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PSA: ½ð±Ò+1, 3u 2013-08-30 15:04:29
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1 .     balanophonin
C20H20O6     ÏàËÆ¶È:85%
Chemistry of Natural Compounds          2009          45          536-538
CHEMICAL CONSTITUENTS FROMTHE STEM BARK OF Trewia nudiflora
Shao-Hua Wu, Yue-Mao Shen, You-Wei Chen, Zhi-Ying Li, Li-Yuan Yang, and Shao-Lan Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-3-hydroxymethyl-7-methoxybenzofuran-5-(trans)propenicacid
C20H20O7     ÏàËÆ¶È:85%
Phytochemistry          1996          43          1349-1354
Dihydrobenzofuran lignans from Boreava orientalis
Akiyo Sakushima, Maksut Cokun, Takashi Maoka, Sansei Nishibe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     cimicifugic acid
C20H20O7     ÏàËÆ¶È:85%
Acta Pharmaceutica Sinica          2002          Vol 37          535-538
STUDIES ON THE PHENOLIC ACID CONSTITUENTS FROM CHINESE MEDICINE ¡°SHENG-MA¡±,RHIZOME OF CIMICIFUGA FOETIDA L.
ZHAO Xiao-hong; CHEN Di-hua; SI Jian-yong; PAN Rui-le; SHEN Lian-gang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     glycosmisic acid
    ÏàËÆ¶È:85%
Chinese Traditional and Herbal Drugs          2010          41          509-514
A new lignan from Gardenia jasminoides
YU Yang; GAO Hao; DAI Yi; LI Xiao-xia; LI Jia-ming; YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     balanophonin
    ÏàËÆ¶È:85%
Journal of the Chinese Chemical Society          2003          50          1271-1274
Neolignans from the Parasitic Plants. Part 1. Aeginetia indica
Jiau-Ching Ho, Chiu-Ming Chen and Lie-Ching Row
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     avellanedae A
C20H20O7     ÏàËÆ¶È:85%
Fitoterapia          2012          83          1484-1488
Anti-inflammatory constituents from Tabebuia avellanedae
Maorong Suo, Hasegawa Isao, Hikaru Kato, Fumihide Takano, Tomihisa Ohta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     É½éÙÖ¬Ëá
    ÏàËÆ¶È:85%
Chinese Pharmaceutical Journal          2012          47          1029-1031
Study on Chemical Constituents of Alocasia macrorrhiza(L.) Schott
ZHU Ling-hua; HUANG Xiao-sheng; YE Wen-cai; ZHOU Guang-xiong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     rel-(7R,7'E,8S)-4,9-Dihydroxy-3,3',5-trimethoxy-4',7-epoxy-8,5'-neolign-7'-en-9'-oic Acid
C21H22O8     ÏàËÆ¶È:83.3%
Helvetica Chimica Acta          2010          93          2467-2477
Neolignans and Caffeoyl Derivatives from Selaginella moellendorffii
Yue-Hu Wang, Qian-Yun Sun, Fu-Mei Yang, Chun-Lin Long, Fu-Wei Zhao, Gui-Hua Tang, Hong-Mei Niu, Huan Wang, Qiao-Qin Huang, Jin-Jin Xu and Li-Juan Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     diospyrosin
C20H18O5     ÏàËÆ¶È:80%
Chemistry & Biodiversity          2008          Vol. 5          2442
Study of Antimalarial Activity of Chemical Constituents from Diospyros quaesita
Cui-Ying Ma, Sebisubi Fred Musoke, Ghee Teng Tan, Kongmany Sydara, Somsanith Bouamanivong, Bounhoong Southavong, D. Doel Soejarto, Harry H. S. Fong, and Hong-Jie Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     balanophonin
    ÏàËÆ¶È:80%
Chinese Traditional and Herbal Drugs          2010          41          509-514
A new lignan from Gardenia jasminoides
YU Yang; GAO Hao; DAI Yi; LI Xiao-xia; LI Jia-ming; YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
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PSA: ½ð±Ò+1, 3u 2013-08-30 15:04:38
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1 .     nobiletin
C9H12O2     ÏàËÆ¶È:90.4%
Molecules          2013          18          4766-4775
Chemical Constituents of the Root of Jasminum giraldii
Zhenggang Yue, Hui Qin, Yuhua Li, Yang Sun, Zhipeng Wang, Tiehong Yang, Li Liu, Minchang Wang, Feng Feng and Qibing Mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     nobiletin
    ÏàËÆ¶È:80.9%
Acta Botanica Sinica          1996          38          161-166
Chemical Constituents from Roots of Jatropha curcas
Kong Ling-yi, Min Zhi-da and Shi Jian-xia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Nobiletin
    ÏàËÆ¶È:76.1%
Lishizhen Medicine and Materia Medica Research          2010          21          2469-2470
Study on the Compounds of Polymethoxylated Flavonoids in Fructus Aurantii Immaturus
HAN Jin-dan; WANG Kui-wu; SHEN Lian-qing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     3,5,6,7,8,3',4'-Heptamethoxyflavone
    ÏàËÆ¶È:72.7%
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
5 .     5,3'-dihydroxy-3,6,7,8,4'-pentamethoxyflavone
    ÏàËÆ¶È:71.4%
Journal of Natural Products          1994          Vol 57          1012
Antimitotic and Cytotoxic Flavonols from Zieridium pseudobtusifolium and Acronychia porteri
Johannes J. Lichius, Odile Thoison, Alain Montagnac, Mary Païs, Françoise Gu¨¦ritte-Voegelein, Thierry S¨¦venet, Jean-Pierre Cosson, Abdul Hamid A. Hadi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     isoimerubrine
    ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1993          41          1418-1422
Structures and Solid State Tautomeric Forms of Two Novel Antileukemic Tropoloisoquinoline Alkaloids, Pareirubrines A and B, from Cissampelos pareira
Hiroshi MORITA,Kouji MATSUMOTO,Koichi TAKEYA,Hideji ITOKAWA and Yoichi IITAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     5,3'-dihydroxy-3,6,7,8,4'-pentamethoxyflavone
C20H20O9     ÏàËÆ¶È:66.6%
Journal of Natural Products          1995          Vol 58          475-482
Antitumor Agents, 154. Cytotoxic and Antimitotic Flavonols from Polanisia dodecandra
Qian Shi, Ke Chen, Leping Li, Jer-Jang Chang, Cari Autry, Mutsuo Kozuka, Takao Konoshima, James R. Estes, Chii M. Lin, Ernest Hamel, Andrew T. McPhail, Donald R. McPhail, Kao-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     3'-Formyl-5-hydroxy-3,6,7,8,4'-pentamethoxy-flavone
C21H20O9     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry          2011          19          186-196
Synthesis of antiproliferative flavones from calycopterin, major flavonoid of Calycopteris floribunda Lamk.
Guy Lewin, Narayan Bhat Shridhar, Genevi¨¨ve Aubert, Sylviane Thoret, Joëlle Dubois,Thierry Cresteil
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     3'-demethylnobiletin
C20H20O8     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry Letters          2011          21          4540-4544
Nobiletin metabolites: Synthesis and inhibitory activity against matrix metalloproteinase-9 production
Tetsuta Oshitari, Yuji Okuyama, Yoshiki Miyata, Hiroshi Kosano, Hideyo Takahashi, Hideaki Natsugari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     3-(3',4'-dimethoxyphenyl)-5,6,7-trimethoxychromen-4-one
C20H20O7     ÏàËÆ¶È:66.6%
Natural Product Research and Development          2010          22          956-960
Synthesis of the Natural Product 5,6,7,3 ,4 -Pentamethoxyisoflavone
REN Wan-li; CHEN Rui; JIN Ye; ZHANG Tao; LI Hong-qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     3-hydroxy-5,6,7,8,3',4'-hexamethoxyflavone
    ÏàËÆ¶È:66.6%
Journal of the Chinese Chemical Society          1998          45          89-91
Isolation and Characterization of an Antibacterial Substance from Citrus Plant
Chihiro Ito;Kazuko Fujiwara;Meisaku Koizumi;Hiroshi Furukawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     5-hydroxy-3,6,7,8,3',4'-hexamethoxyflavone
    ÏàËÆ¶È:66.6%
Food Chemistry          2011          127          394-403
Chemical composition and biological activity of Citrus jambhiri Lush
Dalia Hamdan, Mahmoud Zaki El-Readi, Ahmad Tahrani, Florian Herrmann, Dorothea Kaufmann, Nawal Farrag, Assem El-Shazly, Michael Wink
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     casticin
    ÏàËÆ¶È:66.6%
Phytotherapy Research          2007          21          391-394
Diterpenoids and flavonoids from the fruits of Vitex agnus-castus and antioxidant activity of the fruit extracts and their constituents
Zsuzsanna Hajd¨², Judit Hohmann, Peter Forgo, Tam¨¢s Martinek, M¨¢t¨¦ Dervarics, Istv¨¢n Zupk¨®, György Falkay, Daniel Cossuta and Imre M¨¢th¨¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     3',4,4',5,6-Pentamethoxyaurone
C20H20O7     ÏàËÆ¶È:66.6%
Journal of Agricultural and Food Chemistry          2007          55          700-705
Synthesis and Insect Antifeedant Activity of Aurones against Spodoptera litura Larvae
Masanori Morimoto, Hiromi Fukumoto, Toki Nozoe, Ai Hagiwara, and Koichiro Komai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     5-Hydroxy-6,7,8,3',4'-pentamethoxyflavone
    ÏàËÆ¶È:66.6%
Journal of Agricultural and Food Chemistry          1997          45          364-368
Two New Polymethoxylated Flavones, a Class of Compounds with Potential Anticancer Activity, Isolated from Cold Pressed Dancy Tangerine Peel Oil Solids
Jie Chen, Antonio M. Montanari, and Wilbur W. Widmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
3Â¥2013-08-29 22:13:51
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4Â¥: Originally posted by alsjione at 2013-08-30 05:55:07
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