Che, YongshengAraujo, Angela R. [UNESP]Gloer, James B.Scott, James A.Malloch, David2014-05-272014-05-272005-03-01Journal of Natural Products, v. 68, n. 3, p. 435-438, 2005.0163-3864http://hdl.handle.net/11449/68141Communiols E-H (1-4), four new polyketide-derived natural products containing furanocyclopentane, furanocyclopentene, cyclopentene, or γ-lactone moieties, have been isolated from two geographically distinct isolates of the coprophilous fungus Podospora communis. The structures of these compounds were determined by analysis of NMR and MS data. © 2005 American Chemical Society and American Society of Pharmacognosy.435-438engcyclopentane derivativefuran derivativelactoneantifungal agentantiinfective agentcommuniol Acommuniol Bcommuniol Ccommuniol Dcommuniol Ecommuniol Fcommuniol Gcommuniol Hcyclopentene derivativefuranocyclopentane derivativefuranocyclopentene derivativegamma lactone derivativenatural productpolyketideunclassified drugchemical structurechemistryEcuadorisolation and purificationmass spectrometrynuclear magnetic resonancePodosporaUnited Statesantibacterial activityantifungal activityBacillus subtilisCandida albicanscarbon nuclear magnetic resonancedrug isolationdrug structurefungus culturefungus isolationnonhumannuclear magnetic resonance spectroscopynuclear Overhauser effectPodospora communisproton nuclear magnetic resonanceStaphylococcus aureusstereochemistrystructure analysisCaliforniaCyclopentanesFuransLactonesMass SpectrometryMolecular StructureNuclear Magnetic Resonance, BiomolecularCoprophilousFungiArtigo10.1021/np049592fAcesso restrito2-s2.0-174443734660000-0001-7616-9652