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²éѯ½á¹û£º¹²²éµ½14432¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ |
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