| ²é¿´: 223 | »Ø¸´: 1 | |||
star_lgpÒø³æ (СÓÐÃûÆø)
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[ÇóÖú]
ÇóÖú΢Æ×Êý¾ÝÒ»¸ö£¡
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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
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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
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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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ |

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