New Bioactive Metabolites from a Freshwater Isolate of the Fungus Kirschsteiniothelia sp

The new cytotoxic naphthoquinone dimer kirschsteinin [5], two new chlorinated diphenyl ethers 8 and 9, three known naphthoquinone derivatives 1, 2, and 7, a monoacetyl derivative of 2, and the (-)-enantiomer of O-methylasparvenone [4], have been isolated from a previously undescribed species of Kirs...

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Published inJournal of natural products (Washington, D.C.) Vol. 55; no. 8; pp. 1093 - 1099
Main Authors Poch, Gregory K, Gloer, James B, Shearer, Carol A
Format Journal Article
LanguageEnglish
Published Washington, DC American Chemical Society 01.08.1992
Glendale, AZ American Society of Pharmacognosy
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Summary:The new cytotoxic naphthoquinone dimer kirschsteinin [5], two new chlorinated diphenyl ethers 8 and 9, three known naphthoquinone derivatives 1, 2, and 7, a monoacetyl derivative of 2, and the (-)-enantiomer of O-methylasparvenone [4], have been isolated from a previously undescribed species of Kirschsteiniothelia. The structures of these compounds were assigned primarily by nmr studies and by spectral comparisons.
Bibliography:istex:D14D2CCA939E62A3AAEA5DA49749BE4C22F44315
ark:/67375/TPS-2Q79J06P-8
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0163-3864
1520-6025
DOI:10.1021/np50086a010