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meitianyxs

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[求助] 维普求助!M-42 已有1人参与

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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【答案】应助回帖

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感谢参与,应助指数 +1
meitianyxs: 金币+20, ★★★很有帮助 2014-09-02 19:36:58
查询模式:模糊查询
碳谱数据输入:
按从小到大顺序输入,数字间用英文半角逗号(,)分隔例如:
21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

溶剂选项:
匹配容差: (数字格式,可自行设定)
相似度:   %(相似度>=50%)



查询结果:共查到581个化合物(查询结果仅供参考)
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   碳谱模拟图
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   碳谱模拟图
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   碳谱模拟图
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   碳谱模拟图
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   碳谱模拟图
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   碳谱模拟图
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   碳谱模拟图
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   碳谱模拟图
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   碳谱模拟图
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   碳谱模拟图
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   碳谱模拟图
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   碳谱模拟图
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   碳谱模拟图
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   碳谱模拟图
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   碳谱模拟图
Domyallbesttohaveahappylife.
2楼2014-09-02 19:08:40
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meitianyxs

木虫 (正式写手)

引用回帖:
2楼: Originally posted by wangkaibo123 at 2014-09-02 19:08:40
查询模式:模糊查询
碳谱数据输入:
按从小到大顺序输入,数字间用英文半角逗号(,)分隔例如:
21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

溶剂选项:
匹配容差: (数字格式,可自行设定)
相似 ...

3楼2014-09-02 19:37:05
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