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55.27,101.73,103.19,108.63,110.50,114.26,115.99,117.97,122.94,124.66,125.42,128.29,130.87,152.84,153.07,158.60,160.00,164.21,175.69
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ferhung: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-03-26 09:07:25
.     7-methoxy-3',4'-methylenedioxyisoflavone
C17H12O5     ÏàËÆ¶È:73.6%
Journal of Natural Products          2003          66          210-216
Six New Isoflavones and a 5-Deoxyflavonol Glycoside from the Leaves of Ateleia herbert-smithii
Nigel C. Veitch, Polly S. E. Sutton, Geoffrey C. Kite, and Helen E. Ireland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     Formononetin
    ÏàËÆ¶È:73.6%
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

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3 .     formononetin
    ÏàËÆ¶È:73.6%
China Journal of Chinese Materia Medica          2003          28          527-533
Chemical Constituents from the Leaves of Dalbergia hainanensis
ZHANG Peicheng, WU Yan, YU Dequan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     Formononetin
    ÏàËÆ¶È:73.6%
Natural Product Sciences          2008          14          131-137
Phytochemical Studies on Astragalus Root (2);Flavonoids and a Lignan
Lee, Eun-Ju; Yean, Min-Hye; Jung, Hye-Sil; Kim, Ju-Sun; Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     formononetin
    ÏàËÆ¶È:73.6%
Chinese Traditional and Herbal Drugs          2010          41          696-700
Isolation and identification of flavonoids from Baoyuan Decoction
SUN Jing-wei; ZHAO Ming-bo; LIANG Hong; TU Peng-fei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     Formononetin
    ÏàËÆ¶È:68.4%
Chemistry of Natural Compounds          2006          42          567-570
NEW THIAZINEDIONES AND OTHER COMPONENTS FROM Xanthium strumarium
Ting Han, Huiliang Li, Qiaoyan Zhang,Hanchen Zheng, and Luping Qin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     formononetin
    ÏàËÆ¶È:68.4%
China Journal of Chinese Materia Medica          2004          29          434-436
Studies on chemical constituents of Sini Tang
LIU Hongxia, LIN Wenhan, YANG Junshan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     3'-¼×Ñõ»ù-4',7-¶þôÇ»ùÒì»ÆÍª(4',7-dihydroxy-3'-methoxylisoflavone)
C16H12O5     ÏàËÆ¶È:68.4%
China Journal of Chinese Materia Medica          2011          Vol 36,Issue 7          886-890
Study on chemical constituents of Picrasma quassioides
ZHU Chenchen, DENG Guihua, LIN Chaozhan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     4'-methoxy-7-hydroxyisoflavone
    ÏàËÆ¶È:68.4%
China Journal of Chinese Materia Medica          2010          35          2416-2419
Chemical constituents of bear bile
LUO Qiang; CHEN Quancheng; WU Yao; JIANG Miaomiao; CHEN Zhihong; ZHANG Xiaokun; CHEN Haifeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     formonoetin
    ÏàËÆ¶È:68.4%
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

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11 .     Ã¢±úÒì»ÆÍª
C16H12O4     ÏàËÆ¶È:68.4%
Chinese Traditional and Herbal Drugs          2009          40          865-868
Ðâëǧ½ï°Î¸ùµÄ»¯Ñ§³É·ÖÑо¿
ÕÅÑ©;ËÎÆôʾ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     Pseudobaptigenin
    ÏàËÆ¶È:68.4%
Archives of Pharmacal Research          2004          27          589-592
Flavonoids from Spatholobus suberectus
Jeong Seon Yoon, Sang Hyun Sung, Jong Hee Park and Young Choong Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     Corylin
    ÏàËÆ¶È:68.4%
Archives of Pharmacal Research          2010          33          999-1003
Neuroprotective effects of constituents of Eragrostis ferruginea against A¦Â-induced toxicity in PC12 cells
Chae Sun Na, Seong Su Hong, Yun-Hyeok Choi, Yong Ho Lee and Sun Hee Hong, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     formononetin
C16H12O4     ÏàËÆ¶È:68.4%
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

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15 .     formononetin
    ÏàËÆ¶È:68.4%
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

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16 .     Formononetin
C16H12O4     ÏàËÆ¶È:68.4%
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

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17 .     3',7-dihydroxy-4'-methoxyisoflavone
C16H12O5     ÏàËÆ¶È:68.4%
Natural Product Research and Development          2012          24          476-478
Chemical Constituents of Picrasma quassioides(D.Don) Benn.
ZHU Chen-chen; DENG Gui-hua; LIN Chao-zhan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     Ã¢±ú»¨ËØ
    ÏàËÆ¶È:68.4%
China Journal of Chinese Materia Medica          2012          37          3243-3248
Isoflavonoids from roots of Astragalus membranaceus var. mongholicus
ZHANG Ya-zhou; XU Feng; LIANG Jing; TANG Jing-shu; SHANG Ming-ying; WANG Xuan; CAI Shao-qing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     7-(2-Methylallyloxy)-3-(4-methoxy-3-nitrophenyl)-4H-chromen-4-one
    ÏàËÆ¶È:65%
European Journal of Medicinal Chemistry          2012          54          175-187
Synthesis and antitumor activity of formononetin nitrogen mustard derivatives
Jie Ren, Hua-Jin Xu, Hong Cheng, Wen-Qun Xin, Xin Chen, Kun Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     7,2'-dimethoxy-4',5'-methylenedioxyisoflavone
C18H14O6     ÏàËÆ¶È:63.1%
Journal of Natural Products          2003          66          210-216
Six New Isoflavones and a 5-Deoxyflavonol Glycoside from the Leaves of Ateleia herbert-smithii
Nigel C. Veitch, Polly S. E. Sutton, Geoffrey C. Kite, and Helen E. Ireland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     7,4'-Dimethoxyisoflavone
C17H14O4     ÏàËÆ¶È:63.1%
Journal of Natural Products          2003          66          210-216
Six New Isoflavones and a 5-Deoxyflavonol Glycoside from the Leaves of Ateleia herbert-smithii
Nigel C. Veitch, Polly S. E. Sutton, Geoffrey C. Kite, and Helen E. Ireland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     7-hydroxy-4'-methoxyisoflavone
    ÏàËÆ¶È:63.1%
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

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23 .     agrostophylloxin
C18H14O5     ÏàËÆ¶È:63.1%
Phytochemistry          1996          42          1157-1161
Four stilbenoids from the orchid Agrostophyllum khasiyanum
P. L. Majumder, S. Lahiri, N. Mukhoti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     compound 1c
    ÏàËÆ¶È:63.1%
Phytochemistry          1991          30          971-974
Isoflaccidinin and isooxoflaccidin, stilbenoids from Coelogyne flaccida
P.L. Majumder, D.C. Maiti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     formononetin:7-hydroxy-4'-methoxy-isoflavone:4H-1-benzopyran-4-one,7-hydroxy-3-(4-methoxyphenyl)
    ÏàËÆ¶È:63.1%
Korean Journal of Pharmacognosy          1997          28(2)          75-79
A Study on the Constituents from the Roots of Astragalus membranaceus (II)
Kim, Jin-Sook; Kim, Chung-Sook
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     9-Ethyl-6-hydroxy-3-(4-methoxy-phenylthio)-9H-carbazole-1,4-dione
    ÏàËÆ¶È:63.1%
Bioorganic & Medicinal Chemistry Letters          2011          21          427-430
Synthesis and antifungal evaluation of 6-hydroxy-1H-carbazole-1,4(9H)-diones
Chung-Kyu Ryu, Seung-Yon Lee, Na Young Kim, Jung An Hong, Joo Hee Yoon, Aram Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     2-Amino-4-(4-bromothenyloxy)-6-[N-(4-(4-aminophenylamino)anilino)]-5-nitropyrimidine
C21H18BrN7O3S     ÏàËÆ¶È:63.1%
Bioorganic & Medicinal Chemistry          2011          19          1658-1665
Towards more specific O6-methylguanine-DNA methyltransferase (MGMT)inactivators
Sergio Lopez, Geoffrey P. Margison, R. Stanley McElhinney, Alessandra Cordeiro,T. Brian H. McMurry, Isabel Rozas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     lycoranine A
C17H11NO4     ÏàËÆ¶È:63.1%
Chemical & Pharmaceutical Bulletin          2009          57          610-611
Two New Amaryllidaceae Alkaloids from the Bulbs of Lycoris radiata
Lei Wang, Xiao-Qi Zhang, Zhi-Qi Yin, Ying Wang and Wen-Cai Ye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     nordurlettone
C20H18O4     ÏàËÆ¶È:63.1%
Phytochemistry          1990          29          2671-2673
O-Geranylated and O-prenylated flavonoids from Millettia ferruginea
Ermias Dagne,Amha Bekele,Hi Noguchi,Masaki Shibuya,Ushio Sankawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     ´ó¶¹ÜÕÔª
C15H10O4     ÏàËÆ¶È:63.1%
Chinese Traditional and Herbal Drugs          2009          40          865-868
Ðâëǧ½ï°Î¸ùµÄ»¯Ñ§³É·ÖÑо¿
ÕÅÑ©;ËÎÆôʾ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     7,4'-dimethoxyisoflavone
    ÏàËÆ¶È:63.1%
Chinese Traditional and Herbal Drugs          2005          36          1469-1471
×ÏË뻱ϸ°û¶¾»îÐÔ²¿Î»»¯Ñ§³É·ÖÑо¿
½ªãü,°×ÀöƼ,¿µÍ¢¹ú
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     isoformononetein
    ÏàËÆ¶È:63.1%
Chinese Traditional and Herbal Drugs          2001          32          489-490
Studies on chemical constituents of Hedysarum sikkimense var. rigidum
LI Yun sen; CHEN Ji jun; LIAO Xin rong; WANG Hui ying; LUO Shi de
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     compound 3
    ÏàËÆ¶È:63.1%
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

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34 .     Formononetin
    ÏàËÆ¶È:63.1%
Archives of Pharmacal Research          2005          28          190-194
Monoamine oxidase inhibitory components from the roots ofSophora flavescens
Ji-Sang Hwang, Seon A Lee, Seong Su Hong, Kyong Soon Lee and Myung Koo Lee, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     formononetin
    ÏàËÆ¶È:63.1%
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

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36 .     formonoetin
    ÏàËÆ¶È:63.1%
Chinese Pharmaceutical Journal          2009          44          897-899
Studies on Chemical Constituents of Alhagi pseudalhagi(M.B.)
ZHANG Gui-jie, LI Ning, XIONG Yuan-jun, LI Xian, LI Yong, JIA Xiao-guang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     daidzein dimethy ether
    ÏàËÆ¶È:63.1%
Chinese Journal of Medicinal Chemistry          2003          13          215-218
Isolation and identification of pterocarpans and isoflavones from the pericarp of Sphaerophysa salsula DC.
LI Guo-yu, WANG Jin-hui, LI Xian, LI Ning
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     4',7-Dimethoxy-3'-iodoisoflavone
C17H13IO4     ÏàËÆ¶È:63.1%
Heterocycles          2011          82          1489-1501
Synthesis of New Biheterocycles by a One-Pot Sonogashira Coupling Reaction
Mandar Deodhar, David StC Black,* and Naresh Kumar*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     1,2-Bis-(4',7-dimethoxyisoflavone-3'-yl)ethyne
C36H26O8     ÏàËÆ¶È:63.1%
Heterocycles          2011          82          1489-1501
Synthesis of New Biheterocycles by a One-Pot Sonogashira Coupling Reaction
Mandar Deodhar, David StC Black,* and Naresh Kumar*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     formononetin
    ÏàËÆ¶È:63.1%
Journal of the Chemical Society, Perkin Transactions 1          1982                   2725-2734
Studies on plant tissue cultures. Part 36. Biosynthesis of a retrochalcone, echinatin, and other flavonoids in the cultured cells of Glycyrrhiza echinata. A new route to a chalcone with transposed A- and B-rings
Shin-ichi Ayabe and Tsutomu Furuya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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41 .     6-allyl-3-(benzo[d][1,3]dioxol-5-yl)-7-hydroxy-4H-chromen-4-one
C19H14O5     ÏàËÆ¶È:63.1%
Bioorganic & Medicinal Chemistry          2010          18          249-266
The synthesis and evaluation of flavone and isoflavone chimeras of novobiocin and derrubone
Jared R. Mays, Stephanie A. Hill, Justin T. Moyers, Brian S.J. Blagg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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42 .     corylin
    ÏàËÆ¶È:63.1%
Food Chemistry          2005          91          287-292
Antioxidants from a Chinese medicinal herb ¨C Psoralea corylifolia L
Guo Jiangning, Weng Xinchu, Wu Hou, Li Qinghua, Bi Kaishun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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43 .     7-Ethoxy-3-(4-methoxy-3-nitrophenyl)-4H-chromen-4-one
    ÏàËÆ¶È:63.1%
European Journal of Medicinal Chemistry          2012          54          175-187
Synthesis and antitumor activity of formononetin nitrogen mustard derivatives
Jie Ren, Hua-Jin Xu, Hong Cheng, Wen-Qun Xin, Xin Chen, Kun Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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44 .     7-Propoxy-3-(4-methoxy-3-nitrophenyl)-4H-chromen-4-one
    ÏàËÆ¶È:63.1%
European Journal of Medicinal Chemistry          2012          54          175-187
Synthesis and antitumor activity of formononetin nitrogen mustard derivatives
Jie Ren, Hua-Jin Xu, Hong Cheng, Wen-Qun Xin, Xin Chen, Kun Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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45 .     7-Isopropoxy-3-(4-methoxy-3-nitrophenyl)-4H-chromen-4-one
    ÏàËÆ¶È:63.1%
European Journal of Medicinal Chemistry          2012          54          175-187
Synthesis and antitumor activity of formononetin nitrogen mustard derivatives
Jie Ren, Hua-Jin Xu, Hong Cheng, Wen-Qun Xin, Xin Chen, Kun Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

46 .     7-Allyloxy-3-(4-methoxy-3-nitrophenyl)-4H-chromen-4-one
    ÏàËÆ¶È:63.1%
European Journal of Medicinal Chemistry          2012          54          175-187
Synthesis and antitumor activity of formononetin nitrogen mustard derivatives
Jie Ren, Hua-Jin Xu, Hong Cheng, Wen-Qun Xin, Xin Chen, Kun Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

47 .     7-(Cyclopentyloxy)-3-(4-methoxy-3-nitrophenyl)-4H-chromen-4-one
    ÏàËÆ¶È:63.1%
European Journal of Medicinal Chemistry          2012          54          175-187
Synthesis and antitumor activity of formononetin nitrogen mustard derivatives
Jie Ren, Hua-Jin Xu, Hong Cheng, Wen-Qun Xin, Xin Chen, Kun Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

48 .     7-Ethoxy-3-(3-amino-4-methoxyphenyl)-4H-chromen-4-one
    ÏàËÆ¶È:63.1%
European Journal of Medicinal Chemistry          2012          54          175-187
Synthesis and antitumor activity of formononetin nitrogen mustard derivatives
Jie Ren, Hua-Jin Xu, Hong Cheng, Wen-Qun Xin, Xin Chen, Kun Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

49 .     7-Propoxy-3-(3-amino-4-methoxyphenyl)-4H-chromen-4-one
    ÏàËÆ¶È:63.1%
European Journal of Medicinal Chemistry          2012          54          175-187
Synthesis and antitumor activity of formononetin nitrogen mustard derivatives
Jie Ren, Hua-Jin Xu, Hong Cheng, Wen-Qun Xin, Xin Chen, Kun Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

50 .     7-Allyloxy-3-(3-amino-4-methoxyphenyl)-4H-chromen-4-one
    ÏàËÆ¶È:63.1%
European Journal of Medicinal Chemistry          2012          54          175-187
Synthesis and antitumor activity of formononetin nitrogen mustard derivatives
Jie Ren, Hua-Jin Xu, Hong Cheng, Wen-Qun Xin, Xin Chen, Kun Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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51 .     3-(3-(Bis(2-chloroethyl)amino)-4-methoxyphenyl)-7-hydroxy-4H-chromen-4-one
    ÏàËÆ¶È:63.1%
European Journal of Medicinal Chemistry          2012          54          175-187
Synthesis and antitumor activity of formononetin nitrogen mustard derivatives
Jie Ren, Hua-Jin Xu, Hong Cheng, Wen-Qun Xin, Xin Chen, Kun Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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52 .     2 ,7-dihydroxy-4 -methoxy-5 -(3-methylbut-2-enyl)isoflavone
C21H20O5     ÏàËÆ¶È:61.9%
Chemical & Pharmaceutical Bulletin          2008          56(1)          85-88
Prenylated Flavonoids with PTP1B Inhibitory Activity from the Root Bark of Erythrina mildbraedii
JunPil JANG,MinKyun NA,Phuong Thien THUONG,Dieudonn¨¦ NJAMEN,Joseph Tanyi MBAFOR,Zacharias Tanee FOMUM,Eun-Rhan WOO,and Won Keun OH
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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53 .     7-Benzyloxy-3-(4-methoxy-3-nitrophenyl)-4H-chromen-4-one
    ÏàËÆ¶È:61.9%
European Journal of Medicinal Chemistry          2012          54          175-187
Synthesis and antitumor activity of formononetin nitrogen mustard derivatives
Jie Ren, Hua-Jin Xu, Hong Cheng, Wen-Qun Xin, Xin Chen, Kun Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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54 .     erylatissin B
C20H16O5     ÏàËÆ¶È:60%
Phytochemistry          2005          66          99-104
Antimicrobial and radical scavenging flavonoids from the stem wood of Erythrina latissima
Musa Chacha, Gomotsang Bojase-Moleta, Runner R.T. Majinda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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55 .     coniferaldehyde
    ÏàËÆ¶È:60%
Phytochemistry          2009          70          147-155
On the role of the monolignol ¦Ã-carbon functionality in lignin biopolymerization
Anders Holmgren, Magnus Norgren , Liming Zhang , Gunnar Henriksson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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56 .     norisojamaicin
C20H14O6     ÏàËÆ¶È:60%
Phytochemistry          1998          47          295-300
Rotenoids, isoflavones and chalcones from the stem bark of Millettia usaramensis subspecies usaramensis
Abiy Yenesew, Jacob O. Midiwo, Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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