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1 .     scytalol B
C16H20O6     ÏàËÆ¶È:81.2%
The Journal of Antibiotics          1998          51          387-393
Scytalols A, B, C, and D and Other Modulators of Melanin Biosynthesis from Scytalidium sp. 36-93
ECKHARD THINES, HEIDRUN ANKE, OLOV STERNER
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     scytalol D
C14H16O5     ÏàËÆ¶È:78.5%
The Journal of Antibiotics          1998          51          387-393
Scytalols A, B, C, and D and Other Modulators of Melanin Biosynthesis from Scytalidium sp. 36-93
ECKHARD THINES, HEIDRUN ANKE, OLOV STERNER
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     3,4-Dihydro-3-(4(¦Î)-hydroxy-2-oxo-pentyl)-3(¦Î),6,8-trihydroxy-1(2H)-naphthalenone
C15H18O6     ÏàËÆ¶È:73.3%
Phytochemistry Letters          2009          2          207-210
Dihydronaphthalenones from the endophytic fungus Botryosphaeria sp. BCC 8200
Masahiko Isaka, Arunrat Yangchum, Pranee Rachtawee, Punsa Khoyaiklang, Nattawut Boonyuen, Saisamorn Lumyong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     scytalol A
C15H18O6     ÏàËÆ¶È:73.3%
The Journal of Antibiotics          1998          51          387-393
Scytalols A, B, C, and D and Other Modulators of Melanin Biosynthesis from Scytalidium sp. 36-93
ECKHARD THINES, HEIDRUN ANKE, OLOV STERNER
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     balticol B
C12H14O5     ÏàËÆ¶È:71.4%
Chemistry & Biodiversity          2009          6          127-137
Balticols A¨CF, New Naphthalenone Derivatives with Antiviral Activity, from an Ascomycetous Fungus
Muftah A. M. Shushni, Renate Mentel, Ulrike Lindequist, and Rolf Jansen
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     balticol E
C14H18O6     ÏàËÆ¶È:71.4%
Chemistry & Biodiversity          2009          6          127-137
Balticols A¨CF, New Naphthalenone Derivatives with Antiviral Activity, from an Ascomycetous Fungus
Muftah A. M. Shushni, Renate Mentel, Ulrike Lindequist, and Rolf Jansen
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     3,4-Dihydro-3-(2(¦Î)-hydroxypropyl)-3(¦Î),6,8-trihydroxy-1(2H)-naphthalenone
C13H16O5     ÏàËÆ¶È:71.4%
Phytochemistry Letters          2009          2          207-210
Dihydronaphthalenones from the endophytic fungus Botryosphaeria sp. BCC 8200
Masahiko Isaka, Arunrat Yangchum, Pranee Rachtawee, Punsa Khoyaiklang, Nattawut Boonyuen, Saisamorn Lumyong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     (3S,4S)-3,4,8-trihydroxy-6-methoxy-3,4-dihydro-1(2H)-naphthalenone
C11H12O5     ÏàËÆ¶È:64.2%
Planta Medica          2008          74          281-286
Antimycobacterial Substances from Phaeosphaeria sp BCC8292
Pattama Pittayakhajonwut, Pairoh Sohsomboon, Aibrohim Dramae, Rapheephat Suvannakad, Sanisa Lapanun, Morakot Tantichareon
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     3,4-Dihydro-3-(2(¦Î)-hydroxypropyl)-3(¦Î),6,8-trihydroxy-1(2H)-naphthalenone
C13H16O5     ÏàËÆ¶È:64.2%
Phytochemistry Letters          2009          2          207-210
Dihydronaphthalenones from the endophytic fungus Botryosphaeria sp. BCC 8200
Masahiko Isaka, Arunrat Yangchum, Pranee Rachtawee, Punsa Khoyaiklang, Nattawut Boonyuen, Saisamorn Lumyong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     phanerosporic acid 4-methyl ether methyl ester
C24H40O5     ÏàËÆ¶È:64.2%
Phytochemistry          1989          28          2803-2806
Phanerosporic acid,a ¦Â-resorcylate obtained from Phanerochaete chrysosporium
Alberto Arnone,Gemma Assante,Gianluca Nasini,Orso Vajna De Pava
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     1-dehydroxyarthrinone
C13H20O6     ÏàËÆ¶È:64.2%
Canadian Journal of Chemistry          1997          75          768-772
New antifungal metabolites from the coprophilous fungus Cercophorasordarioides
Authrine C. Whyte, Katherine B. Gloer, James B. Gloer, Brenda Koster, David Malloch
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     3a,9a-deoxy-3a-hydroxy-1-dehydroxyarthrinone
C13H14O6     ÏàËÆ¶È:64.2%
Canadian Journal of Chemistry          1997          75          768-772
New antifungal metabolites from the coprophilous fungus Cercophorasordarioides
Authrine C. Whyte, Katherine B. Gloer, James B. Gloer, Brenda Koster, David Malloch
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     Altersolanol L
C16H20O7     ÏàËÆ¶È:62.5%
Journal of Natural Products          2009          72          626-631
Bioactive Metabolites from the Endophytic Fungus Stemphylium globuliferum Isolated from Mentha pulegium
Abdessamad Debbab,Amal H. Aly, RuAngelie Edrada-Ebel, Victor Wray, Werner E. G. M¨¹ller,Frank Totzke,Ute Zirrgiebel,Christoph Schächtele, Michael H. G. Kubbutat,Wen Han Lin,Mahjouba Mosaddak, Abdelhak Hakiki, Peter Proksch, and Rainer Ebel
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     Tetrahydroaltersolanol C
C16H20O6     ÏàËÆ¶È:62.5%
Journal of Natural Products          2012          75          189−197
Bioactive Hydroanthraquinones and Anthraquinone Dimers from a Soft Coral-Derived Alternaria sp. Fungus
Cai-Juan Zheng,Chang-Lun Shao,Zhi-Yong Guo,Jian-Feng Chen,Dong-Sheng Deng,Kai-Lin Yang,Yi-Yan Chen,Xiu-Mei Fu,Zhi-Gang She,Yong-Cheng Lin,and Chang-Yun Wang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     notholaenic acid
    ÏàËÆ¶È:60%
Journal of Natural Products          1985          Vol 48          293-298
Total Synthesis of Notholaenic Acid
Farouk S. El-Feraly, Steve F. Cheatham, James D. McChesney
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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