Marine Drugs · 2018 · 29 citations · 11 references
Life SciencesBiochemistryMicrobiologyDrug DiscoveryMycologySteroid BiochemistryFungal BiochemistryFungal Natural Product BiosynthesisFungal Secondary MetabolitesMarine Bioactive CompoundsMarine Natural Product BiosynthesisMetabolite IdentificationBioactive Compounds From Marine FungiBioactive Fungal MetabolitesEndophytic Fungal MetabolitesFungal Bioactive CompoundsMarine Fungal MetabolitesMarine Fungal Natural ProductsMarine Fungal Secondary MetabolitesSecondary Metabolites
Chemical investigation of the marine algal-derived endophytic fungus Aspergillus alabamensis EN-547 resulted in the isolation of 4-epi-seco-shornephine A methyl ester (1) and 4-epi-seco-shornephine A carboxylic acid (2), two new secondary metabolites having a rare diketomorpholine motif, and 28-acetoxy-12β,15α,25-trihydroxyergosta-4,6,8(14),22-tetraen-3-one (3), a new highly conjugated ergostane-type steroid, together with four known metabolites (4–7). Their chemical structures were elucidated by detailed analysis of their NMR spectra, ECDs, HRESIMS, optical rotation, and X-ray crystallographic data, and by comparison with literature data as well. The antimicrobial activities of compounds 1–7 were evaluated.
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Christopher G. Pierce, Priya Uppuluri, Floyd L. Wormley et al. · Nature Protocols · 2008 · 823 citations
Christopher G. Pierce, Priya Uppuluri, Floyd L. Wormley et al. · Nature Protocols · 2008 · 775 citations · Full text
Song Wang, Xiao‐Ming Li, Franka Teuscher et al. · Journal of Natural Products · 2006 · 276 citations
Haruhiro Fujimoto, Etsuko Nakamura, Emi Okuyama et al. · Chemical and Pharmaceutical Bulletin · 2004 · 99 citations · Full text