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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ
2Â¥2013-10-31 17:55:24
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