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15.3, 15.8, 16.0, 16.2, 17.9, 21.7, 22.6, 23.1, 23.9, 25.0, 27.7, 30.2, 31.9, 33.1, 37.1, 37.7, 39.0, 39.3, 39.5, 41.3, 41.5, 42.0, 44.0, 55.1, 64.4, 65.5, 73.2, 103.8, 122.0, 125.6, 138.0, 143.9, 153.1.
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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

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1 .     compound 230
    ÏàËÆ¶È:72.7%
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
2 .     compound 255
    ÏàËÆ¶È:72.7%
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
3 .     2¦Á,3¦Á,24-ÈýôÇ»ù-12-Ï©-28-ÎÚËÕËá(2¦Á,3¦Á,24-trihydr-oxyurs-12-en-28-oic acid)
    ÏàËÆ¶È:72.7%
Chinese Traditional and Herbal Drugs          2011          42(5)          841-843
Chemical constituents in root of Actinidia chinensis
CHEN Xiao-xiao, YANG Shang-jun, BAI Shao-yan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     methyl 2¦Á,3¦Á,24-trihydroxyursa-12,20(30)-dien-28-oate
C37H54O8     ÏàËÆ¶È:72.7%
Phytochemistry          1987          26          1107-1111
Pentacyclic triterpenoids from Prunella vulgaris
Hisashi Kojima,Hideo Tominaga,Shigeki Sato,Haruo Ogura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     methyl 2¦Á,3¦Á,24-trihydroxyurs-12-en-28-oate
C31H50O5     ÏàËÆ¶È:72.7%
Phytochemistry          1987          26          1107-1111
Pentacyclic triterpenoids from Prunella vulgaris
Hisashi Kojima,Hideo Tominaga,Shigeki Sato,Haruo Ogura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     compound 2
    ÏàËÆ¶È:72.7%
Phytochemistry          1981          20          2436-2438
13C nmr spectra of some serjanic acid derivatives
M. Alvarado, M. Moreno, V. M. Rodr¨ªguez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     compound 5e
C33H52O6     ÏàËÆ¶È:72.7%
Phytochemistry          1983          22          2547-2552
Terpenoids of Rhododendron japonicum
Jinsaku Sakakibara, Toyo Kaiya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     30-chloro-3¦Â-acetoxy-22¦Á-hydroxyl-20(21)-taraxastene
C32H51O3Cl     ÏàËÆ¶È:72.7%
Molecules          2012          17          12895-12909
Secondary Metabolites from Two Species of Tolpis and Their Biological Activities
Jorge Triana, Mariana L¨®pez, Francisco Javier P¨¦rez, Milagros Rico, Aroa L¨®pez, Francisco Est¨¦vez, Mar¨ªa Teresa Marrero, Ignacio Brouard and Francisco Le¨®n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     3-Oacetyloleanolic acid
    ÏàËÆ¶È:72.7%
Journal of Chinese Medicinal Materials          2011          34          1540-1544
Study on the Triterpenoids from the Fruits of Ligustrum lucidum
FENG Jing, FENG Zhi-yi, WANG Jun-ming, CUI Ying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound 1a
    ÏàËÆ¶È:70.5%
Journal of Natural Products          1985          Vol 48          128-131
Secondary Metabolites from Satureja Species. New Triterpenoid from Satureja acinos
Javier Escudero, J. Crist¨®bal L¨®pez, Rosa Maria Rabanal, Serafi¨½ Valverde
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     3¦Â-acetoxy-20-taraxasten-22¦Á-ol
C32H52O3     ÏàËÆ¶È:69.6%
Journal of Natural Products          2000          63          898-901
Taraxastane-Type Triterpenes from the Aerial Roots of Ficus microcarpa
Y. M. Chiang and Y. H. Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     3¦Â-O-{¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl-(1¡ú4)-[¦Â-D-glucopyranosyl-(1¡ú2)]-¦Á-L-arabinopyranosyl}-28,30-dihydroxyolean-12-ene
C53H88O21     ÏàËÆ¶È:69.6%
Planta Medica          2009          75          70-75
Triterpenoid Saponins from Ardisia pusilla and their Cytotoxic Activity
Ye Tian, Hai-Feng Tang, Feng Qiu, Xiao-JuanWang, Xiao-Li Chen, Ai-DongWen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Oleanolic acid
C30H48O3     ÏàËÆ¶È:69.6%
Chemistry of Natural Compounds          2004          40          137-140
PHYTOCHEMICAL STUDIES OF Berberis vulgaris
S. Saied and S. Begum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     3¦Â,24-Dihydroxyurs-12-en-28-oic acid methyl ester
C31H50O4     ÏàËÆ¶È:69.6%
Journal of Natural Products          1987          Vol 50          63
Plant Anticancer Agents, XLIV. Cytotoxic Constituents from Stizophyllum riparium
Chang-Yih Duh, John M. Pezzuto, A. Douglas Kinghorn, Sai L. Leung, Norman R. Farnsworth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     soyasapogenol B
    ÏàËÆ¶È:69.6%
Journal of Natural Products          1990          Vol 53          298
Sapogenin Structure: Analysis of the 13C- and 1H-nmr Spectra of Soyasapogenol B
Robert L. Baxter, Keith R. Price, G. Roger Fenwick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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2Â¥2013-12-23 16:21:12
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