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16.13,16.83,16.91,17.01,18.70,24.25,24.33,26.08,26.54,26.79,29.06,33.01,33.16,38.48,42.58,65.77,68.89,69.20,73.05,77.70,80.62,139.66,180.81,181.92
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monkey514: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ·Ç³£¸Ðл£¡ 2013-03-12 10:54:52
1 .     tormentic acid
    ÏàËÆ¶È:62.0%
Phytochemistry          1992          31          3909-3914
Triterpenoids from plants of the sanguisorbeae
Gesa Reher, Miloš Bud¨§š¨ªnsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     nervoyan B
C24H42O6     ÏàËÆ¶È:54.1%
Biochemical Systematics and Ecology          2011          39          700-703
Phytane and neoclerodane diterpenes from the aerial parts of Inula nervosa Wall.
Lan Yan, Xiang Rong Cheng, Qi Zeng, Jiang Jiang Qin, Wei Dong Zhang, Hui Zi Jin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     aphidicolin
    ÏàËÆ¶È:54.1%
Journal of the Brazilian Chemical Society          2011          22          80-85
Biosynthesis of Aphidicolin Proceeds via the Mevalonate Pathway in the Endophytic Fungus Nigrospora sphaerica
Adriana A. Lopes and Mônica T. Pupo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (4R*,5R*,9S*,10R*,11Z)-4-methoxy-9-((dimethylamino)-methyl)-12,15-epoxy-11(13)-en-decahydrona phthalen-16-ol
C24H43O3N     ÏàËÆ¶È:54.1%
Marine Drugs          2012          10          1619-1630
A Great Barrier Reef Sinularia sp. Yields Two New Cytotoxic Diterpenes
Anthony D. Wright, Jonathan L. Nielson, Dianne M. Tapiolas, Catherine H. Liptrot and Cherie A. Motti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     ursolic acid
    ÏàËÆ¶È:53.8%
Food Chemistry          2011          124          468-475
Analysis of the anti-inflammatory properties of Rosmarinus officinalis L. in mice
Juc¨¦lia Pizzetti Beninc¨¢, Juliana Bastos Dalmarco, Moacir Geraldo Pizzolatti, Tania Silvia Fröde
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Asiatic acid
    ÏàËÆ¶È:51.8%
Archives of Pharmacal Research          2005          28          1135-1141
Inhibitory effect on TNF-¦Á-induced IL-8 production in the HT29 cell of constituents from the leaf and stem ofWeigela subsessilis
Phuong Thien Thuong, WenYi Jin, JongPill Lee, RackSeon Seong and Young-Mi Lee, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (25S)-5¦Á-cholestane-3¦Â,4¦Â,6¦Á,7¦Á,8,15¦Á,16¦Â,26-octo1
    ÏàËÆ¶È:51.8%
European Journal of Organic Chemistry          1988          1988          1185-1189
Biologically active glycosides from asteroidea, XVIII. 1H-NMR spectroscopy and biological activities of polyhydroxylated steroids from the starfish Asterina pectinifera M¨¹ller et Troschel
Ryuichi Higuchi, Yuko Noguchi, Tetsuya Komori and Takuma Sasaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (3¦Á,4¦Â,14RS)-neoclerod-13(16)-ene-3,4,14,15-tetrol
C20H36O4     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2004          Vol. 87          1279
Neoclerodane Diterpenes from Amoora stellato-squamosa
Shu-Min Yang, Shao-Hua Wu, Xiang-Dong Qin, Xiao-Dong Luo, and Da-Gang Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     ent-2¦Á,15,16,19-tetrahydroxypima¦Á-8(14)-ene
C20H34O4     ÏàËÆ¶È:50%
Journal of Natural Products          2004          67          1517-1521
Novel Diterpenoids and Diterpenoid Glycosides from Siegesbeckia orientalis
Ying Xiang, Hua Zhang, Cheng-Qi Fan, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     malacosterone
C27H44O8     ÏàËÆ¶È:50%
Phytochemistry          1998          49          2109-2114
Ecdysteroid constituents of the mushroom Tapinella panuoides
Karel Vok¨¢, Milo Budnsky, Juraj Harmath¦Á, Jitka Kohoutov¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     ursolic acid
    ÏàËÆ¶È:50%
Phytochemistry          1992          31          3909-3914
Triterpenoids from plants of the sanguisorbeae
Gesa Reher, Miloš Bud¨§š¨ªnsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     compound-3
    ÏàËÆ¶È:50%
Phytochemistry          1988          27          2205-2208
Sesquiterpene glycosides based on the alloaromaden-drane skeleton from Calendula arvensis
Cosimo Pizza,Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     compound 4a
    ÏàËÆ¶È:50%
Journal of the Chemical Society, Perkin Transactions 1          1989                   823-826
Structure elucidation of (22E,24R,25R)-24-methyl-5¦Á-cholest-22-ene-3¦Â,4¦Â,5,6¦Á,8,14,15¦Á,25,26-nonaol and (22E,24S)-24-methyl¨C5¦Á-cholest-22-ene-3¦Â,4¦Â,5,6¦Á,8,14,15¦Á,25,28-nonaol, minor marine polyhydroxysteroids isolated from the starfish Archaster typicus
Raffaele Riccio, Mos¨¦ Santaniello, Olinda Squillace Greco and Luigi Minale
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     AP1
    ÏàËÆ¶È:50%
Natural Toxins          1999          7          31-38
Oxidative deamination of hydrolyzed fumonisin B1 (AP1) by cultures of Exophiala spinifera
Barbara A. Blackwell, Jacob T. Gilliam, Marc E. Savard, J. David Miller and Dr. Jonathan P. Duvick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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