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1

1 .     gentisein
    ÏàËÆ¶È:76.9%
China Journal of Chinese Materia Medica          2009          34          2338-2342
Chemical constituents from twigs of Garcinia xipshuanbannaensis
NA Zhi, XU Youkai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Gentisein
C13H8O5     ÏàËÆ¶È:76.9%
Journal of Natural Medicines          2007          61          269-279
The chemical constituents of fresh Gentian Root
Hidehiro Ando, Yasuaki Hirai, Mikio Fujii, Yumiko Hori and Motonori Fukumura, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     gentisein
    ÏàËÆ¶È:76.9%
Pharmacy and Pharmacology Communications          1998          4          415-417
Xanthones and Flavonoids of Polygala caudata
WENKUI LI, CHILEUNG CHAN, HIWUN LEUNG, HINWING YEUNG and PEIGEN XIAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     1,3,5-trihydroxyxanthone
    ÏàËÆ¶È:69.2%
Chinese Pharmaceutical Journal          2007          42          418-436
Study on Xanthones from Hypericum samponii Hance
GUO Cheng, ZHENG Qing-ming, ZHENG Han-chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     1,3,5-trihydroxyxanthone
    ÏàËÆ¶È:69.2%
Natural Product Research and Development          2004          16          511-513
XANTHONES FROM THE WHOLE PLANT OF HYPERICUM JAPONICUM
FU Peng; LI Ting-zhao; LIU Run-hui; ZHANG Wei; ZHANG Wei-dong*; CHEN Hai-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     isogentisin
    ÏàËÆ¶È:64.2%
Phytochemistry          1988          27          3696-3699
Two xanthone glycosides from Gentiana lutea
Takaaki Hayashi,Takashi Yamagishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Isogentisin
C14H10O5     ÏàËÆ¶È:64.2%
Journal of Natural Medicines          2007          61          269-279
The chemical constituents of fresh Gentian Root
Hidehiro Ando, Yasuaki Hirai, Mikio Fujii, Yumiko Hori and Motonori Fukumura, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     apigenin
    ÏàËÆ¶È:61.5%
Chinese Pharmaceutical Journal          2011          46          338-340
Study on Chemical Constituents of Lonicerae Japonicae Flos
FENG Wei-shenga, CHEN Xinga, ZHENG Xiao-keb, ZHANG Chun-lei, LI Dan-dana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     1,3,6,7-tetrahydroxyxanthonin
    ÏàËÆ¶È:61.5%
Natural Product Research and Development          2004          16          511-513
XANTHONES FROM THE WHOLE PLANT OF HYPERICUM JAPONICUM
FU Peng; LI Ting-zhao; LIU Run-hui; ZHANG Wei; ZHANG Wei-dong*; CHEN Hai-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     1,3,6,7-tetrahydroxyxanthonin
    ÏàËÆ¶È:61.5%
Bioorganic & Medicinal Chemistry          2012          20          4164-4171
Natural products as a gold mine for selective matrix metalloproteinases inhibitors
Liyan Wang, Xi Li, Shoude Zhang, Weiqiang Lu, Sha Liao, Xiaofeng Liu, Lei Shan, Xu Shen, Hualiang Jiang, Weidong Zhang, Jin Huang, Honglin Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     1,3,6-trihydroxy-5-methoxyxanthone
    ÏàËÆ¶È:57.1%
Planta Medica          2002          68          49-54
Natural Products Inhibiting Candida albicans Secreted Aspartic Proteases from Tovomita krukovii
Zhizhen Zhang,Hala N.ElSohly,Melissa R.Jacob,David S.Pasco,Larry A.Walker, Alice M.Clark
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     isogentisein
C14H10O5     ÏàËÆ¶È:57.1%
Natural Product Communications          2009          4          803-808
Globulixanthone F, a New Polyoxygenated Xanthone withan Isoprenoid group and two Antimicrobial Biflavonoidsfrom the Stem Bark of Symphonia globulifera
Pierre Mkounga, Zacharias T. Fomum, Mich¨¨le Meyer, Bernard Bodo and Augustin E. Nkengfack
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     1,3,6, 7-tetrahydroxyxanthone
    ÏàËÆ¶È:53.8%
Planta Medica          1991          57          172-175
Structures of Four New Isoprenylated Xanthones,Cudraxanthones L, M, N, and O from Cudrania tricuspidata
Yoshio Hano, Yutaka Matsumoto, Kazuko Shinohara, Jin-Yun Sun, and Taro Nomura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     Myricetin
    ÏàËÆ¶È:53.8%
Chemistry of Natural Compounds          2006          42          232-234
FLAVONOIDS OF Limonium aureum
Guan Ye and Chenggang Huang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Genistein
    ÏàËÆ¶È:53.8%
Molecules          2002          7          817-832
Phytoalexin Accumulation in Colombian Bean Varieties and Aminosugars as Elicitors
Diego Durango, Winston Quiñones, Fernando Torres, Yoni Rosero, Jes¨²s Gil and Fernando Echeverri
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound 3
    ÏàËÆ¶È:53.8%
Natural Product Research          1995          6          203-207
Genistein-C-Glucosides from Genista cinerea
I. Van Rensen; M. Veit; V. Wray; F. -C. Czygan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     genistein
    ÏàËÆ¶È:53.8%
China Journal of Chinese Materia Medica          2009          34          3217-3220
Isoflavones fromvines of Pueraria lobata
ZHANG Dewu, REN Yan, DAI Shengjun, LIU Wanhui, LI Guihai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     1,3,5-trihydroxy-2-methoxyxanthone
    ÏàËÆ¶È:53.8%
China Journal of Chinese Materia Medica          2007          32          692-694
Studies on flavonoids from stems and leaves of Calophyllum inophyllum
LI Yanzhi, LI Zhanlin, HUA Huiming, LI Zhenggang, LIU Mingsheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     quercetin
    ÏàËÆ¶È:53.8%
Acta Pharmaceutica Sinica          2002          Vol 37          352-354
STUDIES ON THE CHEMICAL CONSTITUENTS OF PSEUDOTSUGA SINENSIS
YI Jin hai; ZHANG Guo lin; LI Bo gang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     genistein
    ÏàËÆ¶È:53.8%
Natural Product Sciences          2006          12          109-112
Antiproliferative Constituents from the Vinegar Treated Small Black Soybean (Glycine max Merr.)
Oh, Chan-Ho; Kim, Eun-Jeong; Lee, Kyu-Hee; Moon, Mi-Kyeong; Cho, Moon-Gu; Kim, Jong-Hwa; Oh, Suk-Heung; Lee, Tae-Kyoo; Shin, Tae-Yong; Kim, Dae-Keun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     genistein
    ÏàËÆ¶È:53.8%
Chemical & Pharmaceutical Bulletin          1987          35          4846-4850
Studies on the Constituents of Pueraria lobata. III. Isoflavonoids and Related Compounds in the Roots and the Voluble Stems
JUN-EI KINJO,JUN-ICHI FURUSAWA,JUNKO BABA,TAKASHI TAKESHITA,MASAKI YAMASAKI and TOSHIHIRO NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     mangiferin
C13H8O6     ÏàËÆ¶È:53.8%
Phytochemistry          1989          28          1289-1290
A bacterial cleavage of the C-glucosyl bond of mangiferin and bergenin
Masao Hattori,Yue-Zhong Shu,Tsuyoshi Tomimori,Kyoichi Kobashi,Tsuneo Namba
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     kaempferol
C15H10O6     ÏàËÆ¶È:53.8%
Chinese Traditional and Herbal Drugs          2010          41          1258-1260
ºìҶľ½ª×ÓÆ¤µÄ»¯Ñ§³É·ÖÑо¿
ÂÞÒÕÆ¼;ÕÔÐËÌÃ;ÍõÀö;ÑòÏþ¶«;ÕÔ¾²·å;ÀîÁ¼
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     1,8-¶þôÇ»ù-3,5-¶þ¼×Ñõ»ùÉÇͪ
    ÏàËÆ¶È:53.8%
Chinese Traditional and Herbal Drugs          2007          38          344-346
Xanthone constituents in Gentiana panthaica
YANG Hong-peng; LIU Xia; SHI Yan-ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     genistein
    ÏàËÆ¶È:53.8%
Chinese Traditional and Herbal Drugs          2006          37          350-352
¸ð»¨»¯Ñ§³É·ÖµÄÑо¿(¢ñ)
Òü¿¡Í¤;ÖÙÓ¢;Ëï¾´ÓÂ;Áõ³;Íõ±ò
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     5,7,4-ÈýôÇ»ùÒì»ÆÍª
C15H10O5     ÏàËÆ¶È:53.8%
Chinese Traditional and Herbal Drugs          2005          36          184-185
º£·çÌٵĻ¯Ñ§³É·ÖÑо¿(¢ñ)
ÈηçÖ¥,ÕÅÀö,Å£¹ðÔÆ,Áõ¸ÕÈþ,¶Îº£Çå
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     Genistein
    ÏàËÆ¶È:53.8%
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
28 .     Kaempferol
C15H10O6     ÏàËÆ¶È:53.8%
Archives of Pharmacal Research          2010          33          1665-1670
Cholinesterase inhibitors from Cleistocalyx operculatus buds
Byung Sun Min, To Dao Cuong, Joo-Sang Lee, Beom-Soo Shin and Mi Hee Woo, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     compound 18
C13H10O4     ÏàËÆ¶È:53.8%
Tetrahedron Letters          2001          42          3283-3286
An unexpected ring-opening of a 2-pyrone ring at low temperatures. A mild and expeditious synthesis of novel coumarins
Ossama Saleh Darwish, Kirsten A Granum, Quang Tan, Richard P Hsung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     1,3,6,7-tetrahydroxy-xanthone
    ÏàËÆ¶È:53.8%
Chinese Pharmaceutical Journal          2007          42          418-436
Study on Xanthones from Hypericum samponii Hance
GUO Cheng, ZHENG Qing-ming, ZHENG Han-chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     4',5,7-trihydroxyisoflavone
    ÏàËÆ¶È:53.8%
Chinese Journal of Medicinal Chemistry          2011          21          227-231
Study on the secondary metabolites from a marine-derived actinomycete Streptomyces sp£®
LI Bin, CHEN Gang, BAI Jiao, PEI Yue-hu*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     genistein
    ÏàËÆ¶È:53.8%
Journal of China Pharmaceutical University          2001          32          197-199
Studies on the Constituents of Belamcanda chinensis(¢ñ)
JI Wen Liang; QIN Min Jian; WANG Zheng Tao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     2-Hydroxy-N-(2-hydroxy-3-nitrophenyl)-3-nitrobenzamide
    ÏàËÆ¶È:53.8%
Zeitschrift f¨¹r Naturforschung B          2011          66          479-486
Synthesis of Substituted Benzoxazolinones by the Curtius Rearrangement: Crystal Structures of Intermediates and By-Products
G. Laus, V. Kahlenberg, K. Wurst, S. Nerdinger, and H. Schottenberger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     myricetin
    ÏàËÆ¶È:53.8%
Natural Product Research and Development          2007          19          67-69
Study on the Chemical Constituents of Sedum aizoon L.
YU Zhi-bin; YANG Guang-yi; WU Xia;ZHOU Ya-wei*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     genistein
    ÏàËÆ¶È:53.8%
Natural Product Research and Development          2005          17          595-597
Studies on the Chemical Constituents of Isoflavone from the Flowers of Pueraria lobata
ZHANG Shu-ping; ZHANG Zun-ting
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     myricetin
    ÏàËÆ¶È:53.8%
Natural Product Research and Development          2005          17          583-584
Pheonlic Constituents from the Whole Plants of Limonium aureum
YE Guan; FAN Ming-song; HUANG Cheng-gang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     genistein
C15H10O5     ÏàËÆ¶È:53.8%
Journal of Integrative Plant Biology          2005          47          1404-1408
A New Isoflavonoid from Belamcanda chinensis (L.) DC.
Min-Jian QIN*, Wen-Liang JI, Zheng-Tao WANG and Wen-Cai YE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     genistein
C15H10O5     ÏàËÆ¶È:53.8%
Journal of Integrative Plant Biology          2006          48          996-1000
Water-Soluble Constituents of Cudrania tricuspidata (Carr.) Bur.
Zong-Ping Zheng, Jing-Yu Liang and Li-Hong Hu*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     K-254-I(4',5,7-trihydroxyisoflavone)
C15H10O5     ÏàËÆ¶È:53.8%
Agricultural and Biological Chemistry          1987          51          3003-3009
K-254-I (Genistein), a New Inhibitor of Ca2+ and Calmodulin-Dependent Cyclic Nucleotide Phosphodiesterase from Streptosporangium vulgare
Joji GOTO, Yuzuru MATSUDA, Kozo ASANO, Isao KAWAMOTO, Tohru YASUZAWA, Kunikatsu SHIRAHATA, Hiroshi SANO, Hiroshi KASE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     genistein
    ÏàËÆ¶È:53.8%
Food Chemistry          2012          131          161-169
Changes occurring in compositional components of black soybeans maintained at room temperature for different storage periods
Jin Hwan Lee, Kye Man Cho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     genistein
    ÏàËÆ¶È:53.8%
Food Chemistry          2009          114          869-873
Isolation and characterisation of the isoflavones from sprouted chickpea seeds
Shuhui Zhao, Linping Zhang, Peng Gao, Zhiyu Shao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     N-(6-nitro-1,3-benzothiazol-2-yl)-N'-(2-thioxo-2,3-dihydro-2¦Ë5-pyrido[2,3-d][1,3,2]oxazaphosphol-2-yl)guanidine
C13H10N7O3S2P     ÏàËÆ¶È:53.8%
Chemical & Pharmaceutical Bulletin          2013          69          25-32
Synthesis of Novel Phosphorylated Guanidine Derivatives from Cyanamide and Their Anti-inflammatory Activity
Venkata Ramana Katla, Rasheed Syed, Chandra Sekhar Kuruva, Hema Kumar Kuntrapakam, Naga Raju Chamarthi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     N-[4-(6-Bromobenzo[d]thiazol-2-yl)phenyl]-N-methylformamide
C15H11BrN2OS     ÏàËÆ¶È:53.8%
European Journal of Organic Chemistry          2012                   1303-1310
Rapid Room-Temperature 11C-Methylation of Arylamines with [11C]Methyl Iodide Promoted by Solid Inorganic-Bases in DMF
Lisheng Cai, Rong Xu, Xuelei Guo and Victor W. Pike
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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2

1 .     Isogentisin
C14H10O5     ÏàËÆ¶È:92.8%
Journal of Natural Medicines          2007          61          269-279
The chemical constituents of fresh Gentian Root
Hidehiro Ando, Yasuaki Hirai, Mikio Fujii, Yumiko Hori and Motonori Fukumura, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     isogentisin
    ÏàËÆ¶È:85.7%
Phytochemistry          1988          27          3696-3699
Two xanthone glycosides from Gentiana lutea
Takaaki Hayashi,Takashi Yamagishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     isogentisein
C14H10O5     ÏàËÆ¶È:85.7%
Natural Product Communications          2009          4          803-808
Globulixanthone F, a New Polyoxygenated Xanthone withan Isoprenoid group and two Antimicrobial Biflavonoidsfrom the Stem Bark of Symphonia globulifera
Pierre Mkounga, Zacharias T. Fomum, Mich¨¨le Meyer, Bernard Bodo and Augustin E. Nkengfack
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     1,3-dihydroxy-7-methoxyxanthone
    ÏàËÆ¶È:78.5%
Phytochemistry          1998          48          725-728
Three xanthones from Polygala cyparissias
Tania R. Pinheiro, Valdir Cechinel Filho, Adair R. S. Santos, João B. Calixto, Franco Delle Monache, Moacir G. Pizzolatti, Rosendo A. Yunes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     gentisein
    ÏàËÆ¶È:71.4%
China Journal of Chinese Materia Medica          2009          34          2338-2342
Chemical constituents from twigs of Garcinia xipshuanbannaensis
NA Zhi, XU Youkai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Gentisein
C13H8O5     ÏàËÆ¶È:71.4%
Journal of Natural Medicines          2007          61          269-279
The chemical constituents of fresh Gentian Root
Hidehiro Ando, Yasuaki Hirai, Mikio Fujii, Yumiko Hori and Motonori Fukumura, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     1,3,5-trihydroxyxanthone
    ÏàËÆ¶È:71.4%
Natural Product Research and Development          2004          16          511-513
XANTHONES FROM THE WHOLE PLANT OF HYPERICUM JAPONICUM
FU Peng; LI Ting-zhao; LIU Run-hui; ZHANG Wei; ZHANG Wei-dong*; CHEN Hai-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     gentisein
    ÏàËÆ¶È:71.4%
Pharmacy and Pharmacology Communications          1998          4          415-417
Xanthones and Flavonoids of Polygala caudata
WENKUI LI, CHILEUNG CHAN, HIWUN LEUNG, HINWING YEUNG and PEIGEN XIAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     1-hydroxy-3, 7-dimethoxyxanthone
    ÏàËÆ¶È:66.6%
Planta Medica          1994          60          507-511
Bellidifolin: A Potent Hypoglycemic Agent in Streptozotocin (STZ)-Induced Diabetic Rats from Swertiajaponica
PurusotamBasnet, Shigetoshi Kadota, Mineo Shimnizu, and TsuneoNamba
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     1-hydroxy-3,7-dimethoxyxanthone
    ÏàËÆ¶È:66.6%
Fitoterapia          2001          72          715-716
A xanthone from Shultesia guianensis
F.J.Q. Monte, F.P. Soares, R. Braz-Filho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     1,3,6-trihydroxy-5-methoxyxanthone
    ÏàËÆ¶È:64.2%
Planta Medica          2002          68          49-54
Natural Products Inhibiting Candida albicans Secreted Aspartic Proteases from Tovomita krukovii
Zhizhen Zhang,Hala N.ElSohly,Melissa R.Jacob,David S.Pasco,Larry A.Walker, Alice M.Clark
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     1,3,5-trihydroxyxanthone
    ÏàËÆ¶È:64.2%
Chinese Pharmaceutical Journal          2007          42          418-436
Study on Xanthones from Hypericum samponii Hance
GUO Cheng, ZHENG Qing-ming, ZHENG Han-chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     gentisin
    ÏàËÆ¶È:64.2%
Chinese Journal of Medicinal Chemistry          2010          20          125-128
Isolation and identification of the Chemical constituents from Swertia yunnanensis Burk.
YU Ying, WANG Shi-sheng*, DING Feng-uan, ZHU Jing-bo, ZHAO Wei-jie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     2'-hydroxygenistein
    ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1993          41          394-396
Three New Isoflavonoid Glycosides from Lupinus luteus and L. polyphyllus¡Áarboreus
Kazutaka WATANABE,Junei KINJO and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     luteolin-7-O-neohesperidoside
    ÏàËÆ¶È:60%
China Journal of Chinese Materia Medica          2009          34          1377-1380
¼ÙŠL°üÒ¶¿¹¾ú»îÐԳɷֵÄÑо¿(2)
ÌïÒ±, ÌÀº£·å, ÍõÏþ¾ê, Çñ·å , Ѧ¸Ä½ø, Àî¾ü
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     5,3'-dihydroxy-4'-methoxy-7-carbomethoxyflavonol
C18H16O8     ÏàËÆ¶È:60%
Journal of Natural Products          1993          Vol 56          1164
Anti-Inflammatory Activity of Two Flavonoids from Tanacetum microphyllum
M. J. Abad, P. Bermejo, A. Villar, S. Valverde
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     2',4',5,7-tetrahydroxyisoflavone
    ÏàËÆ¶È:60%
Acta Pharmaceutica Sinica          2008          Vol 43          67-70
Chemical constituents from Spatholobus sinensis
YIN Ting; LIU Hua; WANG Bin; TU Guang-zhong; LIANG Hong; ZHAO Yu-ying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     luteolin
C15H10O6     ÏàËÆ¶È:60%
Chinese Traditional and Herbal Drugs          2009          40          1540-1543
Chemical constituents of Artemisia frigida
WANG Qing-hu; WANG Jin-hui; Eerdunbagen; Tana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     2',4',5,7-Tetrahydroxyisoflavone
    ÏàËÆ¶È:60%
Archives of Pharmacal Research          2004          27          544-546
Flavonoids of crotalaria sessiliflora
Hun Sung Yoo, Ji Suk Lee, Chul Young Kim and Jinwoong Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     8-Carboxymethyl-1,3,5,6-tetrahydroxyxanthone
    ÏàËÆ¶È:60%
Molecules          2011          16          10479-10490
Chemical Constituents of the Methanolic Extract of Leaves of Leiothrix spiralis Ruhland and Their Antimicrobial Activity
Marcelo Gonzaga de Freitas Ara¨²jo, Felipe Hil¨¢rio, Leonardo Gorla Nogueira, Wagner Vilegas, Lourdes Campaner dos Santos and Ta¨ªs Maria Bauab
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     5,7,2',4'-tetrahydroxyisoflavone
    ÏàËÆ¶È:60%
Chemistry of Natural Compounds          2012          48          674-676
Isoflavonoids from Sophora tonkinensis
Rui-Yun Yang, Yan-Su Lan, Zhong-Jing Huang, Chang-Lun Shao and Hong Liang, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     1,3,7-trihydroxy-5-methoxyxanthone
C14H10O6     ÏàËÆ¶È:57.1%
Phytochemistry          2006          67          2146-2151
Xanthones from Hypericum chinense
Naonobu Tanaka, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     securixanthone C
C14H10O6     ÏàËÆ¶È:57.1%
Acta Botanica Sinica          2003          45          365-368
Two New Xanthones from the Stems of Securidaca inappendiculata
YANG Xue-Dong XU Li-Zhen YANG Shi-Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     1,4-dihydroxy-6,7-methylenedioxyxanthone
C14H8O6     ÏàËÆ¶È:57.1%
Chinese Chemical Letters          2005          16          623-624
Two New Xanthones from Polygala crotalarioides
Shi Ming DENG, You Xing ZHAO, Yu Qing LIU, Jun ZHOU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     1,7-dihydroxy-3-methoxyxanthone
C14H10O5     ÏàËÆ¶È:57.1%
Phytochemistry          1991          30          2061-2065
Two xanthones from Polygala tenuifolia
Yukinobu Ikeya, Kô Sugama, Minoru Okada, Hiroshi Mitsuhashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     1,2-dihydroxy-3-methoxyxanthone
    ÏàËÆ¶È:57.1%
Phytochemistry          1991          30          3625-3629
Xanthones fromChironia krebsii
Jean-luc Wolfender, Matthias Hamburger, Jerome D. Msonthi, Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     1,7-dihydroxy-3-methoxyxanthone
    ÏàËÆ¶È:57.1%
Phytochemistry          1991          30          3625-3629
Xanthones fromChironia krebsii
Jean-luc Wolfender, Matthias Hamburger, Jerome D. Msonthi, Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     1,4-dihydroxy-6,7-methylnedioxyxanthone
C14H8O6     ÏàËÆ¶È:57.1%
Chemical Research in Chinese Universities          2006          22          400-402
New Xanthones from Polygala crotalarioides
DENG Shi-ming, YANG Xian-hui, ZHAO You-xing and ZHOU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     N-(3,4-Dichlorophenyl)-2-(3-fluoro-4-nitrophenoxy)acetamide
C14H9Cl2FN2O4     ÏàËÆ¶È:57.1%
Molecules          2012          17          2248-2258
Synthesis and Biological Evaluation of 2-(3-Fluoro-4-nitro phenoxy)-N-phenylacetamide Derivatives as Novel Potential Affordable Antitubercular Agents
Wei Ang,Yan-Ni Lin,Tao Yang,Jian-Zhong Yang ,Wei-Yi Pi ,Ying-Hong Yang ,You-Fu Luo ,ong Deng and Yu-Quan Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     Gentisin
C14H10O5     ÏàËÆ¶È:57.1%
Journal of Natural Medicines          2007          61          269-279
The chemical constituents of fresh Gentian Root
Hidehiro Ando, Yasuaki Hirai, Mikio Fujii, Yumiko Hori and Motonori Fukumura, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     1,7-dihydroxy-3-methoxyxanthone
C14H10O5     ÏàËÆ¶È:57.1%
Chinese Traditional and Herbal Drugs          2005          36          1291-1293
Chemical constituents of Polygala tenuifolia
WANG Yu-ping; YANG Jun-shan; ZHANG Yu-mei; CHEN Jian-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     1,3,7,8-tetrahydroxyxanthone
    ÏàËÆ¶È:57.1%
Chinese Traditional and Herbal Drugs          2002          33          583-586
Studies on chemical constituents of Swertia przewalskii
PAN Li; ZHANG Xiao feng; WANG Ming kui; LIAO Zhi xin; DING Li sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     Kaempferol
C15H10O6     ÏàËÆ¶È:57.1%
Archives of Pharmacal Research          2010          33          1665-1670
Cholinesterase inhibitors from Cleistocalyx operculatus buds
Byung Sun Min, To Dao Cuong, Joo-Sang Lee, Beom-Soo Shin and Mi Hee Woo, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     1,7-¶þôÇ»ù-3-¼×Ñõ»ù¿Úɽͪ
C14H10O5     ÏàËÆ¶È:57.1%
Chinese Journal of Medicinal Chemistry          2012          22          511-515
Study on the cytotoxic chemical constituents from the twigs of Calophyllum inophyllum
ZENG Yan-bo; MEI Wen-li; ZHANG Xing; Li Xiao-na; DAI Hao-fu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     5,6',7-trihydroxy-3',4'-methylenedioxyisoflavone
    ÏàËÆ¶È:56.2%
Bulletin of the Korean Chemical Society          2004          25          147-148
New Isoflavone Glycoside from the Woods of Sophora japonica
Youngki Park*, Hak-Ju Lee, Sung-Suk Lee, Don-Ha Choi, Jung-Soo Oh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     luteolin
    ÏàËÆ¶È:53.3%
Planta Medica          1995          61          570-573
Constituents of the Egyptian Gentaurea scoparia; III. Phenolic Constituents of the Aerial Parts
Diaa Youssef and August W. Frahm
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     cinaroside
C21H20O11     ÏàËÆ¶È:53.3%
Chemistry of Natural Compounds          2002          38          358-406
PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria L. GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES
V. M. Malikov and M. P. Yuldashev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     Luteolin
C15H10O6     ÏàËÆ¶È:53.3%
Molecules          2008          13          1931-1941
Flavonoids and a New Polyacetylene from Bidens parviflora Willd
Yu-Lan Li, Jun Li, Nai-Li Wang and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     luteolin
    ÏàËÆ¶È:53.3%
Journal of Chinese Pharmaceutical Sciences          2000          9          134-136
Two Novel Flavonoids from Ixeris sonchifolia
Feng Xizhi, Xu Suixu and Dong Mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     luteolin
    ÏàËÆ¶È:53.3%
Journal of Chinese Pharmaceutical Sciences          2004          13          212-213
Flavones Isolated from Codonopsis xundianensis
HE Qing; ZHU En-yuan; WANG Zheng-tao; XU Luo-shan; and HU Zhi-bi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     luteolin
    ÏàËÆ¶È:53.3%
Natural Product Research          2009          23          1378-1383
A new acylated quercetin glycoside from the leaves of Stevia rebaudiana Bertoni
Jun Li; Hua Jiang; Renbing Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     luteolin
    ÏàËÆ¶È:53.3%
China Journal of Chinese Materia Medica          2009          34          3043-3046
Chemical constituents in Buddleja albiflora
TAO Liang, HUANG Jincheng, ZHAO Yanping, LI Chong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     luteolin
    ÏàËÆ¶È:53.3%
China Journal of Chinese Materia Medica          2008          33          1538-1540
Studies OR Chemical Constituents of Oxytropis Satcata
YANG Huan, WANG Dong, TONG Li, CAI Baochang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     5,7,3',4'-tetrahydroxyflavone
    ÏàËÆ¶È:53.3%
China Journal of Chinese Materia Medica          2006          31          391-395
Studies on flavonoids of Andrographis paniculata
CHENG Lixia, QU Gexia, QIU Feng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     luteolin
    ÏàËÆ¶È:53.3%
China Journal of Chinese Materia Medica          2005          30          444-446
Studies on chemical constituents in herb of Polygonum orientale
LI Yongjun, HE Xun, LIU Lina, LAN Yanyu, WANG Aimin, WANG Yonglin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     luteolin
    ÏàËÆ¶È:53.3%
China Journal of Chinese Materia Medica          2005          30          588-590
Studies on chemical constituents in herb of Chondrilla piptocoma
ZHAO Dongbao, YANG Yuxia, LIU Xiuhua, WANG Hanqing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     luteolin
    ÏàËÆ¶È:53.3%
China Journal of Chinese Materia Medica          2005          30          153-154
²ØÒ©¶ÌËëÍöú²Ý»¯Ñ§³É·ÖÑо¿
ÑîÔÆÉÑ, ºÎ Àó, Ñ÷, Ê·¸ß·å, ³Èó»ª
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     luteolin
C15H10O6     ÏàËÆ¶È:53.3%
China Journal of Chinese Materia Medica          2004          29          232-234
Studies on chemical constituents from herb of Dracocephalum moldavica
GU Haifeng, CHEN Ruoyun, SUN Yuhua, LIU Fa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     luteolin
C15H10O6     ÏàËÆ¶È:53.3%
China Journal of Chinese Materia Medica          1999          24         
Studies on Flavonoids from Aquilegia oxysepala Trautv. et Mey
Chen Sibao, Wang Liwei, Gao Guangyao, Liao Maochuan and Xiao Peigen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     luteolin
    ÏàËÆ¶È:53.3%
Fitoterapia          2009          80          461-464
A new biflavonoid from Daphniphyllum angustifolium Hutch
Mingfeng Xu , Lianqing Shen, Kuiwu Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     1,3-dihydroxy-5,6-dimethoxyxanthone
C15H12O6     ÏàËÆ¶È:53.3%
Journal of Natural Products          1988          Vol 51          339
Synthesis of 1,3-Dihydroxy-5,6-Dimethoxyxanthone, a Confirmation of Structure
S. Gil, M. Parra, V. Sanz, A. Tortajada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     chrysoeriol
C16H12O5     ÏàËÆ¶È:53.3%
Acta Pharmaceutica Sinica          2009          Vol 44          764−767
New homoisoflavanones from Polygonatum odoratum(Mill.) Druce
LI Li-hong; REN Feng-zhi; CHEN Shu-hong; GAO Yue-qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     chrysin
C15H10O4     ÏàËÆ¶È:53.3%
Acta Pharmaceutica Sinica          2005          Vol 40          351-354
Isolation and structure identification of chemical constituents from Viscum liquidambaricolum
YANG Yan-jun; LIN Jie-hong; XU Xiong-wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     luteolin
    ÏàËÆ¶È:53.3%
Natural Product Sciences          2001          7          72-75
Antioxidant Activity of Roasted Defatted Perilla Seed
Jung, Mee-Jung; Chung, Hae-Young; Choi, Jae-Sue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     1,6-dihydroxy-3,5-dimethoxyxanthone
    ÏàËÆ¶È:53.3%
Phytochemistry          1991          30          3625-3629
Xanthones fromChironia krebsii
Jean-luc Wolfender, Matthias Hamburger, Jerome D. Msonthi, Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     compound 4
    ÏàËÆ¶È:53.3%
Korean Journal of Pharmacognosy          1998          29(3)          209-216
Chemical Components of Rumex acetosella L.
Choe, Sang-Gil; Hwang, Bang-Yeon; Kim, Min-Su; Oh, Gap-Jin; Lee, Kyong-Soon; Ro, Jai-Seop
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     2'-hydroxygenistein
    ÏàËÆ¶È:53.3%
Phytochemistry          1987          26          295-300
Isoflavones from Lupinus angustifolius root
Geoffrey A. Lane,Roger H. Newman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
58 .     luteolin
    ÏàËÆ¶È:53.3%
Magnetic Resonance in Chemistry          2007          45          674-679
1H and 13C-NMR data of hydroxyflavone derivatives (pages 674¨C679)
Younghee Park, Byoung-Ho Moon, Eunjung Lee, Youngshim Lee, Youngdae Yoon, Joong-Hoon Ahn and Yoongho Lim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
59 .     Luteolin
    ÏàËÆ¶È:53.3%
Magnetic Resonance in Chemistry          2007          45          835-845
A predictive tool for assessing 13C NMR chemical shifts of flavonoids (pages 835¨C845)
Darcy C. Burns, David A. Ellis and Raymond E. March
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2013-03-27 08:28:20
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