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1 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½18¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . trypacidin ÏàËÆ¶È:100% 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 ̼Æ×Ä£Äâͼ 2 . bis-dechlorogeodin C17H14O7 ÏàËÆ¶È:61.1% The Journal of Antibiotics 1996 49 1056-1059 Dechlorogeodin and Its New Dihydro Derivatives, Fungal Metabolites with Herbicidal Activity YOSHITAKE TANAKA, KEIICHI MATSUZAKI, CHONG-LIN ZHONG, HIROSHI YOSHIDA, TOMOYA KAWAKUBO, ROKURO MASUMA, HARUO TANAKA, SATOSHI OMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 12 C19H18O8 ÏàËÆ¶È:52.6% Tetrahedron 2012 68 4107-4111 Chemical synthesis of funicone analogs Emiliano Manzo, Maria Letizia Ciavatta Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . geodin C17H12Cl2O7 ÏàËÆ¶È:50% 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 ̼Æ×Ä£Äâͼ 5 . quinquangulin C16H14O5 ÏàËÆ¶È:50% Journal of Natural Products 2001 64 1153-1156 A New Naphthopyrone Derivative from Cassia quinquangulata and Structural Revision of Quinquangulin and Its Glycosides Xing-Cong Li, D. Chuck Dunbar, Hala N. ElSohly, Melissa R. Jacob, Alison C. Nimrod,Larry A. Walker, and Alice M. Clark Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . nidulalin A C16H14O6 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1994 42 1720-1723 Structures of a New Dihydroxanthone Derivative, Nidulalin A, and a New Benzophenone Derivative, Nidulalin B, from Emericella nidulans Nobuo KAWAHARA,Setsuko SEKITA,Motoyoshi SATAKE,Shun-ichi UDAGAWA and Ken-ichi KAWAI Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . nidulalin A ÏàËÆ¶È:50% 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 ̼Æ×Ä£Äâͼ 8 . 1-hydroxy-3,6,7-trimethoxyxanthone acetate C18H16O7 ÏàËÆ¶È:50% Phytochemistry 1991 30 2061-2065 Two xanthones from Polygala tenuifolia Yukinobu Ikeya, Kô Sugama, Minoru Okada, Hiroshi Mitsuhashi Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . gonytolide C C16H16O7 ÏàËÆ¶È:50% Organic Letters 2011 Vol. 13, No. 17 4624-4627 Structures of the Dimeric and Monomeric Chromanones, Gonytolides A C, Isolated from the Fungus Gonytrichum sp. And Their Promoting Activities of Innate Immune Responses Haruhisa Kikuchi, Masato Isobe, Mizuki Sekiya, Yuko Abe, Tsuyoshi Hoshikawa,Kazunori Ueda, Shoichiro Kurata, Yasuhiro Katou, and Yoshiteru Oshima Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (¡À)-geodin ÏàËÆ¶È:50% 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 ̼Æ×Ä£Äâͼ 11 . 1,7,9-trimethoxy-3-methyl-6H-dibenzo[b,d]pyran-6-one C17H16O5 ÏàËÆ¶È:50% Heterocycles 2007 74 265-271 Synthesis of Alternariol through an Intramolecular Biaryl Coupling Reaction Using Palladium Reagent Hitoshi Abe, Tomoko Fukumoto, Yasuo Takeuchi, and Takashi Harayama Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Compound 21 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry Letters 2000 10 1755-1757 Diels¨Calder approach to tetralin-based constrained ¦Á-amino acid derivatives Sambasivarao Kotha, Thota Ganesh, Arun Kumar Ghosh Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 2-(3'-chloro-4'-hydroxy-2'-methoxy-6'-methoxycarbonylphenoxy)-6-hydroxy-4-methylbenzoic acid C17H15O8Cl ÏàËÆ¶È:50% Journal of the Chemical Society, Perkin Transactions 1 1996 1419-1425 Metabolites of the higher fungi. Part 29. Maldoxin, maldoxone, dihydromaldoxin, isodihydromaldoxin and dechlorodihydromaldoxin. A spirocyclohexadienone, a depsidone and three diphenyl ethers: keys in the depsidone biosynthetic pathway from a member of the Monilola O. Adeboya, Raymond L. Edwards, Thomas Lassøe, Derek J. Maitland, Len Shields and Anthony J. S. Whalley Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . dechlorodihydromaldoxin C17H16O8 ÏàËÆ¶È:50% Journal of the Chemical Society, Perkin Transactions 1 1996 1419-1425 Metabolites of the higher fungi. Part 29. Maldoxin, maldoxone, dihydromaldoxin, isodihydromaldoxin and dechlorodihydromaldoxin. A spirocyclohexadienone, a depsidone and three diphenyl ethers: keys in the depsidone biosynthetic pathway from a member of the Monilola O. Adeboya, Raymond L. Edwards, Thomas Lassøe, Derek J. Maitland, Len Shields and Anthony J. S. Whalley Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (+)-geodin ÏàËÆ¶È:50% The Journal of Antibiotics 2005 58 583-589 Identification and Preliminary SAR Studies of (+)-Geodin as a Glucose Uptake Stimulator for Rat Adipocytes FREE Seiichi Sato, Noriyuki Okusa, Akiyo Ogawa, Takao Ikenoue, Tetsuya Seki and Takashi Tsuji Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 5,3',4'-trihydroxy-6,7,5'-trimethoxyflavone ÏàËÆ¶È:50% Biological and Pharmaceutical Bulletin 2002 25 875-879 Antiproliferative Constituents in Plants 10. Flavones from the Leaves of Lantana montevidensis BRIQ. and Consideration of Structure¨CActivity Relationship Tsuneatsu Nagao, Fumiko Abe, Junei Kinjo, Hikaru Okabe Structure 13C NMR ̼Æ×Ä£Äâͼ |

4Â¥2013-07-26 15:51:53
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°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½43¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 1,2-seco-trypacidin ÏàËÆ¶È:90% 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 ̼Æ×Ä£Äâͼ 2 . monomethylsulochrin ÏàËÆ¶È:75% 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 ̼Æ×Ä£Äâͼ 3 . Sulochrin C17H16O7 ÏàËÆ¶È:65% 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 ̼Æ×Ä£Äâͼ 4 . sulochrin C17H16O7 ÏàËÆ¶È:65% 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 ̼Æ×Ä£Äâͼ 5 . methyl 2-(2-formyl-3-hydroxy-5-methylphenoxy)-5-hydroxy-3-methoxybenzoate C17H16O7 ÏàËÆ¶È:65% 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 ̼Æ×Ä£Äâͼ 6 . Hydroxysulochrin C17H16O8 ÏàËÆ¶È:60% 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 ̼Æ×Ä£Äâͼ 7 . sulochrin ÏàËÆ¶È:60% 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 ̼Æ×Ä£Äâͼ 8 . sulochrin C17H16O7 ÏàËÆ¶È:55% 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 ̼Æ×Ä£Äâͼ 9 . compound 3c ÏàËÆ¶È:55% Journal of Natural Products 1979 Vol 42 264-270 Two New C-Benzylated Flavanones From Uvaria chamae and 13C NMR Analysis of Flavanone Methyl Ethers Hala N. El-Sohly, William L. Lasswell Jr., Charles D. Hufford Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 4 ÏàËÆ¶È:55% 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 ̼Æ×Ä£Äâͼ 11 . 1-benzyloxy-7,9-dimethoxy-3-methyl-6H-dibenzo[b,d]pyran-6-one C23H20O5 ÏàËÆ¶È:55% Heterocycles 2007 74 265-271 Synthesis of Alternariol through an Intramolecular Biaryl Coupling Reaction Using Palladium Reagent Hitoshi Abe, Tomoko Fukumoto, Yasuo Takeuchi, and Takashi Harayama Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Sulochrin C17H16O7 ÏàËÆ¶È:55% 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 ̼Æ×Ä£Äâͼ 13 . 6-hydroxyl-deoxyfunicone C19H18O8 ÏàËÆ¶È:55% Phytochemistry Letters 2013 6 14-17 Metabolites from Penicillium sp., an endophytic fungus from the liverwort Riccardia multifida (L.) S. Gray Yang Jiao, Xin Zhang, Lei Wang, Gang Li, Jin-Chuan Zhou, Hong-Xiang Lou Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . methyl asterrate ÏàËÆ¶È:55% Chinese Journal of Natural Medicines 2012 10 36-39 Chemical constituents of Allophylus longipes Xiang-Yun ZHANG, Xiang-Hai CAI, Xiao-Dong LUO Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 2-(2,6-dihydroxy-4-methoxybenzoyl)-3,5-dimethoxybenzoic acid ÏàËÆ¶È:55% 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 ̼Æ×Ä£Äâͼ 16 . 1-(2-Hydroxy-6-methoxyphenyl)-1,3-butanedione C11H12O4 ÏàËÆ¶È:54.5% Tetrahedron 2012 68 6948-6956 Access to 2-alkyl chromanones via a conjugate addition approach Louise A. Stubbing, Freda F. Li, Daniel P. Furkert, Vittorio E. Caprio, Margaret A. Brimble Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Compound 5 C21H19NO6 ÏàËÆ¶È:52.3% Bioorganic & Medicinal Chemistry Letters 2005 15 2795-2798 Dihydroindenoisoquinolines function as prodrugs of indenoisoquinolines Xiangshu Xiao, Ze-Hong Miao, Smitha Antony, Yves Pommier, Mark Cushman Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . N-((R)-2-(5-chloro-2-(4-methoxypyridin-2-yl)-6-methylpyrimidin-4-ylamino)-1-phenylethyl)-4-(piperazin-1-yl)butanamide C27H34ClN7O2 ÏàËÆ¶È:52.1% Bioorganic & Medicinal Chemistry 2013 21 2600-2617 Pyridinylpyrimidines selectively inhibit human methionine aminopeptidase-1 Pengtao Zhang, Xinye Yang, Feiran Zhang, Sandra B. Gabelli, Renxiao Wang, Yihua Zhang, Shridhar Bhat, Xiaochun Chen, Manuel Furlani, L. Mario Amzel, Jun O. Liu, Dawei Ma Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . disparacetylfuran A C24H20O6 ÏàËÆ¶È:50% Journal of Natural Products 2001 64 563-568 Novel Cytotoxic 4-Phenylfuranocoumarins from Calophyllum dispar David Guilet,Jean-Jacques H¨¦lesbeux, Denis S¨¦raphin,Thierry S¨¦venet, Pascal Richomme, and Jean Bruneton Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 2-methoxygliricidol C18H16O7 ÏàËÆ¶È:50% Journal of Natural Products 1999 62 188-190 New 12a-Hydroxyrotenoids from Gliricidia sepium Bark Luca Rastrelli, Ingeborg Berger, Wolfang Kubelka, Armando Caceres, Nunziatina De Tommasi, and Francesco De Simone Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . cercophorin C C20H16O10 ÏàËÆ¶È:50% Journal of Natural Products 1996 59 765-769 Cercophorins A-C: Novel Antifungal and Cytotoxic Metabolites from the Coprophilous Fungus Cercophora areolata Authrine C. Whyte and James B. Gloer Structure 13C NMR ̼Æ×Ä£Äâͼ |

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