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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
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