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1 .     3S,4S,9R,10S-11,12,14-tri-hydroxydrimene
    ÏàËÆ¶È:66.6%
China Journal of Chinese Materia Medica          2011          Vol 36,Issue 7          874-880
Studies on constituents of cultures of fungus Phellinu signiarius
WU Xiu li,LIN Sheng, ZHU Chenggen, ZHAO Feng, YU Yang, YUE Zhenggang, LIU Bo,YANG Yong chun, DAI Jungui, SHI Jiangong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     11,12,14-trihydroxydrimene
C15H26O3     ÏàËÆ¶È:66.6%
Canadian Journal of Chemistry          1889          67          1371-1380
Metabolites of the fairy ring fungus, Marasmiusoreades. Part 2. Norsesquiterpenes, further sesquiterpenes, and agrocybin
William A. Ayer, Peter Craw
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3,11,12-trihydroxydrimene
    ÏàËÆ¶È:66.6%
Canadian Journal of Chemistry          1889          67          1371-1380
Metabolites of the fairy ring fungus, Marasmiusoreades. Part 2. Norsesquiterpenes, further sesquiterpenes, and agrocybin
William A. Ayer, Peter Craw
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     7¦Â-hydroxy-10-deoxoartemisinin
C15H24O5     ÏàËÆ¶È:60%
Journal of Natural Products          2004          67          1595-1597
Hydroxylation of 10-Deoxoartemisinin by Cunninghamella elegans
Igor A. Parshikov, Kannoth M. Muraleedharan, Bruhaspathy Miriyala, Mitchell A.Avery,and John S. Williamson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (-)-11,12-dihydroxydrimene
C15H26O2     ÏàËÆ¶È:60%
The Journal of Antibiotics          1994          47          1017-1024
THE MNIOPETALS, NEW INHIBITORS OF REVERSE TRANSCRIPTASES FROM A Mniopetalum SPECIES (BASIDIOMYCETES) II. STRUCTURE ELUCIDATION
ROBERT VELTEN, DÖRTE KLOSTERMEYER, BERT STEFFAN, WOLFGANG STEGLICH, ANDREA KUSCHEL, TIMM ANKE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     7¦Â-hydroxy-10-deoxoartemisinin
    ÏàËÆ¶È:60%
Biotechnology Letters          2004          26          607-610
Hydroxylation of 10-deoxoartemisinin to 15-hydroxy-10-deoxoartemisinin by Aspergillus niger
Igor A. Parshikov, Bruhaspathy Miriyala, Mitchell A. Avery, John S. Williamson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     compound 1
C15H26O3     ÏàËÆ¶È:60%
Natural Product Communications          2008          3          1747-1750
New Drimane Sesquiterpenoids from Tidestromia oblongifolia
Sandeep Chaudhary , Vladimir Thomas, Louis Todaro, Onica LeGendre, Stevan Pecic and Wayne W. Harding
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Xerophilusin XIV
C20H34O4     ÏàËÆ¶È:60%
Archives of Pharmacal Research          2011          34          875-879
ent-Abietane Diterpenoids from Isodon xerophilus
Li Mei Li, Jian Xin Pu, Wei Lie Xiao, and Han Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     oidiolactone F
C16H22O5     ÏàËÆ¶È:56.2%
Journal of Natural Products          1999          62          1218-1221
Biologically Active Secondary Metabolites from Fungi. 12.1 Oidiolactones A-F, Labdane Diterpene Derivatives Isolated from Oidiodendron truncata
Markus John, Karsten Krohn, Ulrich Flörke, Hans-J¨¹rgen Aust, Siegfried Draeger, and Barbara Schulz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound 15
    ÏàËÆ¶È:56.2%
Phytochemistry          1994          35          713-719
Compounds with the labdane skeleton from Halimium viscosum
Julio G. Urones, Isidro S. Marcos, Pilar Basabe, David Diez, Narciso M. Garrido, Concepci¨®n Alonso, Isabel M. Oliva, Anna M. Lithgow, Rosalina F. Moro, M Jose Sexmero, Carlos Lopez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     8-desacyl-4¦Â-hydroxy-15-dihydrocarmanin
C16H26O7     ÏàËÆ¶È:56.2%
Phytochemistry          1992          31          3630-3632
Sesquiterpenes, flavonoids and lignans from Onopordon acaulon
Luz Cardona, Rafael A. Alemañ, Begoña Garcia, Jos¨¦ R. Pedro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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