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 in | Journal of natural products (Washington, D.C.) Vol. 55; no. 8; pp. 1093 - 1099 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
American Chemical Society
01.08.1992
Glendale, AZ American Society of Pharmacognosy |
Subjects | |
Online Access | Get full text |
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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. |
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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 |