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΢Æ×ÇóÖú£¬ÔÚÏߵȣ¡ ÒÑÓÐ1È˲ÎÓë
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| 13C NMR (151 MHz, DMSO) ¦Ä25.27, 26.28, 26.41, 49.07, 70.51, 89.02, 91.99, 103.10, 105.89, 106.68, 108.99, 109.56, 120.86, 132.67, 155.83, 156.46, 156.85, 158.02, 159.06, 166.63, 181.12. |
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²éѯ½á¹û£º¹²²éµ½34¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . erythrinin C ÏàËÆ¶È:66.6% Natural Product Research and Development 2012 24 610-613 Isoflavonoids from Piptanthus concolor Harrow KOU Zhong-jing; CHANG Rui-jie; QIN Jiang-jiang; YAN Shi-kai; JIN Hui-zi; ZHANG Wei-dong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 1,7-dihydroxy-2,3-[2''-(1-hydroxy-1-methylethyl)-dihydrofurano]-xanthone C18H16O6 ÏàËÆ¶È:61.9% Phytochemistry 2006 67 2146-2151 Xanthones from Hypericum chinense Naonobu Tanaka, Yoshihisa Takaishi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (1''R)-5,4',1''-trihydroxy-6,7-(3'',3''-dimethylchroman)flavone C20H18O6 ÏàËÆ¶È:61.9% Journal of Natural Products 2006 69 1687-1691 Antihyperglycemic Activity and Chemical Constituents of Eysenhardtia platycarpa Jos M. Narvez-Mastache, Mara Luisa Garduo-Ramrez, Laura Alvarez, and Guillermo Delgado Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . prim-O-glucosylangelicain C21H26O11 ÏàËÆ¶È:61.9% Chemical & Pharmaceutical Bulletin 1983 31 64-69 Chemical Studies of Coelopleurum gmelinii (D.C.) LEDEB. I. Constituents of the Root MITSUGI KOZAWA,YOUKO MATSUYAMA,MASAYO FUKUMOTO and KIMIYE BABA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 7-O-methylluteone C21H20O6 ÏàËÆ¶È:57.1% Phytochemistry 2003 445-448 Two prenylated flavonoids from the stem bark of Erythrina burttii Abiy Yenesew, Beatrice Irungu, Solomon Derese, Jacob O. Midiwo,Matthias Heydenreich, Martin G. Peter Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . licofuranocoumarin C21H20O7 ÏàËÆ¶È:57.1% Phytochemistry 2000 55 959-963 Minor flavonoids from licorice Tsutomu Hatano, Yasuhiro Ag, Yasushi Shintani, Hideyuki Ito, Takuo Okuda, Takashi Yoshida Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . isolicopyranocoumarin C21H20O7 ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 1997 45 1485-1492 Phenolic Constituents of Liquorice. VII. A New Chalcone with a Potent Radical Scavenging Activity and Accompanying Phenolics from Liquorice Tsutomu HATANO,Miyuki TAKAGI,Hideyuki ITO and Takashi YOSHIDA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 2'-hydroxygenistein 7-O-glucopyranoside ÏàËÆ¶È:57.1% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . prim-O-glucosylangelicain ÏàËÆ¶È:57.1% Journal of Asian Natural Products Research 2005 7 145-149 Chemical constituents from Cimicifuga foetida PEI CAO, XU-FENG PU, SHU-LIN PENG, XIAO-RONG ZHANG and LI-SHENG DING Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . cajanin C16H12O6 ÏàËÆ¶È:57.1% Phytochemistry 2000 53 981-985 Indicanines B and C, two isoflavonoid derivatives from the root bark of Erythrina indica Alain K. Waffo, Guy A. Azebaze, Augustin E. Nkengfack, Zacharias T. Fomum, Michele Meyer, Bernard Bodo, Fanie R. van Heerden Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . luteone ÏàËÆ¶È:57.1% Phytochemistry 1987 26 295-300 Isoflavones from Lupinus angustifolius root Geoffrey A. Lane,Roger H. Newman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . mangoxanthone C23H24O6 ÏàËÆ¶È:56.5% Phytochemistry 2005 66 1718-1723 Xanthones and benzophenones from Garcinia griffithii and Garcinia mangostana Nilar, Lien-Hoa D. Nguyen, Ganpathi Venkatraman, Keng-Yeow Sim, Leslie J. Harrison Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . lupinisoflavone G ÏàËÆ¶È:56% Phytochemistry 1999 52 87-94 Six diprenylisoflavones, derrisisoflavones A-F, from Derris scandens Toshikazu Sekine, Miyuki Inagaki, Fumio Ikegami, Yuichi Fujii, Nijsiri Ruangrungsi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . kanzonol N C22H24O6 ÏàËÆ¶È:54.5% Heterocycles 1994 38 1089-1098 Five New Isoprenoid-substituted Flavonoids, Kanzonols M - P and R, from Two Glycyrrhiza Species Toshio Fukai, Junko Nishizawa, Masami Yokoyama, Liming Tantai, and Taro Nomura Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 5,2',4'-trihydroxy-7-methoxy-5'-(3-methylbuten-2-yl)isoflavone C21H20O6 ÏàËÆ¶È:52.3% Journal of Natural Products 2009 72 1603-1607 Isoflavonoids from Erythrina poeppigiana: Evaluation of Their Binding Affinity for the Estrogen Receptor Sefirin Djiogue, Maria Halabalaki, Xanthippi Alexi, Dieudonne Njamen, Zacharias Tanee Fomum, Michael N. Alexis, and Alexios-Leandros Skaltsounis Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . eriophorin B C18H16O6 ÏàËÆ¶È:52.3% Journal of Natural Products 2005 68 1094-1098 Flavonoids from the Stem of Eriophorum scheuchzeri Milena Maver, Emerson F. Queiroz, Jean-Luc Wolfender, and Kurt Hostettmann Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . vismiaguianin B C20H20O6 ÏàËÆ¶È:52.3% Phytochemistry 2000 55 35-42 New bioactive aromatic compounds from Vismia guianensis Eun-Kyoung Seo, Mansukh C. Wani, Monroe E. Wall, Hernan Navarro, Rabindranath Mukherjee, Norman R. Farnsworth, A. Douglas Kinghorn Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . erystagallin C C20H20O5 ÏàËÆ¶È:52.3% Phytochemistry 1997 45 835-838 Three pterocarpans from Erythrina crista-galli Hitoshi Tanaka, Toshihiro Tanaka, Hideo Etoh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . phaseollidin ÏàËÆ¶È:52.3% Phytochemistry 1994 36 1047-1051 Prenylated isoflavanone from the roots of Erythrina sigmoidea Augustin E. Nkengfack, Timothee W. Vouffo, Z.T. Fomum, Michele Meyer, Ola Bergendorff, Olov Sterner Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . lyratin A C20H22O5 ÏàËÆ¶È:52.3% Chemical & Pharmaceutical Bulletin 2010 58 840-842 New Anti-inflammatory 4-Hydroxyisoflavans from Solanum lyratum De-Wu Zhang, Gui-Hai Li, Qun-Ying Yu and Sheng-Jun Dai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-02-21 12:50:13
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|
²éѯ½á¹û£º¹²²éµ½51¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . erythrinin C ÏàËÆ¶È:68.4% Natural Product Research and Development 2012 24 610-613 Isoflavonoids from Piptanthus concolor Harrow KOU Zhong-jing; CHANG Rui-jie; QIN Jiang-jiang; YAN Shi-kai; JIN Hui-zi; ZHANG Wei-dong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 1,7-dihydroxy-2,3-[2''-(1-hydroxy-1-methylethyl)-dihydrofurano]-xanthone C18H16O6 ÏàËÆ¶È:63.1% Phytochemistry 2006 67 2146-2151 Xanthones from Hypericum chinense Naonobu Tanaka, Yoshihisa Takaishi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . cajanin C16H12O6 ÏàËÆ¶È:63.1% Phytochemistry 2000 53 981-985 Indicanines B and C, two isoflavonoid derivatives from the root bark of Erythrina indica Alain K. Waffo, Guy A. Azebaze, Augustin E. Nkengfack, Zacharias T. Fomum, Michele Meyer, Bernard Bodo, Fanie R. van Heerden Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . (1''R)-5,4',1''-trihydroxy-6,7-(3'',3''-dimethylchroman)flavone C20H18O6 ÏàËÆ¶È:60% Journal of Natural Products 2006 69 1687-1691 Antihyperglycemic Activity and Chemical Constituents of Eysenhardtia platycarpa Jos M. Narvez-Mastache, Mara Luisa Garduo-Ramrez, Laura Alvarez, and Guillermo Delgado Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . luteone ÏàËÆ¶È:60% Phytochemistry 1987 26 295-300 Isoflavones from Lupinus angustifolius root Geoffrey A. Lane,Roger H. Newman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . eriophorin B C18H16O6 ÏàËÆ¶È:57.8% Journal of Natural Products 2005 68 1094-1098 Flavonoids from the Stem of Eriophorum scheuchzeri Milena Maver, Emerson F. Queiroz, Jean-Luc Wolfender, and Kurt Hostettmann Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . parvisoflavone A ÏàËÆ¶È:57.8% Heterocycles 2008 75 3085-3089 Studies of the Egyptian Traditional Folk Medicines. IV. New Isoflavonoid Isolated from Egyptian Licorice Masaki Baba, Sakiko Sumi, Noriaki Iwasaki, Hisahiro Kai, Masami Sakano (nee Komiya), Yoshihito Okada, and Toru Okuyama Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 7-O-methylluteone C21H20O6 ÏàËÆ¶È:57.1% Phytochemistry 2003 445-448 Two prenylated flavonoids from the stem bark of Erythrina burttii Abiy Yenesew, Beatrice Irungu, Solomon Derese, Jacob O. Midiwo,Matthias Heydenreich, Martin G. Peter Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . licofuranocoumarin C21H20O7 ÏàËÆ¶È:57.1% Phytochemistry 2000 55 959-963 Minor flavonoids from licorice Tsutomu Hatano, Yasuhiro Ag, Yasushi Shintani, Hideyuki Ito, Takuo Okuda, Takashi Yoshida Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . isolicopyranocoumarin C21H20O7 ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 1997 45 1485-1492 Phenolic Constituents of Liquorice. VII. A New Chalcone with a Potent Radical Scavenging Activity and Accompanying Phenolics from Liquorice Tsutomu HATANO,Miyuki TAKAGI,Hideyuki ITO and Takashi YOSHIDA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 2'-hydroxygenistein 7-O-glucopyranoside ÏàËÆ¶È:57.1% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . prim-O-glucosylangelicain C21H26O11 ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 1983 31 64-69 Chemical Studies of Coelopleurum gmelinii (D.C.) LEDEB. I. Constituents of the Root MITSUGI KOZAWA,YOUKO MATSUYAMA,MASAYO FUKUMOTO and KIMIYE BABA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . erystagallin C C20H20O5 ÏàËÆ¶È:55% Phytochemistry 1997 45 835-838 Three pterocarpans from Erythrina crista-galli Hitoshi Tanaka, Toshihiro Tanaka, Hideo Etoh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . phaseollidin ÏàËÆ¶È:55% Phytochemistry 1994 36 1047-1051 Prenylated isoflavanone from the roots of Erythrina sigmoidea Augustin E. Nkengfack, Timothee W. Vouffo, Z.T. Fomum, Michele Meyer, Ola Bergendorff, Olov Sterner Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . lyratin A C20H22O5 ÏàËÆ¶È:55% Chemical & Pharmaceutical Bulletin 2010 58 840-842 New Anti-inflammatory 4-Hydroxyisoflavans from Solanum lyratum De-Wu Zhang, Gui-Hai Li, Qun-Ying Yu and Sheng-Jun Dai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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4Â¥2014-02-21 13:48:16
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5Â¥2014-02-21 14:38:55














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