Helvetica Chimica Acta · 2011 · 43 citations · 15 references
Life SciencesBotanyMedicinal ChemistryBioorganic ChemistryMycologyPlant BiochemistryFungal BiochemistryFungal Natural Product BiosynthesisFungal Secondary MetabolitesBioactive Compounds From Marine FungiBioactive Fungal MetabolitesCytotoxicity AssaysEndophytic Fungal MetabolitesFungal Bioactive CompoundsMarine Fungal Natural ProductsPlant-associated Fungal MetabolitesStructure Elucidation Of Fungal Metabolites
Abstract Four new dimeric naphtho‐ γ ‐pyrones, named rubasperone D ( 1 ), rubasperone E ( 2 ), rubasperone F ( 3 ), and its atropisomer rubasperone G ( 4 ), together with four known monomeric naphtho‐ γ ‐pyrones, TMC 256 A1 ( 5 ), rubrofusarin B ( 6 ), fonsecin ( 7 ), and flavasperone ( 8 ), were isolated from the mangrove endophytic fungus Aspergillus tubingensis (GX1‐5E) cultivated in solid rice medium. Their structures were elucidated by spectroscopic methods, including IR, 1D‐ and 2D‐NMR, and MS. In the in vitro cytotoxicity assays, 5 displayed inhibitory activities against tumor cell lines of MCF‐7, MDA‐MB‐435, Hep3B, Huh7, SNB19, and U87 MG with IC 50 values between 19.92 and 47.98 μ M . Compounds 1, 6 , and 8 also showed mild cytotoxic activity.
15
THE CALCULATION OF THE DOSAGE‐MORTALITY CURVE
C. I. Bliss · Annals of Applied Biology · 1935 · 1.1K citations
Pharmacy, Biostatistics, Toxicology +17
John W. Blunt, Brent R. Copp, Murray H. G. Munro et al. · Natural Product Reports · 2010 · 407 citations · Full text
Song Wang, Xiao‐Ming Li, Franka Teuscher et al. · Journal of Natural Products · 2006 · 276 citations