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| 13C NMR (101 MHz, Pyr) ¦Ä: 15.5, 24.2, 27.2, 27.4, 28.6, 28.8, 28.9, 30.8, 30.9, 30.9, 31.1, 31.1, 31.2, 31.3, 33.4, 33.4, 34.0, 34.2, 34.2, 36.9, 55.9, 63.9, 71.4, 72.8, 73.6, 73.8, 76.4, 79.7, 79.8, 106.9, 130.7, 131.2, 131.9, 132.4, 133.3, 133.4, 176.9. |
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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£º¹²²éµ½102¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 1 ÏàËÆ¶È:63.1% Journal of the Indian Chemical Society 2002 79 843-845 Nitrogenous glycerolipids from Ulva fasciate(Ulvaceae,Chlorophyta)of Eest Coast of India A.K.Siddhanta,A.M.Goswami,B.K.Ramavat and B.Achari Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1-O-¦Â-D-glucopyranosyl-(2S,3R,4E,8E)-2-[(2-hydroxyicosanoyl)amido]-4,8-octadecadiene-1,3-diol ÏàËÆ¶È:62.1% Journal of Natural Products 1996 59 319-322 New Bioactive Cerebrosides from Arisaema amurense Jee H. Jung, Chong-Ock Lee, Young Choong Kim, Sam Sik Kang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . iGb3 ÏàËÆ¶È:61.5% Bioorganic & Medicinal Chemistry Letters 2006 16 2195-2199 Synthesis and biological evaluation of ¦Á-galactosylceramide (KRN7000) and isoglobotrihexosylceramide (iGb3) Chengfeng Xia, Qingjia Yao, Jens Sch¨¹mann, Emmanuel Rossy, Wenlan Chen, Lizhi Zhu, Wenpeng Zhang, Gennaro De Libero, Peng George Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . termitomycesphin I C43H79NO10 ÏàËÆ¶È:60.5% Bioscience, Biotechnology, and Biochemistry 2012 76 1407-1409 Novel Cerebroside, Termitomycesphin I, from the Mushroom, Termitomyces titanicus Jae-Hoon CHOI, Kohei MAEDA, Hirofumi HIRAI, Etsuko HARADA, Mitsuo KAWADE, Jianhua QI, Makoto OJIKA, Hirokazu KAWAGISHI Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 1-O-¦Â-D-glucopyranosyl-(2S,3R,4E,8Z)-2-[(2(R)-hydroxyicosanoyl)amido]-4,8-octadecadiene-1,3-diol ÏàËÆ¶È:57.8% Journal of Natural Products 1996 59 319-322 New Bioactive Cerebrosides from Arisaema amurense Jee H. Jung, Chong-Ock Lee, Young Choong Kim, Sam Sik Kang Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . crispin A C40H75NO9 ÏàËÆ¶È:57.5% Chemistry & Biodiversity 2007 Vol. 4 917 Two New Protease-Inhibiting Glycosphingolipids from Buddleja crispa Ijaz Ahmad, Itrat Anis, Itrat Fatima, Abdul Malik, Shafiullah Khan, Nighat Afza, Rasool Bakhsh Tareen, Muhammad Arif Lodhi, and M. Iqbal Choudhary Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1-(n-Hexadec-7-enoxy)-6-(n-octadecanoxy)-¦Â-D-glucopyranoside C40H74O8 ÏàËÆ¶È:57.5% Chemistry of Natural Compounds 2007 43 417-421 NEW GLYCOSIDIC AND OTHER CONSTITUENTS FROM HULLS OF Oryza sativa I. M. Chung, H. Y. Park, S. C. Chun,J. J. Kim, and A. Ahmad* Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Octahydroroimatacene C30H60O7 ÏàËÆ¶È:57.5% Chemistry-A European Journal 2011 17 7875-7881 Roimatacene: An Antibiotic against Gram-Negative Bacteria Isolated from Cystobacter ferrugineus Cb G35 (Myxobacteria) Wiebke Zander, Dr. Klaus Gerth, Dr. Kathrin I. Mohr, Dipl.-Ing. Wolfgang Kessler, Dr. Rolf Jansen and Prof. Dr. Rolf M¨¹ller Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . p-Bromoacetophenone-octahydroroimatacene ester C38H65BrO8 ÏàËÆ¶È:57.1% Chemistry-A European Journal 2011 17 7875-7881 Roimatacene: An Antibiotic against Gram-Negative Bacteria Isolated from Cystobacter ferrugineus Cb G35 (Myxobacteria) Wiebke Zander, Dr. Klaus Gerth, Dr. Kathrin I. Mohr, Dipl.-Ing. Wolfgang Kessler, Dr. Rolf Jansen and Prof. Dr. Rolf M¨¹ller Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . N-{[p-(3,7-dimethyl-6R,7-dihydroxy-4R-9'''(E)-octadecenoyloxy-2-octenyloxy)phenyl]ethyl} benzamide C43H65NO6 ÏàËÆ¶È:56.7% Planta Medica 2009 75 1146-1151 New Benzamide Derivatives and NO Production Inhibitory Compounds from Limonia acidissima Ki Hyun Kim, Il Kyun Lee, Kyung Ran Kim, Sang Keun Ha, Sun Yeou Kim, Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . haliclonacyclamine A bismethiodide C33H58N2 ÏàËÆ¶È:56.7% Tetrahedron 1996 52 9111-9120 Haliclonacyclamines A and B, cytotoxic alkaloids from the tropical marine sponge Haliclona sp Romila D. Charan, Mary J. Garson, Ian M. Brereton, Anthony C. Willis, John N.A. Hooper Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . haliclonacyclamine B bismethiodide ÏàËÆ¶È:56.7% Tetrahedron 1998 54 8811-8826 The haliclonacyclamines, cytotoxic tertiary alkaloids from the tropical marine sponge Haliclona sp Richard J. Clark, Kim L. Field, Romila D. Charan, Mary J. Garson, M. Brereton, Anthony C. Willis Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-06-04 09:50:33
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