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Biologically Active Metabolites from Fungi, 5. Palmarumycins C<sub>1</sub>–C<sub>16</sub> from <i>Coniothyrium</i> sp.: Isolation, Structure Elucidation, and Biological Activity
109
Citations
12
References
1994
Year
Active MetabolitesSecondary MetaboliteAntimicrobial ChemotherapyPalmarumycin C 3BiosynthesisStructure ElucidationPalmarumycins C 1Antimicrobial ResistanceBiological ActivityAntimicrobial Drug DiscoveryBiochemistryFungal PhysiologyAntimicrobial CompoundPharmacologyPalmarumycin C 2MycologyAntifungal AgentAntibioticsNatural SciencesMicrobiologyAntimicrobial PharmacodynamicsMedicine
Abstract Twelve new spiro acetal metabolites, the palmarumycins C 1 –C 8 , ( 1–8 ), C 11 ( 11 ), C 12 ( 12 ), C 15 ( 15 ), C 16 ( 16 ), and three known representatives ( 10, 13, 14 ) of this new class of antibiotics were isolated from Coniothyrium sp. The compounds show antibacterial, antifungal and herbicidal activity at concentrations of 10 −6 –10 −4 mol/l. The structures of palmarumycin C 2 ( 2 ), palmarumycin C 3 ( 3 ), and palmarumycin C 5 ( 5 ) were confirmed by X‐ray structure analysis.
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