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liangtingmei: ½ð±Ò+11, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2015-04-15 19:40:52
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liangtingmei: ½ð±Ò+11, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2015-04-15 19:40:52
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²éѯ½á¹û£º¹²²éµ½159¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Pachybasin ÏàËÆ¶È:100% Archives of Pharmacal Research 2012 35 461-468 Tetrahydroanthraquinone and Xanthone Derivatives from the Marine-Derived Fungus Trichoderma aureoviride PSU-F95 Nanthaphong Khamthong,Vatcharin Rukachaisirikul,Kwanruthai Tadpetch,Morakot Kaewpet,Souwalak Phongpaichit,Sita Preedanon,and Jariya Sakayaroj Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Pachybasin ÏàËÆ¶È:100% Chirality 2013 25 141-148 Structural and Stereochemical Studies of Hydroxyanthraquinone Derivatives from the Endophytic Fungus Coniothyrium sp Peng Sun, Juan Huo, Tibor Kurt¨¢n, Attila M¨¢ndi, S¨¢ndor Antus, Hua Tang, Siegfried Draeger, Barbara Schulz, Hidayat Hussain, Karsten Krohn, Weihua Pan, Yanghua Yi and Wen Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . Pachybasin ÏàËÆ¶È:100% Chirality 2013 25 141-148 Structural and Stereochemical Studies of Hydroxyanthraquinone Derivatives from the Endophytic Fungus Coniothyrium sp (pages 141¨C148) Peng Sun, Juan Huo, Tibor Kurt¨¢n, Attila M¨¢ndi, S¨¢ndor Antus, Hua Tang, Siegfried Draeger, Barbara Schulz, Hidayat Hussain, Karsten Krohn, Weihua Pan, Yanghua Yi and Wen Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 1-hydroxy-6-Methyl-9,10-anthraquinone ÏàËÆ¶È:93.3% Natural Product Research and Development 2014 26 159-161 A New Compound from Trichoderma sp. KK19L1 YU He, WANG Xiang-fen, JI Yan-nan, XU Yan, TIAN Sha-sha, ZHU Hua-jie* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 1-Hydroxy-3-methoxyanthraquinone ÏàËÆ¶È:80% Archives of Pharmacal Research 2012 35 461-468 Tetrahydroanthraquinone and Xanthone Derivatives from the Marine-Derived Fungus Trichoderma aureoviride PSU-F95 Nanthaphong Khamthong,Vatcharin Rukachaisirikul,Kwanruthai Tadpetch,Morakot Kaewpet,Souwalak Phongpaichit,Sita Preedanon,and Jariya Sakayaroj Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . anthraquinones chrysophanol C15H10O4 ÏàËÆ¶È:73.3% Acta Botanica Sinica 2003 45 1003-1007 Two New Triterpenes from Neonauclea sessilifolia KANG Wen-Yi, LI Guo-Hong, HAO Xiao-Jiang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 1-hydroxy-anthraquinone C14H8O3 ÏàËÆ¶È:73.3% Acta Pharmaceutica Sinica 1992 27 358-364 ANTHRAQUINONES ISOLATED FROM MORINDA OFFICINALIS AND DAMNACANTHUS INDICUS YJ Yang; HY Shu; ZD Min Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 1-hydroxyanthraquinone ÏàËÆ¶È:73.3% Natural Product Sciences 2002 8 48-51 Antioxidant Activity of Anthraquinones from Morinda elliptica Ismail, Nor Hadiani; Mohamad, Habsah; Mohidin, Amran; Lajis, Nordin Hj. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . Pachybasin,1-hydroxy-3-methyl-9,10-anthraquinone ÏàËÆ¶È:73.3% Journal of the Brazilian Chemical Society 2006 17 929-934 Novel Anthraquinone Derivatives Produced by Phoma sorghina, an Endophyte Found in Association with the Medicinal Plant Tithonia diversifolia (Asteraceae) Warley de Souza Borges and Mônica Tallarico Pupo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . Ýìõ«´ó»Æ·Ó ÏàËÆ¶È:73.3% Journal of Chinese Medicinal Materials 2002 25 875-877 Study on the Constituents from Neonauclea sessilifolia Kang Wenyi, Hao Xiaojiang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 2-hydroxy-9,10-anthraquinone ÏàËÆ¶È:73.3% Organic Magnetic Resonance 1978 11 375-377 The carbon-13 nuclear magnetic resonance spectra of anthraquinone, eight polyhydroxyanthraquinones and eight polymethoxyanthraquinones Y. Berger and A. Castonguay Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 2-ethyl-1(3)H-anthra[1,2-d]imidazole-6,11-dione C17H12N2O2 ÏàËÆ¶È:70.5% Bioorganic & Medicinal Chemistry 2009 17 7418-7428 Synthesis, cytotoxicity and human telomerase inhibition activities of a series of 1,2-heteroannelated anthraquinones and anthra[1,2-d]imidazole-6,11-dione homologues Hsu-Shan Huang, Tsung-Chih Chen, Ruei-Huei Chen, Kuo-Feng Huang, Fong-Chun Huang, Jing-Ru Jhan, Chun-Liang Chen, Chia-Chung Lee, Yang Lo, Jing-Jer Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 1-hydroxy-2-hydroxymethy-3-methoxyanthraquinine ÏàËÆ¶È:68.7% Journal of Shenyang Pharmaceutical University 2009 26 904-906 Chemical constituents from whole plant of Galiun verum L. ZHAO Chun-chao, SHAO Jian-hua, ZHANG Yu-wei, CAO Dan-dan, LI Xian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 11-methyl-6H-isoindolo[2,1-a]indol-6-one C16H11NO ÏàËÆ¶È:68.7% Tetrahedron 2012 68 3112-3116 Synthesis of 6H-isoindolo[2,1-a]indol-6-ones through a sequential copper-catalyzed C-N coupling and palladium-catalyzed C¨CH activation reaction Hua-Feng He, Sheng Dong, Yi Chen, Yang Yang, Yueqin Le, Weiliang Bao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . barleriaquinone C15H10O3 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1984 32 4137-4139 Chemical Examination of the Roots of Barleria buxifolia LINN. Structure of Barleriaquinone SUBBARAYAN GOPALAKRISHNAN,STHANUSUBRAMANIA NEELAKANTAN,PATHAI VENKATESWARA RAMAN,TORU OKUYAMA and SHOJI SHIBATA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 1-hydroxy-2-methylanthraquinone C15H10O3 ÏàËÆ¶È:66.6% Acta Pharmaceutica Sinica 1992 27 358-364 ANTHRAQUINONES ISOLATED FROM MORINDA OFFICINALIS AND DAMNACANTHUS INDICUS YJ Yang; HY Shu; ZD Min Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 6-(3,4-dichlorophenyl)-2-(4-methoxyphenyl)-4,5-dihydro-3(2H)-pyridazinone C17H14Cl2N2O2 ÏàËÆ¶È:66.6% Journal of Heterocyclic Chemistry 2005 42 131-135 A general and facile synthesis of 1,3-diaryl-4-pyrazoleacetic acid esters David D. Xu,George T. Lee,Xinglong Jiang,Kapa Prasad,Oljan Repic and Thomas J. Blacklock Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . o-[N-(2-thiothenoyl)amino]benzyl 2-thiophencarboxylate C17H13NO2S3 ÏàËÆ¶È:66.6% Heterocycles 2002 58 203-212 Sulfur-containing Heterocycles Derived by Reaction of N-Thioacylamino Alcohols with Lawesson's Reagent and Saponification of N-Thioacylamino Esters Takehiko Nishio* and Hiroshi Sekiguchi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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