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thb237

银虫 (初入文坛)

[求助] 求助一化合物 已有2人参与

14.1, 14.2, 21.1, 22.2, 22.3, 22.6, 22.9, 26.0, 26.5, 29.7, 42.2, 45.1, 51.6, 53.0, 55.9, 60.4, 73.9, 82.8, 94.1, 101.3, 105.2, 108.4, 110.3, 116.6, 160.3, 162.2, 168.6, 191.1, 191.9, 200.4, 204.1
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lcxiong6

木虫 (小有名气)

【答案】应助回帖

★ ★ ★ ★ ★ ★
感谢参与,应助指数 +1
thb237: 金币+6, ★★★很有帮助 2015-05-25 15:34:28
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
14.1, 14.2, 21.1, 22.2, 22.3, 22.6, 22.9, 26.0, 26.5, 29.7, 42.2, 45.1, 51.6, 53.0, 55.9, 60.4, 73.9, 82.8, 94.1, 101.3, 105.2, 108.4, 110.3, 116.6, 160.3, 162.2, 168.6, 191.1, 191.9, 200.4, 204.1  
溶剂选项: 全部 CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O CD3COOD C4D8O2 D2O CF3COOD CD3OD CD3COCD3 C6D6 CD3CN 查询空值  
匹配容差: (数字格式,可自行设定)
相似度:  %(相似度>=50%)  
碳谱库:  Nat Syn



查询结果:共查到19个化合物(查询结果仅供参考)  
--------------------------------------------------------------------------------

1 .     dichrostachine L
C36H40O8     相似度:64.5%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

2 .     macrocarpal I
C28H40O6     相似度:64.5%
Journal of Natural Products          1996          59          823-827
Macrocarpals H, I, and J from the Leaves of Eucalyptus globulus
Kenji Osawa and Hideyuki Yasuda, Hiroshi Morita, Koichi Takeya, and Hideji Itokawa
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

3 .     (5'S)-17β-(1-Acetyl-5-p-fluorophenyl-3-pyrazolinyl)androst-5-en-3β-yl acetate
    相似度:64.5%
Steroids          2012          77          566-574
Synthesis of D-ring-substituted (5'R)- and (5'S)-17β-pyrazolinylandrostene epimers and comparison of their potential anticancer activities
Zoltán Iványi,Nikoletta Szabó,Judit Huber,János Wölfling,István Zupkó,Mihály Szécsi,Tibor Wittmann,Gyula Schneider
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

4 .     (5'R)-17β-(1-Acetyl-5-p-cyanophenyl-3-pyrazolinyl)androst-5-en-3β-yl acetate
C33H41N3O3     相似度:64.5%
Steroids          2012          77          566-574
Synthesis of D-ring-substituted (5'R)- and (5'S)-17β-pyrazolinylandrostene epimers and comparison of their potential anticancer activities
Zoltán Iványi,Nikoletta Szabó,Judit Huber,János Wölfling,István Zupkó,Mihály Szécsi,Tibor Wittmann,Gyula Schneider
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

5 .     (5'S)-17β-(1-Acetyl-5-p-cyanophenyl-3-pyrazolinyl)androst-5-en-3β-yl acetate
C33H41N3O3     相似度:64.5%
Steroids          2012          77          566-574
Synthesis of D-ring-substituted (5'R)- and (5'S)-17β-pyrazolinylandrostene epimers and comparison of their potential anticancer activities
Zoltán Iványi,Nikoletta Szabó,Judit Huber,János Wölfling,István Zupkó,Mihály Szécsi,Tibor Wittmann,Gyula Schneider
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

6 .     dichrostachine B
C36H40O9     相似度:63.8%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

7 .     elaphogayanin B
C32H44O8     相似度:62.5%
Journal of Natural Products          2010          73          901-904
Phloroglucinols from the Argentine Ferns Elaphoglossum gayanum and E. piloselloides
Cecilia Socolsky, Susana A. Borkosky, Marcela Hernández de Terán, Yoshinori Asakawa and Alicia Bardán
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

8 .     xylocarpin F
C31H38O11     相似度:61.2%
Journal of Natural Products          2007          70          772-778
Xylocarpins A-I, Limonoids from the Chinese Mangrove Plant Xylocarpus granatum
Jianxin Cui,Jun Wu,Zhiwei Deng, Peter Proksch,and Wenhan Lin
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

9 .     macrocarpal J
C28H40O6     相似度:61.2%
Journal of Natural Products          1996          59          823-827
Macrocarpals H, I, and J from the Leaves of Eucalyptus globulus
Kenji Osawa and Hideyuki Yasuda, Hiroshi Morita, Koichi Takeya, and Hideji Itokawa
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

10 .     compound 4
    相似度:61.2%
Chemistry of Natural Compounds          2001          37          343-346
13C NMR SPECTRA OF 5- AND 7-BROMO-6-KETOSTEROIDS AND RELATED COMPOUNDS
N. V. Kovganko, S. N. Sokolov, and V. L. Survilo
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

11 .     elaphogayanin A
C30H40O8     相似度:61.2%
Journal of Natural Products          2010          73          901-904
Phloroglucinols from the Argentine Ferns Elaphoglossum gayanum and E. piloselloides
Cecilia Socolsky, Susana A. Borkosky, Marcela Hernández de Terán, Yoshinori Asakawa and Alicia Bardán
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

12 .     7β-acetoxi-20R-hidroxi-5β,6β-epoxi-1,4-dioxo-vita-2,24-dienolido
    相似度:61.2%
Química Nova          2011          34          237-241
Cytotoxic derivatives of withanolides isolated from the leaves of Acnistus arborescens
Minguzzi, Sandro; Barata, Lauro E. S.; Cordell, Geoffrey A.
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

13 .     (3α,5α,6β,22R,4'S,5'S)-22-Acetoxy-3,5-cyclo-6-methoxy-22-(3'-methyl-4'-methoxycarbonyl-isoxazolin-5'-yl)-23,24-dinorcholane
C31H47O6N     相似度:61.2%
Steroids          2013          78          823-831
Regio- and stereocontrolled synthesis of novel steroidal isoxazolines: A new route to the formation of selectively modified steroid side chains
Halina Zhylitskaya, Raisa Litvinovskaya, Alexander Baranovsky, Václav Eigner, Bohumil Kratochvíl, Pavel Drašar, Vladimir Khripach
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

14 .     (5'R)-17β-(1'-acetyl-5'-phenyl-1H-pyrazolin-3'-yl)-5α-androstan-3β-yl acetate
C32H44N2O3     相似度:61.2%
Steroids          2014          87          86-92
Synthesis of steroidal derivatives containing substituted, fused and spiro pyrazolines
Anabel Romero-López, Sara Montiel-Smith, Socorro Meza-Reyes, Penélope Merino-Montiel, José Luis Vega-Baez
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

15 .     rhodomyrtal B
C28H40O6     相似度:61.2%
RSC Advances          2014          4          13514-13517
Rhodomyrtals A–D, four unusual phloroglucinolsesquiterpene adducts from Rhodomyrtus psidioides
Qingyao Shou, Joshua E. Smith, Htwe Mon, Zlatko Brkljača, Ana-Sunčana Smith, David M. Smith, Hans J. Griesser and Hans Wohlmuth
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

16 .     dichrostachine C
C36H40O8     相似度:61.1%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

17 .     dichrostachine E
C36H40O10     相似度:61.1%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

18 .     dichrostachine F
C36H44O9     相似度:61.1%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

19 .     dichrostachine H
C36H40O9     相似度:61.1%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------


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3楼2015-05-25 11:02:23
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seuseasoar

至尊木虫 (知名作家)

【答案】应助回帖

★ ★ ★ ★
感谢参与,应助指数 +1
thb237: 金币+4, ★★★很有帮助 2015-05-25 15:34:39
1 .     englobal-In-2
C28H38O5     相似度:54.8%
Natural Medicines          1997          51          486-490
Euglobals-In 2 and -In-3, New Euglobals from Eucalyptus incrassata
TAKASAKI MIDORI,KONOSHIMA TAKAO,KOZUKA MUTSUO,HARUNA MITSUMASA,ITO KAZUO
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图
2 .     dichrostachine H
C36H40O9     相似度:52.7%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图
3 .     dichrostachine L
C36H40O8     相似度:51.6%
Journal of Natural Products          2009          72          1804-1815
Meroterpenes from Dichrostachys cinerea Inhibit Protein Farnesyl Transferase Activity
Christophe Long, Laurence Marcourt, Roselyne Raux, Bruno David, Christelle Gau, Christophe Menendez,Min Gao,Marie-France Laroche, Philippe Schambel, Clement Delaude, Frederic Ausseil, Catherine Lavaud, and Georges Massiot
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图
4 .     4-Acetoxy-plakinamine B
C33H52N2O2     相似度:51.5%
Steroids          2007          72          682-685
Acetylcholinesterase-inhibiting steroidal alkaloid from the sponge Corticium sp.
Roosanee Langjae, Somchai Bussarawit, Supreeya Yuenyongsawad, Kornkanok Ingkaninan, Anuchit Plubrukarn
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图
尼赫
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