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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/68141
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dc.contributor.authorChe, Yongsheng-
dc.contributor.authorAraujo, Angela R.-
dc.contributor.authorGloer, James B.-
dc.contributor.authorScott, James A.-
dc.contributor.authorMalloch, David-
dc.date.accessioned2014-05-27T11:21:17Z-
dc.date.accessioned2016-10-25T18:20:30Z-
dc.date.available2014-05-27T11:21:17Z-
dc.date.available2016-10-25T18:20:30Z-
dc.date.issued2005-03-01-
dc.identifierhttp://dx.doi.org/10.1021/np049592f-
dc.identifier.citationJournal of Natural Products, v. 68, n. 3, p. 435-438, 2005.-
dc.identifier.issn0163-3864-
dc.identifier.urihttp://hdl.handle.net/11449/68141-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/68141-
dc.description.abstractCommuniols 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.en
dc.format.extent435-438-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectcyclopentane derivative-
dc.subjectfuran derivative-
dc.subjectlactone-
dc.subjectantifungal agent-
dc.subjectantiinfective agent-
dc.subjectcommuniol A-
dc.subjectcommuniol B-
dc.subjectcommuniol C-
dc.subjectcommuniol D-
dc.subjectcommuniol E-
dc.subjectcommuniol F-
dc.subjectcommuniol G-
dc.subjectcommuniol H-
dc.subjectcyclopentene derivative-
dc.subjectfuranocyclopentane derivative-
dc.subjectfuranocyclopentene derivative-
dc.subjectgamma lactone derivative-
dc.subjectnatural product-
dc.subjectpolyketide-
dc.subjectunclassified drug-
dc.subjectchemical structure-
dc.subjectchemistry-
dc.subjectEcuador-
dc.subjectisolation and purification-
dc.subjectmass spectrometry-
dc.subjectnuclear magnetic resonance-
dc.subjectPodospora-
dc.subjectUnited States-
dc.subjectantibacterial activity-
dc.subjectantifungal activity-
dc.subjectBacillus subtilis-
dc.subjectCandida albicans-
dc.subjectcarbon nuclear magnetic resonance-
dc.subjectdrug isolation-
dc.subjectdrug structure-
dc.subjectfungus culture-
dc.subjectfungus isolation-
dc.subjectnonhuman-
dc.subjectnuclear magnetic resonance spectroscopy-
dc.subjectnuclear Overhauser effect-
dc.subjectPodospora communis-
dc.subjectproton nuclear magnetic resonance-
dc.subjectStaphylococcus aureus-
dc.subjectstereochemistry-
dc.subjectstructure analysis-
dc.subjectCalifornia-
dc.subjectCyclopentanes-
dc.subjectFurans-
dc.subjectLactones-
dc.subjectMass Spectrometry-
dc.subjectMolecular Structure-
dc.subjectNuclear Magnetic Resonance, Biomolecular-
dc.subjectCoprophilous-
dc.subjectFungi-
dc.titleCommuniols E-H: New polyketide metabolites from the coprophilous fungus Podospora communisen
dc.typeoutro-
dc.contributor.institutionUniversity of Iowa-
dc.contributor.institutionUniversity of Toronto-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Chemistry University of Iowa, Iowa City, IA 52242-
dc.description.affiliationDepartment of Botany University of Toronto, Toronto, Ont. M5S 1A1-
dc.description.affiliationInstituto de Quimica UNESP, Rua Francisco Degni, s/n, 14800-900 Araraquara, SP-
dc.description.affiliationUnespInstituto de Quimica UNESP, Rua Francisco Degni, s/n, 14800-900 Araraquara, SP-
dc.identifier.doi10.1021/np049592f-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Natural Products-
dc.identifier.scopus2-s2.0-17444373466-
dc.identifier.orcid0000-0001-7616-9652pt
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