Magnetic Resonance in Chemistry · 2011 · 38 citations · 19 references
Life SciencesBiochemistryMicrobiologyMycologyNatural Product BiosynthesisSteroid BiochemistryFungal BiochemistryFungal DiversityFungal Natural Product BiosynthesisFungal Secondary MetabolitesMarine Natural Product BiosynthesisRed AlgaeAnomeric StereochemistryBioactive Compounds From Marine FungiFungal Bioactive CompoundsMarine Fungal EndophytesMarine Fungal MetabolitesMarine Fungal Natural ProductsMarine Fungal Secondary MetabolitesSpectroscopic Characterization
A new oxylipin, (8E,12Z)-10,11-dihydroxyoctadeca-8,12-dienoic acid (1), a new steroid, 3β,4α-dihydroxy-26-methoxyergosta-7,24(28)-dien-6-one (2), and four known steroids, episterol (3), (22E,24R)-ergosta-7,22-dien-3β,5α,6α-triol (4), (22E,24R)-ergosta-5,22-dien-3β-ol (5), and (22E,24R)-ergosta-4,6,8(14),22-tetraen-3-one (6), were isolated from the cultures of Aspergillus flavus, an endophytic fungus isolated from the marine red alga Corallina officinalis. Their structures and relative stereochemistry were elucidated by 1D, 2D NMR and mass spectroscopic techniques. 1 and 2 exhibited low activity to inhibit acetylcholinesterase and no activity against plant pathogenic fungi Colletotrichum lagenarium and Fusarium oxysporum.
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Biologically active secondary metabolites of endophytic Pezicula species
Barbara Schulz, J. Sucker, H.-J. Aust et al. · Mycological Research · 1995 · 302 citations
Life Sciences, Biochemistry, Botany +14
Aspergillus Flavus and Turkey X Disease: Toxic Metabolites of Aspergillus flavus
Brenda F. Nesbitt, J. C. O'Kelly, K. Sargeant et al. · Nature · 1962 · 247 citations