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bin85666666: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2012-11-05 21:32:27
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bin85666666: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2012-11-05 21:32:27
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ÕâÊÇÄãµÄ»¯ºÏÎïµÄÏàËÆ¶ÈÔÚ50%ÒÔÉÏµÄÆ¥ÅäÐÅÏ¢ ²éѯ½á¹û£º¹²²éµ½12¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . aversin C20H16O7 ÏàËÆ¶È:76.1% Magnetic Resonance in Chemistry 2007 45 434-438 1H and 13C NMR assignments for two anthraquinones and two xanthones from the mangrove fungus (ZSUH-36) (pages 434¨C438) Changlun Shao, Zhigang She, Zhiyong Guo, Hong Peng, Xiaoling Cai, Shining Zhou, Yucheng Gu and Yongcheng Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 6,8-dimethoxy-1-hydroxy-2-hydroxymethyl-3-methyl-9,10-anthraquinone ÏàËÆ¶È:66.6% Tetrahedron Letters 2005 46 2377-2380 An efficient regioselective synthesis of endocrocin and structural related natural anthraquinones starting from emodin Mario Waser, Bernd Lackner, Joachim Zuschrader, Norbert M¨¹ller, Heinz Falk Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (E)-7-methoxy-3-(4'-methoxybenzylidene)chroman-4-one C18H16O4 ÏàËÆ¶È:52.3% Chemical & Pharmaceutical Bulletin 2006 54(8) 1193-1195 Two New Homoisoflavonoids from Caesalpinia pulcherrima Muchchintala MAHESWARA, Vidavalur SIDDAIAH, and Chunduri VENKATA RAO Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 1-hydroxy-6,8-dimethoxy-3-methyl-9,10-anthraquinone-2-carboxylicacid ÏàËÆ¶È:52.3% Tetrahedron Letters 2005 46 2377-2380 An efficient regioselective synthesis of endocrocin and structural related natural anthraquinones starting from emodin Mario Waser, Bernd Lackner, Joachim Zuschrader, Norbert M¨¹ller, Heinz Falk Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . versicolorin B ÏàËÆ¶È:52.3% Chinese Journal of Medicinal Chemistry 2007 17 148-154 Anthraquinone derivatives produced by marine-derived Penicillium flavidorsum SHK1-27 and their antitumor activities REN Hong, GU Qian-qun, CUI Cheng-bin Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 7,10,11-trimethoxy-2H-2-azatriphenylene-1-one C20H17NO4 ÏàËÆ¶È:52.3% Bioorganic & Medicinal Chemistry 2008 16 6233-6241 Total synthesis of phenanthroindolizidine alkaloids (¡À)-antofine, (¡À)-deoxypergularinine, and their dehydro congeners and evaluation of their cytotoxic activity Chung-Ren Su, Amooru G. Damu, Po-Cheng Chiang, Kenneth F. Bastow, Susan L. Morris-Natschke, Kuo-Hsiung Lee, Tian-Shung Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . variecolorquinone A C20H18O9 ÏàËÆ¶È:52.3% The Journal of Antibiotics 2007 60 603-607 Two New Cytotoxic Quinone Type Compounds from the Halotolerant Fungus Aspergillus variecolor FREE Wenliang Wang, Tianjiao Zhu, Hongwen Tao, Zhenyu Lu, Yuchun Fang, Qianqun Gu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . versicolorin C C18H12O7 ÏàËÆ¶È:52.3% Chinese Journal of Organic Chemistry 2004 24 1114-1117 Anthraquinone Derivatives Isolated from Marine Fungus # 2526 from the South China Sea ZHU, Feng LIN, Yong-Cheng ZHOU, Shi-Ning Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 7 C25H24O12 ÏàËÆ¶È:52% Tetrahedron 2012 68 8480-8486 New mycotoxins from the scale insect fungus Aschersonia coffeae Henn. BCC 28712 Jittra Kornsakulkarn, Siriporn Saepua, Kitlada Srichomthong, Sumalee Supothina, Chawanee Thongpanchang Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . salcolin A ÏàËÆ¶È:50% Biochemical Systematics and Ecology 2010 38 656-658 Flavonolignans and other phenolic compounds from Sorghum halepense (L.) Pers. Hongjuan Huang, Yan Liu, Qinghui Meng, Shouhui Wei, Hailan Cui, Chaoxian Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 1-(4-fluorophenyl)-8-[(2-morpholin-4-ylisonicotinoyl)-amino]-4,5-dihydro-1H-benzo[g]indazole-3-carboxamide C28H27FN6O3 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2010 18 403-414 Aminopyridinecarboxamide-based inhibitors: Structure¨Cactivity relationship Dominique F. Bonafoux, Sheri L. Bonar, Michael Clare, Ann M. Donnelly, Jeanette L. Glaenzer, Julia A. Guzova, He Huang, Nandidni N. Kishore, Francis J. Koszyk, Patrick J. Lennon, Adam Libby, Sumathy Mathialagan, David S. Oburn, Sharon A Rouw, Cynthia D. S Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (3Z,6Z)-3-((5-tert-butyl-1H-imidazol-4-yl)methylene)-6-(3-(2,4-dimethoxybenzoyl)benzylidene)piperazine-2,5-dione C28H28N4O5 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2012 20 4279-4289 Synthesis and structure¨Cactivity relationships of benzophenone-bearing diketopiperazine-type anti-microtubule agents Yuri Yamazaki, Makiko Sumikura, Yurika Masuda, Yoshiki Hayashi, Hiroyuki Yasui, Yoshiaki Kiso, Takumi Chinen, Takeo Usui, Fumika Yakushiji, Barbara Potts, Saskia Neuteboom, Michael Palladino, George Kenneth Lloyd, Yoshio Hayashi Structure 13C NMR ̼Æ×Ä£Äâͼ |
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