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. sulochrin C17H16O7 ÏàËÆ¶È:80% Journal of Natural Products 2002 65 7-10 New Chlorinated Diphenyl Ethers from an Aspergillus Species Jaih Hargreaves, Ja-on Park, Emilio L. Ghisalberti, Krishnapillai Sivasithamparam, Brian W. Skelton, and Allan H. White Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Sulochrin C17H16O7 ÏàËÆ¶È:80% Bioscience, Biotechnology, and Biochemistry 2003 67 442-444 Hydroxysulochrin, a Tea Pollen Growth Inhibitor from the Fungus Aureobasidium sp. Atsumi SHIMADA, Chisako SHIOKAWA, Miyako KUSANO, Shozo FUJIOKA and Yasuo KIMURA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . sulochrin C17H16O7 ÏàËÆ¶È:80% The Journal of Antibiotics 2002 55 552-556 Fungal Metabolites, Asterric Acid Derivatives Inhibit Vascular Endothelial Growth Factor (VEGF)-induced Tube Formation of HUVECs HEE JUNG LEE,JEONG HYEONG LEE,BANG YEON HWANG,HANG SUB KIM and JUNG JOON LEE Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . sulochrin ÏàËÆ¶È:80% The Journal of Antibiotics 1997 50 972-974 Sulochrin Inhibits Eosinophil Degranulation HIROSHI OHASHI, MASAHARU ISHIKAWA, JUNKO ITO, AKIHIRO UENO, GERALD J. GLEICH, HIROHITO KITA, HIROYUKI KAWAI, HIROMI FUKAMACHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . Hydroxysulochrin C17H16O8 ÏàËÆ¶È:73.3% Bioscience, Biotechnology, and Biochemistry 2003 67 442-444 Hydroxysulochrin, a Tea Pollen Growth Inhibitor from the Fungus Aureobasidium sp. Atsumi SHIMADA, Chisako SHIOKAWA, Miyako KUSANO, Shozo FUJIOKA and Yasuo KIMURA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . methyl 6-acetyl-4-methoxy-5,7,8-trihydroxynaphthalene-2-carboxylate ÏàËÆ¶È:73.3% Electronic Journal of Biotechnology 2009 12 1-9 Novel antimicrobial secondary metabolites from a Penicillium sp. isolated from Brazilian cerrado soil Philippe Petit,Esther M. F. Lucas,Lucas M. Abreu,Ludwig H. Pfenning,Jacqueline A. Takahashi* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . methyl 2-(2-formyl-3-hydroxy-5-methylphenoxy)-5-hydroxy-3-methoxybenzoate C17H16O7 ÏàËÆ¶È:70.5% Natural Product Research 2012 26 1224-1228 A new diphenyl ether from Phoma sp. strain, SHZK-2 M.J. Fang, H. Fang, W.J. Li, D.M. Huang, Z. Wu & Y.F. Zhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . Sulochrin C17H16O7 ÏàËÆ¶È:66.6% Russian Chemical Bulletin 2011 60 760-763 4-Methoxy-3-methylgoniothalamin from marine-derived fungi of the genus Penicillium O. F. Smetanina, A. N. Yurchenko, A. I. Kalinovsky, M. A. Pushilin and N. N. Slinkina, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 1,2-seco-trypacidin ÏàËÆ¶È:61.1% Chinese Journal of Natural Medicines 2005 3 269-271 Secondary Metabolites of Aspergillus fumigatus var. fumigatus LU Chun-Hua; HUANG Yao-Jian; SHEN Yue-Mao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . monomethylsulochrin ÏàËÆ¶È:61.1% The Journal of Antibiotics 2006 59 362-365 A New Diphenyl Ether from Marine-derived Fungus Aspergillus sp. B-F-2 FREE Rui Liu, Weiming Zhu, Yapeng Zhang, Tianjiao Zhu, Hongbing Liu, Yuchun Fang and Qianqun Gu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 6-methyl-anthragallol-2-methyl ether C16H12O5 ÏàËÆ¶È:56.2% Natural Product Sciences 2004 10 63-68 Anthraquinones with Antibacterial Activities from Crucianella maritima L. Growing in Egypt El-Lakany, Abdalla M.; Aboul-Ela, Maha A.; Abdel-Kader, Maged S.; Badr, Jihan M.; Sabri, Nawal N.; Goher, Yousry Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 2-(2,6-dihydroxy-4-methoxybenzoyl)-3,5-dimethoxybenzoic acid ÏàËÆ¶È:56.2% Helvetica Chimica Acta 2013 96 458-462 Two New Secoanthraquinone Derivatives from the Marine-Derived Endophytic Fungus Aspergillus wentii EN-48 Hao-Fen Sun, Xiao-Ming Li, Ling-Hong Meng, Chuan-Ming Cui, Shu-Shan Gao, Chun-Shun Li and Bin-Gui Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 1,4,5-trihydroxy-7-methoxy-2-methyl-anthraquinone ÏàËÆ¶È:56.2% Phytotherapy Research 2014 28 774−780 Anti-leishmanial Activities of Extracts and Isolated Compounds from Drechslera rostrata and Eurotium tonpholium Amani S. Awaad, Haifa M. Al-Zaylaee, Saleh I. Alqasoumi, Mohamed E. Zain, Ebtesam M. Aloyan, Ahmed M. Alafeefy, Elham S. H. Awad and Reham M. El-Meligy Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . methyl asterrate C18H18O8 ÏàËÆ¶È:55.5% Natural Product Research 2012 26 1224-1228 A new diphenyl ether from Phoma sp. strain, SHZK-2 M.J. Fang, H. Fang, W.J. Li, D.M. Huang, Z. Wu & Y.F. Zhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . monom ethyl sulochrin C18H18O7 ÏàËÆ¶È:55.5% Chinese Journal of New Drugs 2010 19 1402-1406 Identification of endophytic fungi SIPI3.0550 and its metabolites ZHANG Zhi-jie, QU Ling-bo, ZHOU Yu-meng, LI Ji-an, SHAO Lei, CHEN Dai-jie Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . monomethylsulochrin ÏàËÆ¶È:55.5% Chemistry of Natural Compounds 2014 50 526-528 Antimicrobial Metabolites from the Endophytic Fungus Aspergillus sp. of Eucommia ulmoides Hongchi Zhang, Rui Liu, Feng Zhou, Runmei Wang, Xiaocui Liu, Hangtao Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 6-hydroxymethyleugenin ÏàËÆ¶È:53.3% Journal of Natural Products 2002 65 1681-1682 The Isolation of Two New Chromone Derivatives from the New Zealand Fungus Tolypocladium extinguens Yunjiang Feng, John W. Blunt, Anthony L. J. Cole, and Murray H. G. Munro Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 4 ÏàËÆ¶È:53.3% Tetrahedron Letters 2000 41 465-469 Studies toward the total synthesis of Sch 202596, an antagonist of the galanin receptor subtype GalR1: synthesis of geodin, the spirocoumaranone subunit of Sch 202596 Tadashi Katoh, Osamu Ohmori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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