The Journal of Antibiotics · 1995 · 60 citations · 12 references
MedicineMedicinal ChemistryPharmacologyAntimicrobial PharmacologyAntibacterial AgentsAntibacterial PharmacologyAntibiotic ProductionAntimicrobial PeptidesAntibiotic DiscoveryBiological Activity FeaturesDe Novo Structure ElucidationPeptide Structure-activity RelationshipsSubstituent Effects On Biological Activity
Aurantimycins A (1), B (2) and C (3) were isolated from the mycelium of Streptomyces aurantiacus JA 4570 as new representatives of the azinothricin group of hexadepsipeptide antibiotics. Their structures were settled by X-ray diffraction analysis of crystalline aurantimycin A (1), high field homo- and heteronuclear 2D NMR experiments, high-resolution mass spectrometry and amino acid analysis. Aurantimycins are characterized by a new side chain containing fourteen carbon atoms. They display strong activity against Gram-positive bacteria and cytotoxic effects against L-929 mouse fibroblast cells.
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