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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 CDCl3 |
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thb237: ½ð±Ò+4, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-25 15:34:39
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thb237: ½ð±Ò+4, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-25 15:34:39
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1 . englobal-In-2 C28H38O5 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ 2 . dichrostachine H C36H40O9 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ 3 . dichrostachine L C36H40O8 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ 4 . 4-Acetoxy-plakinamine B C33H52N2O2 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ |

2Â¥2015-05-25 11:00:10
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thb237: ½ð±Ò+6, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-25 15:34:28
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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 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 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O CD3COOD C4D8O2 D2O CF3COOD CD3OD CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ̼Æ×¿â£º Nat Syn ²éѯ½á¹û£º¹²²éµ½19¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . dichrostachine L C36H40O8 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . macrocarpal I C28H40O6 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (5'S)-17¦Â-(1-Acetyl-5-p-fluorophenyl-3-pyrazolinyl)androst-5-en-3¦Â-yl acetate ÏàËÆ¶È:64.5% Steroids 2012 77 566-574 Synthesis of D-ring-substituted (5'R)- and (5'S)-17¦Â-pyrazolinylandrostene epimers and comparison of their potential anticancer activities Zolt¨¢n Iv¨¢nyi,Nikoletta Szab¨®,Judit Huber,J¨¢nos Wölfling,Istv¨¢n Zupk¨®,Mih¨¢ly Sz¨¦csi,Tibor Wittmann,Gyula Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (5'R)-17¦Â-(1-Acetyl-5-p-cyanophenyl-3-pyrazolinyl)androst-5-en-3¦Â-yl acetate C33H41N3O3 ÏàËÆ¶È:64.5% Steroids 2012 77 566-574 Synthesis of D-ring-substituted (5'R)- and (5'S)-17¦Â-pyrazolinylandrostene epimers and comparison of their potential anticancer activities Zolt¨¢n Iv¨¢nyi,Nikoletta Szab¨®,Judit Huber,J¨¢nos Wölfling,Istv¨¢n Zupk¨®,Mih¨¢ly Sz¨¦csi,Tibor Wittmann,Gyula Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (5'S)-17¦Â-(1-Acetyl-5-p-cyanophenyl-3-pyrazolinyl)androst-5-en-3¦Â-yl acetate C33H41N3O3 ÏàËÆ¶È:64.5% Steroids 2012 77 566-574 Synthesis of D-ring-substituted (5'R)- and (5'S)-17¦Â-pyrazolinylandrostene epimers and comparison of their potential anticancer activities Zolt¨¢n Iv¨¢nyi,Nikoletta Szab¨®,Judit Huber,J¨¢nos Wölfling,Istv¨¢n Zupk¨®,Mih¨¢ly Sz¨¦csi,Tibor Wittmann,Gyula Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . dichrostachine B C36H40O9 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . elaphogayanin B C32H44O8 ÏàËÆ¶È: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 Hern¨¢ndez de Ter¨¢n, Yoshinori Asakawa and Alicia Bard¨¢n Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . xylocarpin F C31H38O11 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . macrocarpal J C28H40O6 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . compound 4 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . elaphogayanin A C30H40O8 ÏàËÆ¶È: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 Hern¨¢ndez de Ter¨¢n, Yoshinori Asakawa and Alicia Bard¨¢n Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 7¦Â-acetoxi-20R-hidroxi-5¦Â,6¦Â-epoxi-1,4-dioxo-vita-2,24-dienolido ÏàËÆ¶È:61.2% Qu¨ªmica 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (3¦Á,5¦Á,6¦Â,22R,4'S,5'S)-22-Acetoxy-3,5-cyclo-6-methoxy-22-(3'-methyl-4'-methoxycarbonyl-isoxazolin-5'-yl)-23,24-dinorcholane C31H47O6N ÏàËÆ¶È: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, V¨¢clav Eigner, Bohumil Kratochv¨ªl, Pavel Drašar, Vladimir Khripach Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (5'R)-17¦Â-(1'-acetyl-5'-phenyl-1H-pyrazolin-3'-yl)-5¦Á-androstan-3¦Â-yl acetate C32H44N2O3 ÏàËÆ¶È:61.2% Steroids 2014 87 86-92 Synthesis of steroidal derivatives containing substituted, fused and spiro pyrazolines Anabel Romero-L¨®pez, Sara Montiel-Smith, Socorro Meza-Reyes, Pen¨¦lope Merino-Montiel, Jos¨¦ Luis Vega-Baez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . rhodomyrtal B C28H40O6 ÏàËÆ¶È:61.2% RSC Advances 2014 4 13514-13517 Rhodomyrtals A¨CD, 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . dichrostachine C C36H40O8 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . dichrostachine E C36H40O10 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . dichrostachine F C36H44O9 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . dichrostachine H C36H40O9 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- Copyright © 2009-2011 ÉϺ£Î¢Æ×ÐÅÏ¢¼¼ÊõÓÐÏÞ¹«Ë¾ Shanghai Micronmr Infor Technology Co., Ltd., All Rights Reserved µØÖ·£ºÉϺ£ÊÐÑîÆÖÇøºªµ¦Â·100ºÅ61¶°131ÊÒ(¸´µ©¿Æ¼¼Ô°), Óʱà:200437 E-mail: micronmr@126.com ×Éѯµç»°:086-021-61736083 »¦ICP±¸10026489ºÅ |
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