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º£ÀËÖðÃÎ: ½ð±Ò+5, ¡ïÓаïÖú 2013-10-31 19:55:18
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²éѯ½á¹û£º¹²²éµ½67¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . neochamaejasmin B ÏàËÆ¶È:68% Chemistry of Natural Compounds 2009 45 542-544 FLAVONOIDS FROM Daphne holosericea Yuqi Chen Juan Su, Yunheng Shen,Wei Zhang, Shuang Liang,Weidong Zhang,and Lingyi Kong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compound 7 ÏàËÆ¶È:65.3% Phytochemistry 1994 35 1567-1572 Isoflavanone dimers hexaspermone A, B and C from Ouratea hexasperma Isabel Craveiro Moreira, Dari C. Sobrinho, Mario Geraldo De Carvalho, Raimundo Braz-Filho Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 4-{[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl]oxy} butanoic acid C19H18O7 ÏàËÆ¶È:63.6% Food Chemistry 2010 118 472-481 Development and validation of two new sensitive ELISAs for Hesperetin and Naringenin in biological fluids Svitlana Shinkaruk, Val¨¦rie Lamothe, Jean-Marie Schmitter, Claudine Manach, Christine Morand, Annie Berard, Bernard Bennetau, Catherine Bennetau-Pelissero Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . mesuaferrone B ÏàËÆ¶È:62.5% Journal of Ethnopharmacology 2012 142 213-220 Rhus parviflora and its biflavonoid constituent,rhusflavone,inducesleep through the positive allosteric modulation of GABAA benzodiazepine receptors Sabina Shrestha, Ji-HaePark, Dae-YoungLee, Jin-GyeongCho, SuengmokCho, Hye-JinYang, Hye-Im Yong, Min-SeokYoon, Dae-SeokHan, Nam-InBaek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . compound 6 ÏàËÆ¶È:61.5% Phytochemistry 1994 35 1567-1572 Isoflavanone dimers hexaspermone A, B and C from Ouratea hexasperma Isabel Craveiro Moreira, Dari C. Sobrinho, Mario Geraldo De Carvalho, Raimundo Braz-Filho Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Apigeninyl-(I-3,II-3)-naringenin C30H20O10 ÏàËÆ¶È:61.5% Phytochemistry 2010 71 785-791 Antiplasmodial activity of (I-3,II-3)-biflavonoids and other constituents from Ormocarpum kirkii Liene Dhooghe, Sheila Maregesi, Irena Mincheva, Daneel Ferreira, Jannie P.J. Marais, Filip Lemi¨¨re, An Matheeussen, Paul Cos, Louis Maes, Arnold Vlietinck, Sandra Apers, Luc Pieters Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . rhusflavanone ÏàËÆ¶È:60% Journal of Ethnopharmacology 2012 142 213-220 Rhus parviflora and its biflavonoid constituent,rhusflavone,inducesleep through the positive allosteric modulation of GABAA benzodiazepine receptors Sabina Shrestha, Ji-HaePark, Dae-YoungLee, Jin-GyeongCho, SuengmokCho, Hye-JinYang, Hye-Im Yong, Min-SeokYoon, Dae-SeokHan, Nam-InBaek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . neochamaejasmin B ÏàËÆ¶È:60% Pharmaceutical Biology 2003 41 59-61 Biflavonoids from Stellera chamaejasme Baomin Feng, Yuehu Pei, Huiming Hua, Tao Wang, Yi Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . isosikokianin A C31H24O10 ÏàËÆ¶È:59.2% Chemistry & Biodiversity 2008 Vol. 5 1419 Biflavanones, Flavonoids, and Coumarins from the Roots of Stellera chamaejasme and Their Antiviral Effect on Hepatitis B Virus Guohong Yang and Daofeng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 6-{[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl]oxy}hexanoic acid C21H22O7 ÏàËÆ¶È:59.0% Food Chemistry 2010 118 472-481 Development and validation of two new sensitive ELISAs for Hesperetin and Naringenin in biological fluids Svitlana Shinkaruk, Val¨¦rie Lamothe, Jean-Marie Schmitter, Claudine Manach, Christine Morand, Annie Berard, Bernard Bennetau, Catherine Bennetau-Pelissero Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . naringenin-7-O-¦Á-glucoside ÏàËÆ¶È:59.0% European Food Research and Technology 2007 225 777-782 Identification of flavanones from peel of Citrus changshan-huyou Y.B.Chang, by HPLC¨CMS and NMR Chunmei Li, Haifeng Gu, Hongliang Dou, Liming Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . rhusflavone ÏàËÆ¶È:56% Journal of Ethnopharmacology 2012 142 213-220 Rhus parviflora and its biflavonoid constituent,rhusflavone,inducesleep through the positive allosteric modulation of GABAA benzodiazepine receptors Sabina Shrestha, Ji-HaePark, Dae-YoungLee, Jin-GyeongCho, SuengmokCho, Hye-JinYang, Hye-Im Yong, Min-SeokYoon, Dae-SeokHan, Nam-InBaek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 7-methoxylneochaejasmin A C31H24O10 ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 2002 50(1) 137-139 Biflavanones, Diterpenes, and Coumarins from the Roots of Stellera chamaejasme L. Zhi-Hong JIANG£¬Takashi TANAKA, Takako SAKAMOTO,Isao KOUNO,Jin-Ao DUAN,and Rong-Han ZHOU Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . phelligrin B C22H18O6 ÏàËÆ¶È:54.5% Chinese Chemical Letters 2003 14 810-813 Two Benzyl Dihydroflavones from Phellinus igniarius Shun Yan MO, Wen Yi HE, Yong Chun YANG, Jian Gong SHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 7-methoxyneochamaejasmin A ÏàËÆ¶È:54.5% Journal of Asian Natural Products Research 2002 4 259-263 CHEMICAL CONSTITUENTS OF STELLERA CHAMAEJASME L BAO-MIN FENG, YUE-HU PEI and HUI-MING HUA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 6-(1,1-dimethylullyl)naringenin C20H20O5 ÏàËÆ¶È:54.5% Phytochemistry 1997 45 509-515 Cytotoxic prenylated flavanones from Monotes engleri E. -K. Seo, G. L. Silva, H. -B. Chai, T. E. Chagwedera, N. R. Farnsworth, G. A. Cordell, J. M. Pezzuto, A. D. Kinghorn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Sikokianin C C31H24O10 ÏàËÆ¶È:54.5% Phytochemistry 1994 37 879-883 Three biflavonoids from Wikstroemia sikokiana Kimlye Baba, Masahiko Taniguchi, Mitsugi Kozawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . naringenin 7-O-¦Â-glucuronopyranoside ÏàËÆ¶È:54.5% Chemistry & Biodiversity 2012 9 2096-2158 Flavonoids in Subtribe Centaureinae (Cass.) Dumort. (Tribe Cardueae, Asteraceae): Distribution and 13C-NMR Spectral Data Carmen Formisano, Daniela Rigano, Felice Senatore, Svetlana Bancheva, Antonella Maggio, Sergio Rosselli and Maurizio Bruno Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (2S)-5-hydroxy-7,4'-di-O-(¦Ã,¦Ã-dimethylallyl)flavanone C25H28O5 ÏàËÆ¶È:54.5% Natural Product Communications 2009 4 59-62 Flavonoids from Tephrosia calophylla Ramireddy V. Narahari Reddya, Shaik I. Khalivullaa, Bandi A.K. Reddya,Mopuru V. Bhaskar Reddya,b, Duvvuru Gunasekara,, Alexandre Devillec and Bernard Bodo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . Macatrichocarpin A C21H22O5 ÏàËÆ¶È:54.5% Natural Product Communications 2009 4 63-67 Isoprenylated Flavanones and Dihydrochalcones fromMacaranga trichocarpa Yana M. Syah, Euis H. Hakim, Sjamsul A. Achmad, Muhamad Hanafi andEmilio L. Ghisalberti Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . phelligrin B C22H18O6 ÏàËÆ¶È:54.5% Acta Chimica Sinica 2003 61 1161-1163 Isoation and systhesis of phelligrins A and B MO, Shun-Yan YANG, Yong-Chen SHI Jian-Gong Structure 13C NMR ̼Æ×Ä£Äâͼ |
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