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nevafgb51: ½ð±Ò+10 2015-05-27 17:00:31
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nevafgb51: ½ð±Ò+10 2015-05-27 17:00:31
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1 . 20R-24¦Â-hydroxyl-20,25-epoxydamar-3-one ÏàËÆ¶È:73.3% Chemistry and Industry of Forest Products 2013 33 121-127 Chemical Constituents of the Branches of Ailanthus altissima Swingle LIU Ji-mei, ZHANG Zhong-wei, YAO Jia, WANG Jin-lan, ZHAO Ming, ZHANG Shu-jun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 20(R)-hydroxydammara-24-en-3-one C30H52O4 ÏàËÆ¶È:70% Chinese Traditional and Herbal Drugs 2014 45 161-163 A new dammatane-type triterpene from root barks of Ailanthus altissima WANG Le-fei, ZHAO jun, TANG Wen-zhao, WANG Xiao-jing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . quercinic acid C methyl ester C32H52O5 ÏàËÆ¶È:67.7% Phytochemistry 2005 66 1656-1661 Lanostane triterpenoids from the inedible mushroom Fomitopsis spraguei Dang Ngoc Quang, Yuuki Arakawa, Toshihiro Hashimoto, Yoshinori Asakawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . fomitopinic acids A C30H48O5 ÏàËÆ¶È:66.6% Journal of Natural Products 2005 68 69-73 Lanostane Triterpenoids and Triterpene Glycosides from the Fruit Body of Fomitopsis pinicola and Their Inhibitory Activity against COX-1 and COX-2 Kazuko Yoshikawa, Megumi Inoue, Yuki Matsumoto, Chika Sakakibara,Hideki Miyataka, Hitoshi Matsumoto, and Shigenobu Arihara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . hypocrellol C C30H46O3 ÏàËÆ¶È:66.6% Journal of Natural Products 2011 74 2143−2150 Lanostane and Hopane Triterpenes from the Entomopathogenic Fungus Hypocrella sp. BCC 14524 Masahiko Isaka, Panida Chinthanom, Malipan Sappan, Rungtiwa Chanthaket,J. Jennifer Luangsa-ard, Samran Prabpai, and Palangpon Kongsaeree Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . Gardaubryone C C30H52O4 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2011 94 656-661 Dammarane Triterpenes from Gardenia aubryiVieill. Raphaël Grougnet, Prokopios Magiatis, Sofia Mitaku, Alexios-Leandros Skaltsounis, Pierre Cabalion, François Tillequin and Sylvie Michel Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . ricinodol D C30H48O4 ÏàËÆ¶È:66.6% RSC Advances 2015 5 26777−26784 Ricinodols A¨CG: new tetracyclic triterpenoids as 11b-HSD1 inhibitors from Ricinodendron heudelotii Jin-Hai Yu, Yu Shen, Yan Wu, Ying Leng, Hua Zhang and Jian-Min Yue Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . alisol A 24-acetate ÏàËÆ¶È:65.6% Natural Product Research and Development 2002 14(4) 5-8 TWO NOVEL TERPENOIDS FROM ALISMA ORIENTALIS JUZEP. PENG Guo ping; ZHU Guo yuan; LOU Feng chang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 16-oxo-24-acetate alisol A C32H50O7 ÏàËÆ¶È:65.6% Chinese Traditional and Herbal Drugs 2014 45 4356-4359 Chemical constituents from Alisma orientalis extracts with hypoglycemic effect XU Wen, , LUO Fen-rong, ZHAO Wan-li, LI Xiao-yan, LI Xue-jun, LIU Can-kun, YU Zhi-wen, WU Shui-sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . A-M2-2 ÏàËÆ¶È:65.6% Chemical & Pharmaceutical Bulletin 2008 56 41-45 Stability and Structure Studies on Alisol A 24-Acetate Bolat Makabel, Yuying Zhao, Bin Wang, Yanjing Bai, Qingying Zhang, Li Wu, Yang Lv Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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