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ÇÑ×Ó¼ÓÓÍ: ½ð±Ò+20, ¡ïÓаïÖú 2013-04-18 15:04:10
1 .     6-hydroxy-4',7-dimethoxyisoflavone
C17H14O5     ÏàËÆ¶È:81.2%
Chemical & Pharmaceutical Bulletin          2009          57          346-360
Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities
Hideyuki Goto, Yoshiyasu Terao and Shuji Akai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     4',6-dimethoxy-7-hydroxyisoflavone
    ÏàËÆ¶È:75%
Chemistry of Natural Compounds          2009          45          420-421
ISOLATION AND IDENTIFICATION OF 4¡ä,6-DIMETHOXY-7-HYDROXYISOFLAVONEFROM ROOTS OF Hedysarum theinum CULTIVATED in vitro
I. V. Nechepurenko, N. I. Komarova, I. N. Kuzovkina,M. Yu. Vdovitchenko, M. P. Polovinka,and N. F. Salakhutdinov1
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     glycitrin
    ÏàËÆ¶È:75%
China Journal of Chinese Materia Medica          2003          28          43-47
Isolation and Elucidation of Chemical Constituents with Antiviral Action from Yinqiaosan on Influenza Virus
SHI Yue, SHI Renbing, LIU Bin, LU Yunru, DU Lijun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     7-hydroxy-6,4'-dimethoxyisoflavone
    ÏàËÆ¶È:75%
Phytochemistry          1998          47          117-119
Isoflavonoids and a pterocarpan from Gliricidia sepium
H. M. T. B. Herath, R. S. Dassanayake, A. M. A. Priyadarshani, Susila De Silva, G. P. Wannigama, Joanne Jamie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     7-hydroxy-4',6-dimethoxyisoflavone
C17H14O5     ÏàËÆ¶È:75%
Chemical & Pharmaceutical Bulletin          2009          57          346-360
Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities
Hideyuki Goto, Yoshiyasu Terao and Shuji Akai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     formonoetin
    ÏàËÆ¶È:75%
Fitoterapia          2010          81          1058-1061
New isoflavonolignan with quinone reductase inducing activity from Alhagi pseudalhagi (M.B.)
Ning Li, Guijie Zhang, Yuanjun Xiong, Bolat Makhabel, Xian Li, Xiaoguang Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     afrormosin
    ÏàËÆ¶È:75%
Chinese Journal of Natural Medicines          2006          4          151-153
The Anticancer Activity in vitro of Constituents from Fruits of Sophora japonica
MA Lei; LOU Feng-Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 3
    ÏàËÆ¶È:75%
Archives of Pharmacal Research          1991          14          105-108
Insecticidal isoflavon glycoside from Maackia amurensis
Hasik Youn, Sangkyun Lee, Jin-Ho Cho and Hunseung Oh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     formononetin
    ÏàËÆ¶È:75%
Chinese Pharmaceutical Journal          2005          40          1057-1059
Studies on chemical constituents of Trifolium pratense
MA Qiang, LEI Hai-min, ZHOU Yu-xin, WANG Chang-hai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     formononetin
    ÏàËÆ¶È:75%
Chinese Pharmaceutical Journal          2006          41          1217-1221
Studies on Chemical Constituents of Astragalus membranaceus(Fisch.) Bge.var.mongholicus(Bge.) Hsiao
BIAN Yun-yun, GUAN Jia, BI Zhi-ming, SONG Yue, LI Ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     afromosin
    ÏàËÆ¶È:75%
Chinese Pharmaceutical Journal          2009          44          1533-1535
Isoflavonoids from Hedysarum semenovii
LIU Yi, HAI Li-qian, ZHAO Yu-ying, ZHANG Qing-ying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     afromosin
C17H14O5     ÏàËÆ¶È:75%
Food Chemistry          2011          126          1057-1063
The most abundant polyphenol of soy leaves, coumestrol, displays potent ¦Á-glucosidase inhibitory activity
Heung Joo Yuk, Jin Hwan Lee, Marcus J. Curtis-Long, Ji Won Lee, Young Soo Kim, Hyung Won Ryu, Chung Gyoo Park, Tae-Sook Jeong, Ki Hun Park
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     formononetin
    ÏàËÆ¶È:75%
Journal of Agricultural and Food Chemistry          2006          54          2057-2063
LDL-Antioxidant Pterocarpans from Roots of Glycine max (L.) Merr.
Jin Hwan Lee, Byong Won Lee, Jin Hyo Kim, Tae-Sook Jeong, Min Jung Kim, Woo Song Lee, and Ki Hun Park
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     Formononetin
C16H12O4     ÏàËÆ¶È:75%
Journal of Chinese Pharmaceutical Sciences          2012          21          428-434
Chemical constituents of Pseudolarix kaempferi Gord
Tianzhi Cai; Wen Qi; Lianmei Yang; Guangzhong Tu; Rong Yang; Kehui Xie; Hongzheng Fu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     afrormosin
C17H14O5     ÏàËÆ¶È:70.5%
Chinese Pharmaceutical Journal          2006          41          1217-1221
Studies on Chemical Constituents of Astragalus membranaceus(Fisch.) Bge.var.mongholicus(Bge.) Hsiao
BIAN Yun-yun, GUAN Jia, BI Zhi-ming, SONG Yue, LI Ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     8-O-methylretusin
    ÏàËÆ¶È:70.5%
International Journal of Molecular Sciences          2012          13          11349-11364
Phenolic Compounds from Halimodendron halodendron (Pall.) Voss and Their Antimicrobial and Antioxidant Activities
Jihua Wang, Jingfeng Lou, Chao Luo, Ligang Zhou, Mingan Wang and Lan Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     formononetin
    ÏàËÆ¶È:68.7%
Planta Medica          1988          54          250-254
Isolation and High Performance Liquid Chromatography (HPLC) of Isoflavonoids from the Pueraria Root
Yukio Ohshima, Toru Okuyama, Kunio Takahashi, Toshio Takizawa, and Shoji Shibata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     7-Hydroxyl-4'-methoxyisoflavone
C16H12O4     ÏàËÆ¶È:68.7%
Chemistry of Natural Compounds          2007          43          214-215
CHEMICAL RESEARCH OF Caragana microphylla Seeds
Yan Huo, Cheng Guo, Shan Lu,Qiao-Yan Zhang, and Lu-Ping Qin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     Formononetin
    ÏàËÆ¶È:68.7%
Chemistry of Natural Compounds          2007          43          614-615
FLAVONOIDS FROM Trifolium resupinatum VAR. microcephalum
Emel Isik, Temine Sabudak, and Sevi Oksuz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     Formononetin
C16H12O4     ÏàËÆ¶È:68.7%
Chemistry of Natural Compounds          2002          38          473-519
PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES
V. M. Malikov and M. P. Yuldashev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     Formononetin
    ÏàËÆ¶È:68.7%
Journal of Chinese Pharmaceutical Sciences          2006          15          15-20
Flavanoids from Clematis hexapetala
DONG Cai-xia; WU Ke-si; SHI She-po; and TU Peng-fei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     formononetin
    ÏàËÆ¶È:68.7%
China Journal of Chinese Materia Medica          2003          28          43-53
Isolation and Elucidation of Chemical Constituents with Antiviral Action from Yinqiaosan on Influenza Virus
SHI Yue, SHI Renbing, LIU Bin, LU Yunru, DU Lijun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     formononetin
    ÏàËÆ¶È:68.7%
Acta Pharmaceutica Sinica          2003          Vol 38          592-595
Studies on chemical constituents of Hedysarum polybotrys
HAI Li qian; ZHANG Qing ying; LIANG Hong; ZHAO Yu ying; DU Nian sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     Herbacetin 4'-methyl ether
C16H12O7     ÏàËÆ¶È:68.7%
Phytochemistry          1994          37          455-456
A herbacetin methyl ether from the farinose exudate of a Pentagramma triangularis hybrid
Eckhard Wollenweber, Sylvia Armbruster, James N. Roitman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     4',6-dihydroxy-7-methoxyisoflavone
C16H12O5     ÏàËÆ¶È:68.7%
Chemical & Pharmaceutical Bulletin          2009          57          346-360
Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities
Hideyuki Goto, Yoshiyasu Terao and Shuji Akai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     8-hydroxy-4'-methoxy-7-methylisoflavone
C17H14O4     ÏàËÆ¶È:68.7%
Chemical & Pharmaceutical Bulletin          2009          57          346-360
Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities
Hideyuki Goto, Yoshiyasu Terao and Shuji Akai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     4',6,7-trimethoxyisoflavone
C18H16O5     ÏàËÆ¶È:68.7%
Chemical & Pharmaceutical Bulletin          2009          57          346-360
Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities
Hideyuki Goto, Yoshiyasu Terao and Shuji Akai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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