Journal of Natural Products · 2009 · 62 citations · 15 references
Natural SciencesChemistryMedicinal ChemistryDrug DiscoveryMycologyOrganic ChemistryAromatic PlantsFungal Secondary MetabolitesHeterocyclic ChemistryStructure-activity Relationship AnalysisBioactive ConstituentsFungal Bioactive CompoundsSpirocyclic Scaffolds
A study on the chemical constituents of the endophytic fungus Preussia sp. led to the isolation of three new spirobisnaphthalene analogues, spiropreussione A (1), spiropreussione B (2), and spiropreussomerin A (3). Compound 2 is a spirobisnaphthalene analogue with a cyclopenteno-naphthoindene fragment bridged to a 1,8-dioxygenated naphthalene fragment, and compound 1 is the second compound in this series with a spiro-nonadiene skeleton. The structures of 1-3 were elucidated using spectroscopic data interpretation. Compound 1 showed cytotoxicity toward A2780 and BEL-7404 cells with IC(50) values of 2.4 and 3.0 microM, respectively, and weak activity against Staphylococcus aureus (CMCC B26003) with a MIC value of 25 microM.
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Karsten Krohn, Andreas Michel, Ülrich Flörke et al. · Liebigs Annalen der Chemie · 1994 · 110 citations
Karsten Krohn, Andreas Michel, Ülrich Flörke et al. · Liebigs Annalen der Chemie · 1994 · 98 citations
Donald T. Wicklow, Biren K. Joshi, William R. Gamble et al. · Applied and Environmental Microbiology · 1998 · 94 citations · Full text