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zemezh: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2014-04-29 19:53:46
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zemezh: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2014-04-29 19:53:46
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²éѯ½á¹û£º¹²²éµ½93¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 3-Methoxyangelicin C12H18O4 ÏàËÆ¶È:58.3% Phytochemistry 1993 34 585-586 3-Methoxyfurocoumarins from Pilocarpus riedelianus Adolfo H. M¨¹ller, Luis R.O. Deg¨¢spari, Paulo C. Vieira, M. Fatima Das G.F. da Silva, João B. Fernandes, Jos¨¦ R. Pirani Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 2-amino-1,8-dihydro-7-methoxy-1-methyl-8-oxopyrrolo[4,3,2-de]quinoline C12H11N3O2 ÏàËÆ¶È:58.3% European Journal of Organic Chemistry 1999 1999 1173-1183 Syntheses of Batzelline A, Batzeline B, Isobatzelline A, and Isobatzelline B Mercedes Alvarez, M. Antonieta Bros, Gemma Gras, Wadi Ajana and John A. Joule Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 6,7-dimethoxyquinazolin-4(3H)-one ÏàËÆ¶È:58.3% Bioorganic & Medicinal Chemistry 2013 21 7858-7873 Investigation of quinazolines as inhibitors of breast cancer resistance protein (ABCG2) Kapil Juvale, Jennifer Gallus, Michael Wiese Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 6,8-Dimethoxy-3-methylisocoumarin C12H12O4 ÏàËÆ¶È:58.3% Natural Product Communications 2011 6 45-48 Bioactive Isocoumarins from a Terrestrial Streptomyces sp. ANK302 Dhafer Saber Zinad, Khaled A. Shaaban, Muna Ali Abdalla, Md. Tofazzal Islam, Anja Sch¨¹ffler and Hartmut Laatsch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . ɽÄÎËØ-4'-¼×ÃÑ ÏàËÆ¶È:58.3% Journal of Tropical and Subtropical Botany 2000 8 182-184 ºì¶¹É¼(Taxus chinensis(Pilger) Rehd.)ÖеķÇ×ÏɼÍéÀ໯ºÏÎï ¹ÙÖÇ, ËÕ¾µÓé, ÔøÂ¤Ã·, Àîºì Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 6,8-Dimethoxy-3-methylisocoumarin ÏàËÆ¶È:58.3% The Journal of Organic Chemistry 1989 54 4218-4220 An improved synthesis of 6,8-dimethoxy-3-methylisocoumarin, a fungal metabolite precursor J. Kirby Kendall, Thomas H. Fisher, Harry P. Schultz, Tor P. Schultz Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . evolitrie C13H11NO3 ÏàËÆ¶È:53.8% Chinese Traditional and Herbal Drugs 2010 41 1052-1056 Chemical constituents from stems of Melicope pteleifolia LI Shuo-guo; YANG Yin; YE Wen-cai; JIANG Ren-wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . cordifoliketone B C13H16O6 ÏàËÆ¶È:53.8% Bulletin of the Korean Chemical Society 2012 33 278-280 Phenylpropanoids from the Roots of Codonopsis cordifolioidea and Their Biological Activities Qiufen Hu,*, Xuesen Li, Haitao Huang, Huaixue Mu, Penfei Tu, Ganpeng Li*, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 1,3,5-trihydroxy-6,7-dimethoxyxanthone ÏàËÆ¶È:53.3% Phytochemistry 2006 67 2146-2151 Xanthones from Hypericum chinense Naonobu Tanaka, Yoshihisa Takaishi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 5,6,7-Trimethoxydictamnine C15H15NO5 ÏàËÆ¶È:53.3% Natural Product Communications 2006 1 351-356 Novel Metabolites from the Stem Bark of Brombya sp. nova(Gap Creek) (Rutaceae) Clynton W. Halstead, Paul I. Forster and Peter G. Waterman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . methyl (2E)-3-(7-methoxy-1,3-benzodioxol-5-yl)prop-2-enoate C12H12O5 ÏàËÆ¶È:50% Helvetica Chimica Acta 2007 Vol. 90 2222 A Novel Norlignan and a Novel Phenylpropanoid from Peperomia tetraphylla Yun-Zhi Li, Jing Huang, Zhen Gong, and Xiang-Qing Tian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . sodium aristolochate IVa ÏàËÆ¶È:50% Phytochemistry 2003 63 953-957 Diterpene esters of aristolochic acids from Aristolochia pubescens Isabele R. Nascimento, Lucia M.X. Lopes Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . (2R,3R)-2,3-bis(5-methoxy-3,4-methylenedioxybenzyl)butane-1,4-diol C22H26O8 ÏàËÆ¶È:50% Journal of Natural Products 2006 69(2) 234-239 Bioactive Dibenzylbutyrolactone and Dibenzylbutanediol Lignans from Peperomia duclouxii Na Li, Jian-lin Wu, Toshiaki Hasegawa, Jun-ichi Sakai, Li-yan Wang, Saori Kakuta, Yumiko Furuya, Akihiro Tomida, Takashi Tsuruo, and Masayoshi Ando Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . benzyl 2-hydroxy-3,6-dimethoxybenzoate C16H16O5 ÏàËÆ¶È:50% Journal of Natural Products 2002 65 1165-1167 Four New Compounds from the Seeds of Cassia fistula Yueh-Hsiung Kuo, Ping-Hung Lee, and Yung-Shun Wein Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . N-(2-hydroxy-4,5-dimethoxyphenyl)-(S)-¦Á-malamic acid C12H15NO7 ÏàËÆ¶È:50% Journal of Natural Products 1998 61 1174-1176 Isolation and Synthesis of an ¦Á-Malamic Acid Derivative from Justicia ghiesbreghtiana Lotfy D. Ismail, Peter Lorenz, and Frank R. Stermitz Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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