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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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meitianyxs: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú 2014-09-02 19:36:58
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½581¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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