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CÆ×Êý¾Ý  12.52,15.15,17.15,18.41,21.22,29.23,32.16,33.33,33.63,36.26,39.81,42.23,51.04,56.19,60.63,78.34,88.69,114.19,117.48,165.56
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Ò©Îﻯѧli: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-27 11:18:16
1 .     compound 10
C18H30O4     ÏàËÆ¶È:65%
Journal of Natural Products          1997          60          1115-1120
Sesquiterpenoids of the Drimane Class from a Sponge of the Genus Dysidea
Valerie J. Paul, Youngwan Seo, Ki Woong Cho, Jung-Rae Rho, Jongheon Shin, and Patricia R. Bergquist
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     7¦Â,12¦Á-dihydroxymanoyl oxide
C20H34O3     ÏàËÆ¶È:65%
Planta Medica          2009          75          1344-1348
Terpenoids from Roots of Chloranthus henryi
Xianwen Gan, LeiMa, Qigang Chen, Qiuqun Chen, Qiang Yu, Lihong Hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     8¦Á,15-Epoxylabdan-16¦Â-oic acid
C20H34O3     ÏàËÆ¶È:65%
Phytochemistry          2010          71          798-803
8,15-Epoxylabdane and norlabdane diterpenoids from Eragrostis viscosa
N¡¯Soki N. Sebastião, In¨ºs J.S. Cordeiro, Aldenir F. dos Santos, Jorge F. Gaspar, C¨¦lia Martins, Jos¨¦ Rueff, Carlos Diakanamwa, Antônio E.G. Sant¡¯Ana, Dina I.M.D. de Mendonça
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     acuminolide
C20H30O5     ÏàËÆ¶È:65%
Tetrahedron          1995          51          21-28
Novel cytotoxic labdane diterpenoids from Neouvaria acuminatissima
Ik-Soo Lee, Xianjian Ma, Hee-Byung Chai, Domingo A. Madulid, R. Brian Lamont, Melanie J. O'Neill, Jeffrey M. Besterman, Norman R. Farnsworth, D. Doel Soejarto, Geoffrey A. Cordell, John M. Pezzuto, A. Douglas Kinghorn
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     compound 7A2-54
    ÏàËÆ¶È:65%
Magnetic Resonance in Chemistry          1993          31          299-308
13C NMR data for labdane diterpenoids
Alejandro F. Barrero and Joaquin Altarejos
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     N-(hexahydro-2-oxo-1H-azepin-3-yl)-3-methyl-5-(1,2,6-trimethyl-2-cyclohexen-1-yl)-2-pentenamide
C21H34N2O2     ÏàËÆ¶È:61.9%
Journal of Natural Products          1993          Vol 56          500
Sesquiterpene-Derived Metabolites from the Deep Water Marine Sponge Poecillastra sollasi
K. Brian Killday, Ross Longley, Peter J. McCarthy, Shirley A. Pomponi, Amy E. Wright, Robert F. Neale, Matthew A. Sills
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     suregadolide B
C20H26O3     ÏàËÆ¶È:60%
Journal of Natural Products          2002          65          932-934
Novel Diterpene Lactones from Suregada multiflora
Ismet Ara Jahan, Nilufar Nahar, M. Mosihuzzaman, Farzana Shaheen, Zeba Parween,Atta-ur-Rahman,and M. Iqbal Choudhary
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     compound 7
C17H32O6S2     ÏàËÆ¶È:60%
Journal of Natural Products          2001          64          348-349
Synthesis of (+)-Cyclozonarone and the Absolute Configuration of Naturally Occurring (-)-Cyclozonarone
Manuel Cort¨¦s, Jaime A. Valderrama, Mauricio Cuellar, Ver¨®nica Armstrong, and Marcelo Preite
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     ((1S,2R,4aS,8aS)-5,5,8a-trimethyl-decahydronaphthalene-1,2-diyl)bis(methylene) diacetate
C19H32O4     ÏàËÆ¶È:60%
Journal of Natural Products          1996          59          866-868
Drimane Sesquiterpenes from the Sponge Dysidea fusca
A. Montagnac, M.-T. Martin, C. Debitus, and M. Païs
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     ent-15¦Â,16-epoxy-kauran-17-ol
C20H32O2     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1982          30          3922-3931
Studies on the Constituents of the Crude Drug "Fritillariae Bulbus." IV. On the Diterpenoid Constituents of the Crude Drug "Fritillariae Bulbus"
JUNICHI KITAJIMA,NAOKI NODA,YOSHITERU IDA,TETSUYA KOMORI and TOSHIO KAWASAKI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-05-26 17:53:52
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