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nevafgb51: ½ð±Ò+10 2015-05-27 17:00:31
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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×Ä£Äâͼ
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