franch.
XU Jin-jin; WANG Yue-hu; WANG Hong-sheng; WANG Huan; HUANG Qiao-qin; LONG Chun-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     2-epi-tormentic acid
C30H48O5     ÏàËÆ¶È:76.6%
Phytochemistry          2009          70          1239-1245
Hydroperoxy-cycloartane triterpenoids from the leaves of Markhamia lutea,a plant ingested by wild chimpanzees
Damien Lacroix, Soizic Prado, Alexandre Deville, Sabrina Krief, Vincent Dumontet, John Kasenene, Elisabeth Mouray, Christian Bories, Bernard Bodo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     compound 3
    ÏàËÆ¶È:76.6%
Phytochemistry          1988          27          3975-3976
A triterpene from the fruits of Rubus chingii
Masao Hattori,kue-Ping Kuo,Yue-Zhong Shu,Yasuhiro Tezuka,Tohru Kikuchi,Tsuneo Namba
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     3¦Â-trans-ferulyl-2¦Á,19¦Á-dihydroxy-urs-12-en-28-oic acid
C40H45O8     ÏàËÆ¶È:76.6%
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

--------------------------------------------------------------------------------

11 .     23-hydroxytormentic acid 28-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:76.6%
Natural Product Research and Development          2001          13(1)          21-23
THE CHEMICAL CONSTITUTE FROM ROSA LAEVIGATA MICHX
WANG Jin yi;ZHANG Guo lin; CHENG Dong ling; WU Fen e
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

12 .     2¦Á,3¦Á,19-trihydroxyurs-12-en-28-oic acid
    ÏàËÆ¶È:76.6%
Shoyakugaku Zasshi          1992          46          202-205
Pentacyclic Triterpenes from Salvia paramiltiorrhiza
SUN XIAO-RU, LUO HOU-WEI, SAKAI TATSUKO, NIWA MASATAKE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     tormentic acid
    ÏàËÆ¶È:76.6%
Chinese Traditional and Herbal Drugs          2012          43          851-855
Chemical constituents of Agrimoniae Herba
LU Fang; BA Xiao-yu; HE Yong-zhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     2¦Á,3¦Â,19¦Á-Trihydroxy-28-norurs-12-ene
C29H48O3     ÏàËÆ¶È:75.8%
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

--------------------------------------------------------------------------------

15 .     2¦Á,3¦Â,19¦Á-trihydroxy-28-norurs-12-ene
C29H48O3     ÏàËÆ¶È:75.8%
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

--------------------------------------------------------------------------------

16 .     tormentic acid
    ÏàËÆ¶È:75.8%
Korean Journal of Pharmacognosy          2011          42          223-228
Phytochemical Constituents Isolated from the Stems of Chaenomeles sinensis Koehne
Shin, Ji-Eun; Jin, Qing-Long; Jin, Hong-Guang; Woo, Eun-Rhan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     ¨¢cido torm¨ºntico
    ÏàËÆ¶È:75.8%
Qu¨ªmica Nova          2008          31          744-750
Chemical constituents and antiedematogenic activity of Peltodon radicans (Lamiaceae)
Costa, Habdel Nasser Rocha da; Santos, Maria Cristina dos; Alcântara, Antônio Flavio de Carvalho; Silva, Marilda Conceição; França, Roberta Cabral; Pil¨®-Veloso, Dorila
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

18 .     euscaphic acid
    ÏàËÆ¶È:75.8%
Chinese Traditional and Herbal Drugs          2012          43          1285-1288
Study on chemical constituents from Potentilla supina
ZHENG Guang-hai; PIAO Hui-shun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

19 .     3,23-disulfate ester of rotundic acid
C30H48O11S2     ÏàËÆ¶È:73.3%
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

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20 .     gymnemagenol
    ÏàËÆ¶È:73.3%
Journal of Natural Products          2001          64          232-235
Antisweet Saponins from Gymnema sylvestre
Wencai Ye, Xin Liu,Qingwen Zhang,Chun-Tao Che, and Shouxun Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     3¦Â,6¦Â,19¦Á,24-tetrahydroxyurs-12-en-28-oic acid
C30H48O6     ÏàËÆ¶È:73.3%
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

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22 .     3¦Â, 6¦Â, 19¦Á-trihydroxyurs-12-en-28-oic-acid
C30H48O5     ÏàËÆ¶È:73.3%
Acta Botanica Yunnanica          1995          17(2)          209-214
TRITERPENOIDS FROM UNCARIA RHYNCHOPHYLLA
YANG Cheng-Jing, ZHANG Jim, WU Da-Gang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

23 .     compound 11
C30H50O5     ÏàËÆ¶È:73.3%
Chemical & Pharmaceutical Bulletin          1985          33          37-40
19¦Á-Hydroxyursane-Type Triterpene Glucosyl Esters from the Roots of Rubus suavissimus S. LEE
FENG GAO,FENGHUAI CHEN,TAKASHI TANAKA,RYOJI KASAI,TAKASHI SETO and OSAMU TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     compound III
    ÏàËÆ¶È:73.3%
Acta Botanica Sinica          1999          41          206-208
Structural identification of Kudinchagenin I
Wen Yong-Xin, Liang Xiao-Yan, Cheng Gui-Ren
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     3¦Â,19¦Á,23¦Â-trihydroxylurs-12-en-28-oic acid
    ÏàËÆ¶È: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
2Â¥2013-04-25 10:43:57
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