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СÐÂa: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-10-19 00:14:06
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СÐÂa: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-10-19 00:14:06
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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£º¹²²éµ½52¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 7-epi-sclerotiorin ÏàËÆ¶È:95.4% Chemical & Pharmaceutical Bulletin 1995 43 1307-1310 Four New Chlorinated Azaphilones, Helicusins A-D, Closely Related to 7-epi-Sclerotiorin, from an Ascomycetous Fungus, Talaromyces helicus Eiji YOSHIDA,Haruhiro FUJIMOTO,Miyuki BABA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (+)-sclerotiorin ÏàËÆ¶È:95.4% The Journal of Antibiotics 1995 48 913-923 Azaphilones with Endothelin Receptor Binding Activity Produced by Penicillium sclerotiorum: Taxonomy, Fermentation, Isolation, Structure Elucidation and Biological Activity L. PAIRET, S. K. WRIGLEY, I. CHETLAND, E. E. REYNOLDS, M. A. HAYES, J. HOLLOWAY, A. M. AINSWORTH, W. KATZER, X-M. CHENG, D. J. HUPE, P. CHARLTON, A. M. DOHERTY Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound C21H23O5Cl ÏàËÆ¶È:95.4% Journal of Agricultural and Food Chemistry 2007 55 2879-2883 Sclerotiorin, a Novel Inhibitor of Lipoxygenase from Penicillium frequentans C. Chidananda and A. P. Sattur Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ºË´ÔÇàÃ¹ËØ C21H23ClO5 ÏàËÆ¶È:95.4% Journal of Chinese Medicinal Materials 2011 34 544-546 Secondary Metabolites of Seaweed Endophytic Fungi ZJ27 in the South China Sea Coast XIAO Bi-hong, SHE Zhi-gang, LEI Xiao-ling, CHEN Bin, HUANG Cai-huan, XU Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . helicusin A methyl ester C26H29ClO7 ÏàËÆ¶È:80.7% Chemical & Pharmaceutical Bulletin 1995 43 1307-1310 Four New Chlorinated Azaphilones, Helicusins A-D, Closely Related to 7-epi-Sclerotiorin, from an Ascomycetous Fungus, Talaromyces helicus Eiji YOSHIDA,Haruhiro FUJIMOTO,Miyuki BABA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . helicusin A C25H27ClO7 ÏàËÆ¶È:80% Chemical & Pharmaceutical Bulletin 1995 43 1307-1310 Four New Chlorinated Azaphilones, Helicusins A-D, Closely Related to 7-epi-Sclerotiorin, from an Ascomycetous Fungus, Talaromyces helicus Eiji YOSHIDA,Haruhiro FUJIMOTO,Miyuki BABA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . helicusin C C25H27ClO7 ÏàËÆ¶È:80% Chemical & Pharmaceutical Bulletin 1995 43 1307-1310 Four New Chlorinated Azaphilones, Helicusins A-D, Closely Related to 7-epi-Sclerotiorin, from an Ascomycetous Fungus, Talaromyces helicus Eiji YOSHIDA,Haruhiro FUJIMOTO,Miyuki BABA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . helicusin D C25H27ClO7 ÏàËÆ¶È:80% Chemical & Pharmaceutical Bulletin 1995 43 1307-1310 Four New Chlorinated Azaphilones, Helicusins A-D, Closely Related to 7-epi-Sclerotiorin, from an Ascomycetous Fungus, Talaromyces helicus Eiji YOSHIDA,Haruhiro FUJIMOTO,Miyuki BABA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . helicusin C methyl ester C26H29ClO7 ÏàËÆ¶È:76.9% Chemical & Pharmaceutical Bulletin 1995 43 1307-1310 Four New Chlorinated Azaphilones, Helicusins A-D, Closely Related to 7-epi-Sclerotiorin, from an Ascomycetous Fungus, Talaromyces helicus Eiji YOSHIDA,Haruhiro FUJIMOTO,Miyuki BABA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . helicusin B C25H27ClO7 ÏàËÆ¶È:76% Chemical & Pharmaceutical Bulletin 1995 43 1307-1310 Four New Chlorinated Azaphilones, Helicusins A-D, Closely Related to 7-epi-Sclerotiorin, from an Ascomycetous Fungus, Talaromyces helicus Eiji YOSHIDA,Haruhiro FUJIMOTO,Miyuki BABA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3-N-methylsclerotiorinamine C22H26NO4Cl ÏàËÆ¶È:68.1% Journal of Natural Products 2000 63 1303-1305 8-O-Methylsclerotiorinamine, Antagonist of the Grb2-SH2 Domain, Isolated from Penicillium multicolor Ji-Youn Nam,Hyae-Kyeong Kim,Ju-Young Kwon,Mi Young Han,Kwang-Hee Son,Un Chul Lee, Jung-Do Choi, and Byoung-Mog Kwon Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (-)-rotiorin C23H24O5 ÏàËÆ¶È:65.2% Journal of Natural Products 2006 69 891-895 Antifungal Azaphilones from the Fungus Chaetomium cupreum CC3003 Somdej Kanokmedhakul, Kwanjai Kanokmedhakul, Pitak Nasomjai, Sysavad Louangsysouphanh,Kasem Soytong, Minoru Isobe, Palangpon Kongsaeree, Samran Prabpai, and Apichart Suksamrarn Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 5-chloroisorotiorin ÏàËÆ¶È:65.2% The Journal of Antibiotics 1995 48 913-923 Azaphilones with Endothelin Receptor Binding Activity Produced by Penicillium sclerotiorum: Taxonomy, Fermentation, Isolation, Structure Elucidation and Biological Activity L. PAIRET, S. K. WRIGLEY, I. CHETLAND, E. E. REYNOLDS, M. A. HAYES, J. HOLLOWAY, A. M. AINSWORTH, W. KATZER, X-M. CHENG, D. J. HUPE, P. CHARLTON, A. M. DOHERTY Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . isochromophilone VI C25H30NO6Cl ÏàËÆ¶È:65.2% Australian Journal of Chemistry 2003 56 13-15 Isochromophilone IX, a Novel GABA-Containing Metabolite Isolated from a Cultured Fungus, Penicillium sp. Adam P. Michael, Emily J. Grace, Mike Kotiw and Russell A. Barrow Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . sclerotioramine C21H24ClNO4 ÏàËÆ¶È:63.6% Journal of Natural Products 2010 73 942-948 Chemical Epigenetics Alters the Secondary Metabolite Composition of Guttate Excreted by an Atlantic-Forest-Soil-Derived Penicillium citreonigrum Xiaoru Wang, Jos¨¦ G. Sena Filho, Ashley R. Hoover, Jarrod B. King, Trevor K. Ellis, Douglas R. Powell and Robert H. Cichewicz Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Deacetylsclerotiorin C19H21ClO4 ÏàËÆ¶È:63.6% Marine Drugs 2013 11 800-816 Helicusin E, Isochromophilone X and Isochromophilone XI: New Chloroazaphilones Produced by the Fungus Bartalinia robillardoides Strain LF550 Nils Jansen, Birgit Ohlendorf, Arlette Erhard, Torsten Bruhn, Gerhard Bringmann and Johannes F. Imhoff Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . isochromophilone VI C23H28NO5Cl ÏàËÆ¶È:60.8% The Journal of Antibiotics 1995 48 696-702 Isochromophilones III - VI, Inhibitors of Acyl-CoA: Cholesterol Acyltransferase Produced by Penicillium multicolor FO-3216 NORIKO ARAI, KAZURO SHIOMI, HIROSHI TOMODA, NORIKO TABATA, DA JUN YANG, ROKURO MASUMA, TOMOYA KAWAKUBO, SATOSHI OMURA Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 9-acetyl-5-chloro-3-(3,5-dimethyl-1,3-heptadienyl)-6a-methyl-6H-furo[2,3-h]-2-benzopyran-6,8(6aH)-di-one C23H24O5Cl ÏàËÆ¶È:60.8% The Journal of Antibiotics 1996 49 689-692 Synthesis and Inhibitory Activities of Isochromophilone Analogues against gp120-CD4 Binding XUE-LONG SUN, HIROAKI TAKAYANAGI, KEIICHI MATSUZAKI, HARUO TANAKA, KIMIO FURUHATA, SATOSHI OMURA Structure 13C NMR ̼Æ×Ä£Äâͼ |

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