Communiols E-H: New polyketide metabolites from the coprophilous fungus Podospora communis

Página do item simplificado
dc.contributor.authorChe, Yongsheng
dc.contributor.authorAraujo, Angela R. [UNESP]
dc.contributor.authorGloer, James B.
dc.contributor.authorScott, James A.
dc.contributor.authorMalloch, David
dc.contributor.institutionUniversity of Iowa
dc.contributor.institutionUniversity of Toronto
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:21:17Z
dc.date.available2014-05-27T11:21:17Z
dc.date.issued2005-03-01
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.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.format.extent435-438
dc.identifierhttp://dx.doi.org/10.1021/np049592f
dc.identifier.citationJournal of Natural Products, v. 68, n. 3, p. 435-438, 2005.
dc.identifier.doi10.1021/np049592f
dc.identifier.issn0163-3864
dc.identifier.orcid0000-0001-7616-9652
dc.identifier.scopus2-s2.0-17444373466
dc.identifier.urihttp://hdl.handle.net/11449/68141
dc.language.isoeng
dc.relation.ispartofJournal of Natural Products
dc.relation.ispartofjcr3.885
dc.relation.ispartofsjr1,368
dc.rights.accessRightsAcesso restrito
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.typeArtigo
dcterms.licensehttp://pubs.acs.org/paragonplus/copyright/jpa_form_a.pdf
unesp.author.lattes0037579054083160[2]
unesp.author.orcid0000-0001-7616-9652[2]

Arquivos

Coleções

Artigos