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hanglin11

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12.8,16.3,23.2,28.5,29.5,29.7,31.9,32.2,44.5,45.1,59.1,61.5,72.6,95.4,103.1,106.7,125.4,128.2,128.5,143.6,154.3,159.8,162.6,196.4
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hanglin11

ľ³æ (ÖªÃû×÷¼Ò)

ÉÙ¸øÁËÁ½¸öÖØ¸´Ì¼Ðźţ¬12.8,16.3,23.2,28.5,29.5,29.7,31.9,32.2,44.5,45.1,59.1,61.5,72.6,95.4,103.1,106.7,125.4,128.2,128.2,128.5,128.5,143.6,154.3,159.8,162.6,196.4
2Â¥2012-11-04 12:43:22
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1 .     linderachalcone
C25H28O4     ÏàËÆ¶È:57.6%
Phytochemistry          1989          28          955-956
Two flavonoids from two Lindera umbellata varieties
Kazuhiko Ichino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     linderachalcone
    ÏàËÆ¶È:57.6%
Chemistry Letters          1989          18          363-366
Isolation and Structures of Two New Flavonoids from Lindera umbellata
Kazuhiko Ichino, Hitoshi Tanaka and Kazuo Ito
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     Lehualide E
C24H32O4     ÏàËÆ¶È:57.6%
Journal of Natural Products          2011          74          809-815
Lehualides E−K, Cytotoxic Metabolites from the Tongan Marine Sponge Plakortis sp.
Jacqueline M. Barber, Natelle C. H. Quek, Dora C. Leahy, John H. Miller, David S. Bellows, and Peter T. Northcote
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     Pyrazine-2-carboxylic acid (1-benzylcarbamoyl-pentyl)-cyclohexyl-amide
C24H32N4O2     ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry Letters          2007          17          5483-5486
Novel anti-tuberculosis agents from MCR libraries
Alexander Dömling, Sepp Achatz, Barbara Beck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     N-(3S-N-L-prolinyl-1,2,3,4-tetrahydroisoquinoline-3-carbonyl)-L-proline
C20H25N3O4     ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry          2010          18          1536-1554
2, 3-Diamino acid modifying 3S-tetrahydroisoquinoline-3-carboxylic acids: Leading to a class of novel agents with highly unfolded conformation, selective in vitro anti-platelet aggregation and potent in vivo anti-thrombotic activity
Xiaoyi Zhang, Wei Wang, Shenling Cheng, Ming Zhao, Meiqing Zheng, Heng Wei Chang, Jianhui Wu, Shiqi Peng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     Lehualide G
C25H34O4     ÏàËÆ¶È:53.8%
Journal of Natural Products          2011          74          809-815
Lehualides E−K, Cytotoxic Metabolites from the Tongan Marine Sponge Plakortis sp.
Jacqueline M. Barber, Natelle C. H. Quek, Dora C. Leahy, John H. Miller, David S. Bellows, and Peter T. Northcote
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     Myristinin D
    ÏàËÆ¶È:53.3%
Archives of Pharmacal Research          2009          32          685-692
A new acyclic diterpene acid and bioactive compounds from Knema glauca
Noppadon Rangkaew, Rutt Suttisri, Masataka Moriyasu and Kazuko Kawanishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     ramosine C
C30H38N4O5     ÏàËÆ¶È:51.8%
Helvetica Chimica Acta          2003          Vol. 86          127
14-Membered Cyclopeptides from Paliurus ramosissimus and P. hemsleyanus
Hui-yi Lin, Chung-Hsiung Chen, Karin C. S. Chen Liu, and Shoei-Sheng Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     1R,2S,3S,4S)-2-{1-[4-(tert-butyldiphenylsilyloxy)butyl]vinyl}-1,5,5-trimethyl-6-methylene-3-(phenylmethoxy)bicyclo[2.2.2]octan-2-ol
C41H54O3Si     ÏàËÆ¶È:51.7%
Australian Journal of Chemistry          2004          57          53-66
Taxane Diterpene Synthesis Studies. Part 2: Towards Taxinine¡ªEnantiospecific Construction of an AB-ring Substructure Incorporating both Quaternary Carbon Centres and Attempts to Annulate the C-ring
Martin G. Banwell , Malcolm D. McLeod and Andrew G. Riches
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     notoamide K
C26H31N3O5     ÏàËÆ¶È:50%
Journal of Natural Products          2008          71(12)          2064-2067
Notoamides F-K, Prenylated Indole Alkaloids Isolated from a Marine-Derived Aspergillus sp.
Sachiko Tsukamoto, Hikaru Kato, Masayuki Samizo, Yuka Nojiri, Hiroyuki Onuki, Hiroshi Hirota, and Tomihisa Ohta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2012-11-04 13:03:07
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