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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´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£º¹²²éµ½104¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 1,2-seco-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 . monomethylsulochrin ÏàËÆ¶È:100% 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:72.2% 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 4 . Sulochrin C17H16O7 ÏàËÆ¶È:72.2% 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 5 . sulochrin C17H16O7 ÏàËÆ¶È:72.2% 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 6 . sulochrin ÏàËÆ¶È:72.2% 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 7 . methyl 2-(2-formyl-3-hydroxy-5-methylphenoxy)-5-hydroxy-3-methoxybenzoate C17H16O7 ÏàËÆ¶È:72.2% 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 8 . Hydroxysulochrin C17H16O8 ÏàËÆ¶È:66.6% 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 9 . 2-(2,6-dihydroxy-4-methoxybenzoyl)-3,5-dimethoxybenzoic acid ÏàËÆ¶È:66.6% 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 10 . dinklagin C C20H18O6 ÏàËÆ¶È:55.5% Phytochemistry 2002 61 99-104 Dinklagins A, B and C: three prenylated flavonoids and other constituents from the twigs of Dorstenia dinklagei Bonaventure T. Ngadjui, Etienne Dongo, Berhanu M. Abegaz,Serge Fotso, Helene Tamboue Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 3 C18H16O7 ÏàËÆ¶È:55.5% Records of Natural Products 2012 6:1 28-34 Secondary Metabolites of Aspergillus sp. CM9a, an Endophytic Fungus of Cephalotaxus mannii Heng Xue, Chunhua Lu, Lanying Liang and Yuemao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Compound 3 C18H16O7 ÏàËÆ¶È:55.5% Records of Natural Products 2012 6 28-34 Secondary Metabolites of Aspergillus sp. CM9a,an Endophytic Fungus of Cephalotaxus mannii Heng Xue,Chunhua Lu,Lanying Liang and Yuemao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . mucodianin B C16H14O5 ÏàËÆ¶È:55.5% Chemical & Pharmaceutical Bulletin 2010 58 254-256 A Novel 3-Arylcoumarin and Three New 2-Arylbenzofurans from Mucuna birdwoodiana Ting Gong, Dong-Xiao Wang, Yan Yang, Ping Liu, Ruo-Yun Chen and De-Quan Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 4 ÏàËÆ¶È:55.5% 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 15 . compound 8d/1 C19H18ClN5O2 ÏàËÆ¶È:55.5% Journal of Heterocyclic Chemistry 2004 41 915-929 Unexpected formation of 1,2-dihydro-2-azolyl-and azinylisoquinolines by the reduction of the corresponding isoquinolinium salts with sodium borohydride in methanol Ibolya Prauda,M¨¢ria T¨®th-Lauritz and J¨®zsef Reiter Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 8d/3 C20H21N5O3 ÏàËÆ¶È:55.5% Journal of Heterocyclic Chemistry 2004 41 915-929 Unexpected formation of 1,2-dihydro-2-azolyl-and azinylisoquinolines by the reduction of the corresponding isoquinolinium salts with sodium borohydride in methanol Ibolya Prauda,M¨¢ria T¨®th-Lauritz and J¨®zsef Reiter Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 1,7,9-trimethoxy-3-methyl-6H-dibenzo[b,d]pyran-6-one C17H16O5 ÏàËÆ¶È:55.5% 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 |

2Â¥2013-07-23 15:23:17
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Á÷ÐÇÀáÀá: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, xiexie 2013-07-23 18:28:52
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ѯ½á¹û£º¹²²éµ½7¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 1,2-seco-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 . monomethylsulochrin ÏàËÆ¶È:100% 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:72.2% 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 4 . Sulochrin C17H16O7 ÏàËÆ¶È:72.2% 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 5 . sulochrin C17H16O7 ÏàËÆ¶È:72.2% 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 6 . sulochrin ÏàËÆ¶È:72.2% 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 7 . methyl 2-(2-formyl-3-hydroxy-5-methylphenoxy)-5-hydroxy-3-methoxybenzoate C17H16O7 ÏàËÆ¶È:72.2% |

3Â¥2013-07-23 15:24:18














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