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13C NMR (101 MHz, MeOD) ¦Ä: 13.5, 22.5, 24.9, 29.0, 29.2, 29.4, 29.4, 29.5, 29.5, 31.78, 32.0, 32.4, 34.5, 53.1, 61.3, 68.3, 70.1, 71.6, 71.9, 73.5, 76.4, 77.8, 103.1, 129.2, 129.4, 130.8, 133.5, 162.1, 175.8.
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meitianyxs: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú 2014-09-02 19:36:58
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1 .     (2S,3R,4E,8E,2'R-)-1-O-(¦Â-D-Glucopyranosyl)-N-(2'-hydroxyhexadecanoyl)-4,8-sphinyadienine
    ÏàËÆ¶È:89.6%
European Journal of Organic Chemistry          1988          1988          807-814
Synthesis of sphingosine relatives, VII. Synthesis of anti-ulcerogenic cerebrosides isolated from Tetragonia tetragonoides
Kenji Mori and Takeshi Kinsho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (2S,3R,4E,8 Z,2'R)-1-O-(¦Â-D-Glucopyranosyl)-N-(2'-hydrox yhexadecanoyl)-4,8-sphingadienin
    ÏàËÆ¶È:86.2%
European Journal of Organic Chemistry          1988          1988          807-814
Synthesis of sphingosine relatives, VII. Synthesis of anti-ulcerogenic cerebrosides isolated from Tetragonia tetragonoides
Kenji Mori and Takeshi Kinsho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     triumfettoside Ic
C42H73NO9     ÏàËÆ¶È:79.3%
Helvetica Chimica Acta          2008          Vol. 91          1326
Triumfettamide and Triumfettoside Ic, Two Ceramides and Other Secondary Metabolites from the Stems of Wild Triumfetta cordifolia A. Rich. (Tiliaceae)
Louis Pergaud Sandjo, Paul Hannewald, Mehdi Yemloul, Gilbert Kirsch, and Bonaventure Tchaleu Ngadjui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     magnolioside
    ÏàËÆ¶È:78.1%
Bulletin of the Academy of Military Medical Sciences          2013          37          279-282
Chemical constituents from Solanum lyratum Thunb. ( ¢ò)
YIN Hai-long, LI Jian, DONG Jun-xing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     1-O-¦Â-D-glucopyranosyl-(2S,3R,4E,8Z)-2-N-palmitoyloctadecasphinga-4,8-dienine
C40H75NO8     ÏàËÆ¶È:76.6%
Journal of Natural Products          1997          60          274-276
New Antihepatotoxic Cerebroside from Lycium chinense Fruits
Sun Yeou Kim, Young-Hee Choi, Hoon Huh, Jinwoong Kim, Young Choong Kim, and Heum Sook Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E)-2-[(2'R)-2'-hydroxypalmitoyl amino]-8-octadecene-1,3,4-triol
    ÏàËÆ¶È:75.8%
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
7 .     1-O-¦Â-D-glucopyranosyl(2S,3S,4R,8E)-2-[(2'R)-2'-hydroxytetra cosanamino]-8-octadecene-1,3,4-triol
    ÏàËÆ¶È:73.3%
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
8 .     1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E)-2-[(2'R)-2'-hydroxy-tetracosanoyl]-8-octadecene-1,3,4-triol
C48H93NO10     ÏàËÆ¶È:72.4%
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
9 .     compound 4
C36H66O9     ÏàËÆ¶È:72.4%
Bioorganic & Medicinal Chemistry          2013          21          6554-6564
Synthesis and anti-tumor activity of carbohydrate analogues of the tetrahydrofuran containing acetogenins
Stewart Bachan, K.A. Tony, Akira Kawamura, Diego Montenegro, Anjali Joshi, Himanshu Garg, David R. Mootoo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Ophidiacerebroside C
C47H87NO9     ÏàËÆ¶È:72.4%
The Journal of Organic Chemistry          1994          59          144-147
Ophidiacerebrosides: cytotoxic glycosphingolipids containing a novel sphingosine from a sea star
Wenzao Jin, Kenneth L. Rinehart, Elizabeth A. Jares-Erijman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     alternaroside C
C42H77NO9     ÏàËÆ¶È:70.9%
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
12 .     Chrysogeside A
C40H73NO9     ÏàËÆ¶È:70.9%
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
13 .     Buteagibrenol Glycoside
C27H48O11     ÏàËÆ¶È:68.9%
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
14 .     (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:68.9%
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
15 .     Ophidiacerebroside E
C49H89NO9     ÏàËÆ¶È:68.9%
The Journal of Organic Chemistry          1994          59          144-147
Ophidiacerebrosides: cytotoxic glycosphingolipids containing a novel sphingosine from a sea star
Wenzao Jin, Kenneth L. Rinehart, Elizabeth A. Jares-Erijman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
2Â¥2014-09-02 19:08:40
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meitianyxs

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2Â¥: Originally posted by wangkaibo123 at 2014-09-02 19:08:40
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