Organic Letters · 2019 · 20 citations · 15 references
Life SciencesChemistryMicrobiologyBioorganic ChemistryMycologyOrganic ChemistryFungal Secondary MetabolitesMetabolite IdentificationMolecular SimilarityRetrosynthetic AnalysisChemical Shift AnalysisEnergy Dispersive X-ray SpectroscopyEnergy-dispersive X-ray SpectroscopyQuinone BiosynthesisQuinone ChemistryQuinone FormationThioether LinkersThioether Metabolites
The chemical analysis of a Streptomyces strain, from a Korean volcanic island, discovered new benz[ a]anthracene dimers linked by a thioether bond. The structures of donghaesulfins A and B (1 and 2) were elucidated by spectroscopic analysis including energy-dispersive X-ray. Their configurations were determined by ROESY NMR data, DP4 calculations, the modified Mosher's method, and ECD calculations. Donghaesulfins A (1) induced quinone reductase, whereas donghaesulfin B (2) displayed antiangiogenesis activity.
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Gerhard Bringmann, Stefan Tasler, H. Endress et al. · Journal of the American Chemical Society · 2001 · 233 citations