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13C NMR (151 MHz, DMSO) ¦Ä = 172.1, 134.8, 131.1, 130.9, 130.6, 129.1, 123.6, 103.56, 76.9, 76.6, 73.4, 71.96, 70.6, 70.0, 68.8, 61.1, 52.9, 48.7, 39.5, 32.2, 31.8, 31.7, 29.3, 29.2, 29.1, 28.9, 27.6, 27.4, 22.2, 15.7, 13.9, 13.9.
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jiangchunyong: ½ð±Ò+1, лл 2013-03-01 13:30:19
star_lgp: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-03-01 14:40:18
1 .     alternaroside B
C42H77NO9     ÏàËÆ¶È:93.5%
Journal of Natural Products          2009          72          1695-1698
Cerebrosides of the Halotolerant Fungus Alternaria raphani Isolated from a Sea Salt Field
Wenliang Wang, Yi Wang, Hongwen Tao, Xiaoping Peng, Peipei Liu, and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     Chrysogeside B
C41H75NO9     ÏàËÆ¶È:90.6%
Journal of Natural Products          2011          74          1298-1302
Cerebrosides and 2-Pyridone Alkaloids from the Halotolerant Fungus Penicillium chrysogenum Grown in a Hypersaline Medium
Xiaoping Peng, Yi Wang, Kunlai Sun, Peipei Liu, Xia Yin, and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     Chrysogeside C
C40H73NO9     ÏàËÆ¶È:90.3%
Journal of Natural Products          2011          74          1298-1302
Cerebrosides and 2-Pyridone Alkaloids from the Halotolerant Fungus Penicillium chrysogenum Grown in a Hypersaline Medium
Xiaoping Peng, Yi Wang, Kunlai Sun, Peipei Liu, Xia Yin, and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     (2S,2'R,3R,3'E,4E,8E)-1-O-¦Â-D-glucopyranosyl-2-N-(2'-hy-droxy-3'-octadecenoyl)-3-hydroxy-9-methyl-4,8-sphingadienine
C43H79NO9     ÏàËÆ¶È:87.5%
Lipids          2004          39          667-673
Antibacterial and xanthine oxidase inhibitory cerebrosides from Fusarium sp. IFB-121, and endophytic fungus in Quercus variabilis
R. G. Shu, F. W. Wang, Y. M. Yang, Y. X. Liu and R. X. Tan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     Chrysogeside D
C43H79NO9     ÏàËÆ¶È:85.2%
Journal of Natural Products          2011          74          1298-1302
Cerebrosides and 2-Pyridone Alkaloids from the Halotolerant Fungus Penicillium chrysogenum Grown in a Hypersaline Medium
Xiaoping Peng, Yi Wang, Kunlai Sun, Peipei Liu, Xia Yin, and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




6 .     alternaroside A
C43H77NO10     ÏàËÆ¶È:81.2%
Journal of Natural Products          2009          72          1695-1698
Cerebrosides of the Halotolerant Fungus Alternaria raphani Isolated from a Sea Salt Field
Wenliang Wang, Yi Wang, Hongwen Tao, Xiaoping Peng, Peipei Liu, and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




7 .     Chrysogeside E
C41H77NO9     ÏàËÆ¶È:81.2%
Journal of Natural Products          2011          74          1298-1302
Cerebrosides and 2-Pyridone Alkaloids from the Halotolerant Fungus Penicillium chrysogenum Grown in a Hypersaline Medium
Xiaoping Peng, Yi Wang, Kunlai Sun, Peipei Liu, Xia Yin, and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




8 .     alternaroside C
C42H77NO9     ÏàËÆ¶È:77.4%
Journal of Natural Products          2009          72          1695-1698
Cerebrosides of the Halotolerant Fungus Alternaria raphani Isolated from a Sea Salt Field
Wenliang Wang, Yi Wang, Hongwen Tao, Xiaoping Peng, Peipei Liu, and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




9 .     Chrysogeside A
C40H73NO9     ÏàËÆ¶È:77.4%
Journal of Natural Products          2011          74          1298-1302
Cerebrosides and 2-Pyridone Alkaloids from the Halotolerant Fungus Penicillium chrysogenum Grown in a Hypersaline Medium
Xiaoping Peng, Yi Wang, Kunlai Sun, Peipei Liu, Xia Yin, and Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




10 .     (2S,2'R,3R,3'E,4E,8E,10E)-1-O-¦Â-D-glucopyranosyl-2-N-(2'-hydroxy-3'-octadecenoyl)-3-hydroxy-9-methyl-4,8,10-sphingatrienine
C43H77NO9     ÏàËÆ¶È:76.6%
Lipids          2004          39          667-673
Antibacterial and xanthine oxidase inhibitory cerebrosides from Fusarium sp. IFB-121, and endophytic fungus in Quercus variabilis
R. G. Shu, F. W. Wang, Y. M. Yang, Y. X. Liu and R. X. Tan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




11 .     1-O-¦Â-D-glucopyranosyl(2S,3S,4R,8E)-2-[(2'R)-2'-hydroxytetra cosanamino]-8-octadecene-1,3,4-triol
    ÏàËÆ¶È:70%
Natural Product Research and Development          2005          17          298-300
Studies on Chemical Constituents of Polygala aureocauda
HUANG Zhao-hui; XU Kang-ping; ZHOU Ying-jun; HU Gao-yun; TAN Gui-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     cerebroside B
C41H77NO9     ÏàËÆ¶È:69.6%
Chinese Traditional and Herbal Drugs          2004          35          493-495
È˹¤Ó¼³æ²Ý»¯Ñ§³É·ÖÑо¿
Íõ¸Õ,Âé±ø¼Ì,Áõ¼ª¿ª
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




13 .     1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E)-2-[(2'R)-2'-hydroxypalmitoyl amino]-8-octadecene-1,3,4-triol
    ÏàËÆ¶È:66.6%
Natural Product Research and Development          2005          17          298-300
Studies on Chemical Constituents of Polygala aureocauda
HUANG Zhao-hui; XU Kang-ping; ZHOU Ying-jun; HU Gao-yun; TAN Gui-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E)-2-[(2'R)-2'-hydroxy-tetracosanoyl]-8-octadecene-1,3,4-triol
C48H93NO10     ÏàËÆ¶È:63.3%
Chinese Journal of Natural Medicines          2009          7          115-118
Chemical Constituents from the Fruits of Ziziphus jujuba
GUO Sheng; TANG Yu-Ping; DUAN Jin-Ao; SU Shu-Lan; QIAN Da-Wei Jiangsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     1-(C-lactosyl)nonadecan-2-one
C31H58O11     ÏàËÆ¶È:62.5%
European Journal of Organic Chemistry          2010                   1314-1323
Horner¨CWadsworth¨CEmmons Reaction of Unprotected Sugars in Water or in the Absence of Any Solvent: One-Step Access to C-Glycoside Amphiphiles
Adeline Ranoux, Loïc Lemi¨¨gre, Maud Benoit, Jean-Paul Gu¨¦gan and Thierry Benvegnu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     Buteagibrenol Glycoside
C27H48O11     ÏàËÆ¶È:60%
Chemistry of Natural Compounds          2010          46          44-48
Phytochemical investigation of the seeds of Butea monosperma
S. Alam, M. Ali, P. Alam and M. Shuaib
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     thuggacin A
C35H53NSO7     ÏàËÆ¶È:57.1%
Chemistry-A European Journal          2007          13          5822-5832
Thuggacins, Macrolide Antibiotics Active against Mycobacterium tuberculosis: Isolation from Myxobacteria, Structure Elucidation, Conformation Analysis and Biosynthesis
Heinrich Steinmetz, Herbert Irschik, Brigitte Kunze, Hans Reichenbach, Gerhard Höfle and Rolf Jansen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     Shanyenoside E
C30H44O14     ÏàËÆ¶È:53.3%
Planta Medica          2012          78          1967-1971
Isolation of Antithrombotic Phenolic Compounds from the Leaves of Crataegus pinnatifida
Song, Shao-Jiang; Li, Ling-Zhi; Gao, Pin-Yi; Yuan, Yan-Qiang; Wang, Ru-Ping; Liu, Ke-Chun; Peng, Ying:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     canarigenin-3-O-¦Á-L-rhamnopyranosyl-(1¡ú5)-O-¦Â-D-xylofuranoside
C34H50O12     ÏàËÆ¶È:52.9%
Journal of Natural Products          1992          Vol 55          39
A Novel Cardenolide, Canarigenin-3-O-¦Á-L-rhamnopyranosyl-(1¡ú5)-O-¦Â-D-xylofuranoside, from Rhizomes of Convallaria majalis
V. K. Saxena, P. K. Chaturvedi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     ((S)-2,2-dimethyl-1-oxo-1-((S)-2-oxoazepan-3-ylamino)decan-3-yl) 6-(N-(Hydroxy)formamido)-(2S)-2-(5-methyl-2-phenylox-azole-4-carboxamido)hexanoate
C36H53N5O8     ÏàËÆ¶È:51.6%
The Journal of Organic Chemistry          2008          73          1018-1024
Syntheses and Biological Activity of Amamistatin B and Analogs
Kelley A. Fennell, Ute Möllmann, and Marvin J. Miller
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     thuggacin C
C35H53NSO7     ÏàËÆ¶È:51.4%
Chemistry-A European Journal          2007          13          5822-5832
Thuggacins, Macrolide Antibiotics Active against Mycobacterium tuberculosis: Isolation from Myxobacteria, Structure Elucidation, Conformation Analysis and Biosynthesis
Heinrich Steinmetz, Herbert Irschik, Brigitte Kunze, Hans Reichenbach, Gerhard Höfle and Rolf Jansen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     carteriosulfonic acid C
C34H65NO10S     ÏàËÆ¶È:50%
Journal of Natural Products          2009          72          1651-1656
Carteriosulfonic Acids A-C, GSK-3¦ÂInhibitors from a Carteriospongia sp.
Malcolm W. B. McCulloch, Tim S. Bugni, Gisela P. Concepcion, Gary S. Coombs, Mary Kay Harper, Simran Kaur,Gina C. Mangalindan, Misha M. Mutizwa, Charles A. Veltri, David M. Virshup, and Chris M. Ireland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     Hyrcanoside
    ÏàËÆ¶È:50%
Journal of Natural Products          1979          Vol 42          293-298
Potential Antitumor Agents: A Cytotoxic Cardenolide From Coronilla varia
Johnny A. Hembree, C.-J. Chang, Jerry L. McLaughlin, Garnet Peck, John M. Cassady
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     SQGD
C37H69O12SNa     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry Letters          2010          20          6699-6702
Identification of a sulfonoquinovosyldiacylglyceride from Azadirachta indica and studies on its cytotoxic activity and DNA binding properties
Ratna Chatterjee, Omkar Singh, Lalawmpuii Pachuau, Shiba Prasad Malik, Mausumi Paul, Kakali Bhadra, Santanu Paul, Gopinatha Suresh Kumar, Nirup Bikash Mondal, Sukdeb Banerjee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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