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13C NMR (400MHz,DMSO) ¦Ä:14.60,16.71,20.38,24.57,25.56,27.45,28.15,30.93,32.08,40.15,44.57,45.55,48.22,68.91,72.23,94.19,123.84,129.36,130.14,135.70,168.03,206.99,209.09.
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1 .     rel-(l' R,4' S,S' R)-2-(l'-Farnesyl)-4' ,5'-dihydroxy-2'-oxocyclohexan-1'-yl)-acetic acid ¦Ä-lactone
C23H34O4     ÏàËÆ¶È:65.2%
Phytochemistry          1995          40          1723-1728
Further farnesyl-homogentisic acid derivatives from Otoba parvifolia
A. Gilberto Ferreira, João B. Fernandes, Paulo C. Vieira, Otto R. Gottlieb, Hugo E. Gottlieb
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3-(hydroxymethyl)-1,13,15-trihydroxy-7,11,15-trimethyl-2,6,10-hexadecatrien-14-yl acetate
C22H38O6     ÏàËÆ¶È:60.8%
Journal of Asian Natural Products Research          2012          14          652-656
Three new acyclic diterpenoids from Eupatorium lindleyanum DC.
Shuang-Qing Wu, Nai-Yu Xu, Jian Zhang, Shi Yao & Chun-Jun Chu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     [1S-[1¦Á,2¦Á(Z),3¦Á,4¦Á]]-7-[3-[[[[(1-thioxoheptyl)amino]acetyl]amino]rnethyl]-7-oxabicyclo[2.2.1]hept-2-yl]-5-heptenoic acid
C23H38N2O4S     ÏàËÆ¶È:60.8%
Journal of Medicinal Chemistry          1990          33          2465-2476
7-Oxabicyclo[2.2.1]heptyl carboxylic acids as thromboxane A2 antagonists: aza .omega.-chain analogs
Masami Nakane, Joyce A. Reid, Wen Ching Han, Jagabandhu Das, Vu Chi Truc, Martin F. Haslanger, Dianne Garber, Don N. Harris, Anders Hedberg,
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     homaxinone A
C19H28O2     ÏàËÆ¶È:56.5%
Journal of Natural Products          2004          67          721-724
New Cytotoxic Metabolites from a Marine Sponge Homaxinella sp.
Tayyab A. Mansoor, Jongki Hong, Chong-O. Lee, Chung Ja Sim, Kwang Sik Im, Dong Seok Lee, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (+)-17-oxocycloprotobuxine
C23H37NO     ÏàËÆ¶È:56.5%
Journal of Natural Products          1999          62          665-669
New Steroidal Alkaloids from the Roots of Buxus sempervirens
Atta-ur-Rahman, Athar Ata, Samina Naz, M. Iqbal Choudhary, Bilge Sener, and Songul Turkoz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     ent-7¦Á-acetoxy-3¦Â,12¦Á,17-trihydroxybeye¦Á-15-ene
C22H34O5     ÏàËÆ¶È:56.5%
Journal of Natural Products          1997          60          86-92
Biotransformation of ent-Atisenes and ent-Beyerenes by Rhizopus nigricans and Fusarium moniliforme Cultures
Andr¨¦s Garc¨ªa-Granados, Andr¨¦s Parra, and Jos¨¦Mar¨ªa Arias
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3¦Â,11-dihydroxy-9,11-seco-5¦Á-pregna-11,20-dihydropyran-9-one 3-acetate
C23H34O5     ÏàËÆ¶È:56.5%
Steroids          2010          75          834-847
Synthesis of cytotoxic novel 9,11-secosterol analogs: Structure/activity studies
Boonsong Kongkathip, Anuch Hasakunpaisarn, Suthinee Boonananwong, Ngampong Kongkathip
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 26
    ÏàËÆ¶È:56.5%
Phytochemistry          1998          47          1583-1600
Diterpenes from Euphorbia segetalis
J. Jakupovic, F. Jeske, T. Morgenstern, F. Tsichritzis, J. A. Marco, W. Berendsohn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     aphidicolin 17-acetate
C22H26O5     ÏàËÆ¶È:56.5%
Phytochemistry          1994          36          1551-1552
The isolation of 16¦Â, 18-dihydroxyaphidicolan-17-oic acid from Cephalosporium aphidicola
James R. Hanson, Jacqueline A. Takahashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Henrylactone B
C24H30O7     ÏàËÆ¶È:56.5%
Planta Medica          2010          76          152-158
Henrylactones A¨CE and Anti-HBV Constituents from Illicium henryi
Liu, Ji-Feng; Jiang, Zhi-Yong; Zhang, Quan; Shi, Yao; Ma, Yun-Bao; Xie, Ming-Jin; Zhang, Xue-Mei; Chen, Ji-Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 6
    ÏàËÆ¶È:56.5%
Acta Chemica Scandinavica          1986          40          855-860
Tobacco Chemistry. 63. Syntheses and Stereostructures of Six Tobacco Seco-Cembranoids.
Wahlberg, Inger; Arndt, Rolf; Nishida, Toshiaki; Enzell, Curt R.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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