Abstract
Novel antifungal antibiotics, UK-2A, B and a mixture of C and D, were obtained from the mycelial cake of Streptomyces sp. 517-02. All of the UK-2 compounds were similar in structure to antimycin A. The antifungal activities of UK-2 compounds were as strong as that of antimycin A. However, the UK-2 compounds demonstrated weak cytotoxicity compared to antimycin A.
MeSH terms
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Animals
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Antibiotics, Antineoplastic / pharmacology
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Antifungal Agents / biosynthesis
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Antifungal Agents / isolation & purification*
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Antifungal Agents / pharmacology*
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Cell Division / drug effects
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Fermentation
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Glycine / analogs & derivatives*
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Glycine / biosynthesis
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Glycine / isolation & purification
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Glycine / pharmacology
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Humans
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Lactones / chemical synthesis
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Lactones / isolation & purification
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Lactones / pharmacology
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Mice
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Microbial Sensitivity Tests
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Oxygen Consumption / drug effects
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Pyridines / chemical synthesis
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Pyridines / isolation & purification
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Pyridines / pharmacology
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Saccharomyces cerevisiae / drug effects
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Streptomyces / metabolism*
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Tumor Cells, Cultured / drug effects
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Uridine / analogs & derivatives*
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Uridine / biosynthesis
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Uridine / isolation & purification
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Uridine / pharmacology
Substances
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Antibiotics, Antineoplastic
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Antifungal Agents
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Lactones
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Pyridines
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UK 2A
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UK 2B
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UK 2C
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UK 2D
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UK 21
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Glycine
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Uridine