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1 . Janthinone ÏàËÆ¶È:100% Marine Drugs 2012 10 559-582 Activation of the Dormant Secondary Metabolite Production by Introducing Gentamicin-Resistance in a Marine-Derived Penicillium purpurogenum G59 Yun-Jing Chai,Cheng-Bin Cui ,Chang-Wei Li,Chang-Jing Wu,Cong-Kui Tian and Wei Hua Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Methyl 8-hydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylate C16H12O5 ÏàËÆ¶È:100% Magnetic Resonance in Chemistry 2008 46 1066-1069 Structure elucidation of two new xanthone derivatives from the marine fungus Penicillium sp. (ZZF 32#) from the South China Sea (pages 1066¨C1069) Changlun Shao, Changyun Wang, Meiyan Wei, Yucheng Gu, Xuekui Xia, Zhigang She and Yongcheng Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 11-hydroxy-1-methoxycarbonyl-9-methylxanthone C16H12O5 ÏàËÆ¶È:100% European Journal of Organic Chemistry 2008 2008 698-703 Isofusidienols: Novel Chromone-3-oxepines Produced by the Endophytic Fungus Chalara sp. Sandra Lösgen, Jörg Magull, Barbara Schulz, Siegfried Draeger and Axel Zeeck Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 8-hydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylic acid methyl ester ÏàËÆ¶È:94.1% Phytochemistry 2001 58 751-758 Phytotoxic naphthopyranone derivatives from the coprophilous fungus Guanomyces polythrix Martha Mac¨ªas, Alicia Gamboa, Miguel Ulloa, Rub¨¦n A. Toscano, Rachel Mata Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . janthinone C16H12O5 ÏàËÆ¶È:87.5% Natural Product Communications 2009 4 1481-1483 Secondary Metabolites from the Mangrove EndophyticFungus Penicillium sp. (SBE-8) Zhiyong Guo, Fan Cheng, Kun Zou, Junzhi Wang, Zhigang She, and Yongcheng Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . vertixanthone C15H10O5 ÏàËÆ¶È:81.2% Journal of Natural Products 1989 Vol 52 119 Metabolites of Leptographium wageneri, the Causative Agent of Black Stain Root Disease of Conifers William A. Ayer, Lois M. Browne, Ge Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 7-hydroxyjanthinone C16H12O6 ÏàËÆ¶È:81.2% Natural Product Communications 2009 4 1481-1483 Secondary Metabolites from the Mangrove EndophyticFungus Penicillium sp. (SBE-8) Zhiyong Guo, Fan Cheng, Kun Zou, Junzhi Wang, Zhigang She, and Yongcheng Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 1-Hydroxy-10-methoxy-dibenz[b,e]oxepin-6,11-dione C15H10O5 ÏàËÆ¶È:81.2% Marine Drugs 2012 10 2691-2697 A New Dibenz[b,e]oxepine Derivative, 1-Hydroxy-10-methoxy-dibenz[b,e]oxepin-6,11-dione, from a Marine-Derived Fungus, Beauveria bassiana TPU942 Hiroyuki Yamazaki, Henki Rotinsulu, Tsuyoshi Kaneko, Kazuki Murakami, Hiromu Fujiwara, Kazuyo Ukai and Michio Namikoshi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 1-hydroxy-3-methylxanthone ÏàËÆ¶È:75% Chemical & Pharmaceutical Bulletin 1998 46 1506-1510 Manoamine Oxidase Inhibitory constituents from Anixiella micropertusa Haruhiro FUJIMOTO,Yoko SATOH,Kentaro YAMAGUCHI and Mikio YAMAZAKI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . Sydowinin A C16O6H12 ÏàËÆ¶È:75% Journal of Agricultural and Food Chemistry 2014 62 8602−8607 Differential Production of Phytotoxins from Phomopsis sp. From Grapevine Plants Showing Esca Symptoms Mary-Lorène Goddard, Nicolas Mottier, Julie Jeanneret-Gris, Danilo Christen, Raphaël Tabacchi, and Eliane Abou-Mansour Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . Microsxanthone C16H12O6 ÏàËÆ¶È:75% Chemistry-A European Journal 2009 15 12121-12132 Xanthones and Oxepino[2, 3-b]chromones from Three Endophytic Fungi Karsten Krohn, Simeon F. Kouam, Guy M. Kuigoua, Hidayat Hussain, Stephan Cludius-Brandt, Ulrich Flörke, Tibor Kurt¨¢n, Gennaro Pescitelli, Lorenzo Di Bari, Siegfried Draeger and Barbara Schulz Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . Alternethanoxin B C16H12O6 ÏàËÆ¶È:75% Journal of Agricultural and Food Chemistry 2009 57 6656-6660 Alternethanoxins A and B, Polycyclic Ethanones Produced by Alternaria sonchi, Potential Mycoherbicides for Sonchus arvensis Biocontrol Antonio Evidente, Biancavaleria Punzo, Anna Andolfi, Alexander Berestetskiy and Andrea Motta Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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