Abstract
A novel macrocyclic dimer lactone, named verbalactone, was isolated from the roots of Verbascum undulatum and exhibited interesting antibacterial activity. It is the first time that 1,7-dioxacyclododecane is reported as the ring system of a natural product. The structure and the absolute stereochemistry of the new compound were determined by spectral methods and chemical correlation.
MeSH terms
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Anti-Bacterial Agents / chemistry
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Anti-Bacterial Agents / isolation & purification*
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Anti-Bacterial Agents / pharmacology
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Chromatography, Thin Layer
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Decanoic Acids / chemistry
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Decanoic Acids / pharmacology
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Enterobacter aerogenes / drug effects
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Escherichia coli / drug effects
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Greece
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Klebsiella pneumoniae / drug effects
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Lacticaseibacillus casei / drug effects
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Lactones / chemistry
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Lactones / isolation & purification*
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Lactones / pharmacology
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Magnetic Resonance Spectroscopy
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Mass Spectrometry
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Microbial Sensitivity Tests
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Molecular Conformation
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Molecular Structure
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Plant Roots / chemistry
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Plants, Medicinal / chemistry*
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Pseudomonas aeruginosa / drug effects
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Salmonella enteritidis / drug effects
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Spectrophotometry, Infrared
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Staphylococcus aureus / drug effects
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Staphylococcus epidermidis / drug effects
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Stereoisomerism
Substances
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3,5-dihydroxydecanoic acid
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Anti-Bacterial Agents
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Decanoic Acids
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Lactones
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verbalactone