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meitianyxs木蟲 (正式寫手)
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維普求助,謝謝。! 已有1人參與
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| 13C NMR (101 MHz, Pyr) δ: 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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查詢模式:模糊查詢 碳譜數(shù)據(jù)輸入: 按從小到大順序輸入,數(shù)字間用英文半角逗號(hào)(,)分隔例如: 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 溶劑選項(xiàng): 匹配容差: (數(shù)字格式,可自行設(shè)定) 相似度: %(相似度>=50%) 查詢結(jié)果:共查到102個(gè)化合物(查詢結(jié)果僅供參考) 1 . compound 1 相似度: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 碳譜模擬圖 2 . 1-O-β-D-glucopyranosyl-(2S,3R,4E,8E)-2-[(2-hydroxyicosanoyl)amido]-4,8-octadecadiene-1,3-diol 相似度: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 碳譜模擬圖 3 . iGb3 相似度:61.5% Bioorganic & Medicinal Chemistry Letters 2006 16 2195-2199 Synthesis and biological evaluation of α-galactosylceramide (KRN7000) and isoglobotrihexosylceramide (iGb3) Chengfeng Xia, Qingjia Yao, Jens Schümann, Emmanuel Rossy, Wenlan Chen, Lizhi Zhu, Wenpeng Zhang, Gennaro De Libero, Peng George Wang Structure 13C NMR 碳譜模擬圖 4 . termitomycesphin I C43H79NO10 相似度: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 碳譜模擬圖 5 . 1-O-β-D-glucopyranosyl-(2S,3R,4E,8Z)-2-[(2(R)-hydroxyicosanoyl)amido]-4,8-octadecadiene-1,3-diol 相似度: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 碳譜模擬圖 6 . crispin A C40H75NO9 相似度: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 碳譜模擬圖 7 . 1-(n-Hexadec-7-enoxy)-6-(n-octadecanoxy)-β-D-glucopyranoside C40H74O8 相似度: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 碳譜模擬圖 8 . Octahydroroimatacene C30H60O7 相似度: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 Müller Structure 13C NMR 碳譜模擬圖 9 . p-Bromoacetophenone-octahydroroimatacene ester C38H65BrO8 相似度: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 Müller Structure 13C NMR 碳譜模擬圖 10 . N-{[p-(3,7-dimethyl-6R,7-dihydroxy-4R-9'''(E)-octadecenoyloxy-2-octenyloxy)phenyl]ethyl} benzamide C43H65NO6 相似度: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 碳譜模擬圖 11 . haliclonacyclamine A bismethiodide C33H58N2 相似度: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 碳譜模擬圖 12 . haliclonacyclamine B bismethiodide 相似度: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 碳譜模擬圖 |

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