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1 .     eburicoic acid
C31H50O3     ÏàËÆ¶È:96.7%
Journal of Chinese Medicinal Materials          2011          34          549-551
Studies on the Secondary Metabolites of Coriolopsis sp.G066
SANG Zhi-gao, LI Dong-li, TAO Mei-hua, ZHANG Wei-min, TU Guo-quan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     eburicoic acid
C31H50O3     ÏàËÆ¶È:87.0%
Chinese Traditional and Herbal Drugs          2005          36          811-814
Chemical constituents of Fomes officinalis (¢ñ)
WU Xia; YANG Jun-shan; DONG Yue-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     ´óꪴ¼
    ÏàËÆ¶È:86.6%
Natural Product Research and Development          2011          23          443-445
Novel Secondary Metabolites with Cytotoxic Activities Produced by Verrucosispora sp. FIM06031 from Marine Sponge
NIE, Yi-lei, WANG, Chuan-xi, ZHENG, Yong-biao, LIN, Ru, XU, Li-yan, PENG, Fei, FANG, Dong-sheng, LIAN, Yun-yang, JIANG, Hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     acetate
C33H5204     ÏàËÆ¶È:84.8%
Chemistry of Natural Compounds          2000          36          72-75
LOW-MOLECULAR-WEIGHT MUSHROOM METABOLITES.V. EBURICOIC ACID FROM Polyporus ailanthus
L. S. Kamaiov, M. A. Agzamova,S. F. Aripova, and M. I. lsaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     obtusifoliol
    ÏàËÆ¶È:83.3%
Phytochemistry          1990          29          2513-2520
Effect on ergosterol biosynthesis of a fungicide,SSF-109,in Botrytis cinerea
Noboru Shirane,Akira Murabayashi,Michio Masuko,Atsuko Uomori,Yohko Yoshimura,Shujiro Seo,Kiyohisa Uchida,Ken'ichi Takeda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     obtusifoliol
C30H50O     ÏàËÆ¶È:83.3%
Chinese Journal of Natural Medicines          2008          6          271-274
Chemical Constituents from the Roots and Stems of Ervatamia hainanensis
JIN Li; LU Jia; JIN Yong-Sheng; YANG Xiang-Nan; CHEN Hai-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     trametenolicacid
    ÏàËÆ¶È:83.3%
Natural Product Research and Development          2010          22          433-436
Chemical Constituents and Anti-inflammatory Activities of Inonotus obliquus
ZHANG Xu; ZHAO Fen-qin; HAN Guang; LIU Lei; GAO Xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     trametenolic acid
    ÏàËÆ¶È:83.3%
Lishizhen Medicine and Materia Medica Research          2006          17          1178-1181
Chemical Constituents of Inonotus obliquus
ZHAO Fen-qin, PIAO Hui-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     3¦Â-(2-Methoxy-oxalyloxy)-24-methylene-5¦Á-lanost-8-en-21-oic acid
C34H52O6     ÏàËÆ¶È:82.3%
Journal of Asian Natural Products Research          2013          15          253-257
Two new triterpenoids from the fungus Perenniporia maackiae
Hua Guo, Jing Si, Zheng-Hui Li, Tao Feng, Ze-Jun Dong, Yu-Cheng Dai & Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     fomefficinic acid A
C31H48O3     ÏàËÆ¶È:80.6%
Chemical & Pharmaceutical Bulletin          2004          52(11)          1375-1377
New Lanostane-Type Triterpenes from Fomes officinalis
Xia WU, JunShan YANG,Liang ZHOU, and YueSheng DONG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     methyl 3¦Á,24S-dihydroxytirucalla-8,25-dien-21-oate
C31H50O4     ÏàËÆ¶È:80.6%
Phytochemistry          2006          67          1309-1315
Tirucallane triterpenes from the roots of Ozoroa insignis
Yonghong Liu , Pedro Abreu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-11-22 12:39:46
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