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1 .     euphadienol
C30H50O     ÏàËÆ¶È:73.9%
Phytochemistry          1995          38          233-236
Three prenylated phenolic benzophenones from Garcinia myrtifolia
Claude Spino, Jitendra Lal, Subramaniam Sotheeswaran, William Aalbersberg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     11¦Á-Aretoxy-helifulvan-19-sauremethylester
C23H34O4     ÏàËÆ¶È:65.2%
Phytochemistry          1979          18          1359-1362
Helifulvanolsäkure¡ªein neues diterpen mit anomalem kohlenstoffger¨¹st aus Helichrysum fulvum
Ferdinand Bohlmann, Christa Zdero, Reinhard Zeisberg, William S. Sheldrick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     23,24,25,26,27-pentanorlanost-8-ene-3¦Â,22,diol
    ÏàËÆ¶È:64%
Chemical & Pharmaceutical Bulletin          2000          48(10)          1422-1426
A New Pentanorlanostane Derivative, Cladosporide A, as a Characteristic Antifungal Agent against Aspergillus fumigatus, Isolated form Cladosporium sp.
Tomoo HOSOE,Hideaki OKADA,Takeshi ITABASHI,Koohei NOZAWA,Kaoru OKADA,Galba Maria de CAMPOS TAKAKI,Kazutaka FUKUSHIMA,Makoto MIYAJI and Ken-ichi KAWAI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     compound 1
    ÏàËÆ¶È:64%
Organic Magnetic Resonance          1983          21          305-309
Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers
Takashi Iida, Toshitake Tamura, Taro Matsumoto and Frederic C. Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     dapholdhamine B
C22H35NO3     ÏàËÆ¶È:63.6%
Journal of Natural Products          2009          72          1325-1327
Dapholdhamines A-D, Alkaloids from Daphniphyllum oldhami
Yu Zhang,Ying-Tong Di, Shu-Zhen Mu, Chun-Shun Li, Qiang Zhang, Cheng-Jian Tan, Zhen Zhang,Xin Fang, and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     8(9),15-Isopimaradien-3¦Â-ol
C20H32O     ÏàËÆ¶È:63.6%
Journal of Natural Products          2004          67          631-637
Labdanes and Isopimaranes from Platycladus orientalis and Their Effects on Erythrocyte Membrane and on Plasmodium falciparum Growth in the Erythrocyte Host Cells
Javad Asili, Maja Lambert, Hanne L. Ziegler, , Majid Sairafianpour, Matthias Witt, Gholamreza Asghari, Ismaiel S. Ibrahimi, and Jerzy W. Jaroszewski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     15-acetoxy-cis-clerodan-3-ene-18-al
C22H36O3     ÏàËÆ¶È:63.6%
Journal of Natural Products          2003          66          316-319
cis-Clerodane Type Diterpenes from Cistus monspeliensis1
Eleftherios Kalpoutzakis, Nektarios Aligiannis, Alexios-Leandros Skaltsounis, and Sofia Mitakou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     laingolide
    ÏàËÆ¶È:63.6%
Journal of Natural Products          1999          62          934-936
Madangolide and Laingolide A, Two Novel Macrolides from Lyngbya bouillonii (Cyanobacteria)
D. Klein, J. C. Braekman, D. Daloze, L. Hoffmann, G. Castillo, and V. Demoulin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     compound 16
C22H30O     ÏàËÆ¶È:63.6%
Phytochemistry          1998          47          363-369
Diterpenoid feeding-deterrents from Laurencia saitoi
Kazuya Kurata, Kazuya Taniguchi, Yukio Agatsuma, Minoru Suzuki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     methyl-8,9-epoxy-ent-pimara-15-en-19-oate
C21H32O3     ÏàËÆ¶È:63.6%
Phytochemistry          1992          31          2793-2796
Diterpene acids from Mikania triangularis
Frederico G. Cruz, Nidia F. Roque
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     Compound 3a
    ÏàËÆ¶È:63.6%
Bioorganic & Medicinal Chemistry Letters          2002          12          1909-1912
Synthesis and affinity studies of himbacine derived muscarinic receptor antagonists
Ling-Jie Gao, Magali Waelbroeck, Sven Hofman, Dirk Van Haver, Marco Milanesio, Davide Viterbo, Pierre J. De Clercq
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     compound 10
    ÏàËÆ¶È:63.6%
Phytochemistry          1977          16          1583-1586
Ein neues clerodan-derivat sowie weitere inhaltsstoffe aus der gattung Macowania ag
Ferdinand Bohlmann, Christa Zdero
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     4-thia-5¦Â-androstanone
C18H26OS     ÏàËÆ¶È:63.6%
Tetrahedron          2005          61          3691-3696
Shielding effect of thioether C¨CS bond from proton chemical shifts of 4-thia-5¦Á- and 4-thia-5¦Â-androstane-17-ones
Hajime Iwamoto, Takefumi Kawatani, Yoshimasa Fukazawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     compound 4
    ÏàËÆ¶È:63.6%
Tetrahedron          1996          52          2325-2336
Shielding effect of ether C¤RO bond obtained from proton chemical shifts of 4-oxa-5¦Á- and 4-oxa-5¦Â-androstan-17-ones
Yanyan Yang, Takeharu Haino, Shuji Usui, Yoshimasa Fukazawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     compound 57
    ÏàËÆ¶È:63.6%
Natural Product Communications          2008          3          399-412
Structural Elucidation of Pimarane and IsopimaraneDiterpenoids: The 13C NMR Contribution
Ana M. L. Seca, Diana C. G. A. Pinto and Artur M. S. Silva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     methyl (5R*,8S*,9S*,10R*)-cleroda-3,13-dien-15-oate
    ÏàËÆ¶È:63.6%
Journal of the Brazilian Chemical Society          2002          13          389-391
A New ent-Clerodane Diterpene from Hymenaea courbaril var. altissima
Raquel T. Nogueira, Rosana A. Giacomini, George J. Shepherd and Paulo M. Imamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     2-(Digitoxigenin-3-ylthio)ethanol
C25H38O4S     ÏàËÆ¶È:62.5%
Bioorganic & Medicinal Chemistry          2011          19          2407-2417
Synthesis and evaluation of cardiac glycoside mimics as potential anticancer drugs
Marie Jensen, Steffen Schmidt, Natalya U. Fedosova, Jan Mollenhauer, Henrik H. Jensen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     1,2-Bis(digitoxigenin-3-ylthio)ethane
C48H70O6S2     ÏàËÆ¶È:62.5%
Bioorganic & Medicinal Chemistry          2011          19          2407-2417
Synthesis and evaluation of cardiac glycoside mimics as potential anticancer drugs
Marie Jensen, Steffen Schmidt, Natalya U. Fedosova, Jan Mollenhauer, Henrik H. Jensen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     3¦Â-acetoxy-24-methyl-29-norlanost-8,25-diene
    ÏàËÆ¶È:62.5%
Phytochemistry          1988          27          3841-3843
Major triterpenes from the resins of Commiphora incisa and C. kua and their potential chemotaxonomic significance
Gordon J. provan,Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     12-Thi¦Á-3¦Á,7¦Á,24-trimethoxy-5¦Â-cholan-12,12-dioxide
C26H46O5S     ÏàËÆ¶È:61.5%
Steroids          2011          76          324-330
Synthesis of 12-oxa, 12-aza and 12-thia cholanetriols
Malika Ibrahim-Ouali, Khalil Hamze, Luc Rocheblave
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     4-Nor-3-oxo-4-oxa-5¦Á-Cholestane
C26H44O2     ÏàËÆ¶È:61.5%
Steroids          2011          76          1341-1345
Expedited Baeyer¨CVilliger oxidation of steroidal ketones by microwave irradiation
Juri Moni Borah, Pritish Chowdhury
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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