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meitianyxs木蟲(chóng) (正式寫(xiě)手)
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[求助]
維普求助！M-42 已有1人參與
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| 13C NMR (101 MHz, MeOD) δ: 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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wangkaibo123
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kerry
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專(zhuān)家經(jīng)驗(yàn): +726 - PhEPI: 3
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【答案】應(yīng)助回帖
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感謝參與，應(yīng)助指數(shù) +1
meitianyxs: 金幣+20, ★★★很有幫助 2014-09-02 19:36:58
感謝參與，應(yīng)助指數(shù) +1
meitianyxs: 金幣+20, ★★★很有幫助 2014-09-02 19:36:58
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查詢(xún)模式：模糊查詢(xún) 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(xún)結(jié)果：共查到581個(gè)化合物(查詢(xún)結(jié)果僅供參考) 1 . (2S,3R,4E,8E,2'R-)-1-O-(β-D-Glucopyranosyl)-N-(2'-hydroxyhexadecanoyl)-4,8-sphinyadienine 相似度: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 碳譜模擬圖 2 . (2S,3R,4E,8 Z,2'R)-1-O-(β-D-Glucopyranosyl)-N-(2'-hydrox yhexadecanoyl)-4,8-sphingadienin 相似度: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 碳譜模擬圖 3 . triumfettoside Ic C42H73NO9 相似度: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 碳譜模擬圖 4 . magnolioside 相似度:78.1% Bulletin of the Academy of Military Medical Sciences 2013 37 279-282 Chemical constituents from Solanum lyratum Thunb. ( Ⅱ) YIN Hai-long, LI Jian, DONG Jun-xing Structure 13C NMR 碳譜模擬圖 5 . 1-O-β-D-glucopyranosyl-(2S,3R,4E,8Z)-2-N-palmitoyloctadecasphinga-4,8-dienine C40H75NO8 相似度: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 碳譜模擬圖 6 . 1-O-β-D-glucopyranosyl-(2S,3S,4R,8E)-2-[(2'R)-2'-hydroxypalmitoyl amino]-8-octadecene-1,3,4-triol 相似度: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 碳譜模擬圖 7 . 1-O-β-D-glucopyranosyl(2S,3S,4R,8E)-2-[(2'R)-2'-hydroxytetra cosanamino]-8-octadecene-1,3,4-triol 相似度: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 碳譜模擬圖 8 . 1-O-β-D-glucopyranosyl-(2S,3S,4R,8E)-2-[(2'R)-2'-hydroxy-tetracosanoyl]-8-octadecene-1,3,4-triol C48H93NO10 相似度: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 碳譜模擬圖 9 . compound 4 C36H66O9 相似度: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 碳譜模擬圖 10 . Ophidiacerebroside C C47H87NO9 相似度: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 碳譜模擬圖 11 . alternaroside C C42H77NO9 相似度: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 碳譜模擬圖 12 . Chrysogeside A C40H73NO9 相似度: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 碳譜模擬圖 13 . Buteagibrenol Glycoside C27H48O11 相似度: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 碳譜模擬圖 14 . (2S,2'R,3R,3'E,4E,8E,10E)-1-O-β-D-glucopyranosyl-2-N-(2'-hydroxy-3'-octadecenoyl)-3-hydroxy-9-methyl-4,8,10-sphingatrienine C43H77NO9 相似度: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 碳譜模擬圖 15 . Ophidiacerebroside E C49H89NO9 相似度: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 碳譜模擬圖 |
2樓2014-09-02 19:08:40
meitianyxs
木蟲(chóng) (正式寫(xiě)手)
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3樓2014-09-02 19:37:05
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