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PSA: ½ð±Ò+1, 3u 2013-08-30 15:04:29
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1 ²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½1172¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ 7 . ɽéÙÖ¬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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

2Â¥2013-08-29 22:10:11
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ר¼Ò¾Ñé: +726 - PhEPI: 3
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PSA: ½ð±Ò+1, 3u 2013-08-30 15:04:38
PSA: ½ð±Ò+1, 3u 2013-08-30 15:04:38
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2 ²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½268¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

3Â¥2013-08-29 22:13:51
4Â¥2013-08-30 05:55:07














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