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Spirocyclic lactams and curvulinic acid derivatives from the endophytic fungus Curvularia lunata and their antibacterial and antifungal activities

dc.contributor.authorHilario, Felipe [UNESP]
dc.contributor.authorPolinário, Giulia [UNESP]
dc.contributor.authorde Amorim, Marcelo Rodrigues [UNESP]
dc.contributor.authorde Sousa Batista, Victor [UNESP]
dc.contributor.authordo Nascimento Júnior, Nailton Monteiro [UNESP]
dc.contributor.authorAraújo, Angela Regina [UNESP]
dc.contributor.authorBauab, Taís Maria [UNESP]
dc.contributor.authordos Santos, Lourdes Campaner [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2020-12-12T02:32:42Z
dc.date.available2020-12-12T02:32:42Z
dc.date.issued2020-03-01
dc.description.abstractCurvularia lunata, isolated from the capitula of Paepalanthus chiquitensis (Eriocaulaceae), was cultured in potato dextrose broth (PDB) medium. The ethyl acetate extract yielded two new spirocyclic γ-lactams (3 and 4), and five known compounds, namely: triticones E (1) and F (2), 5-O-methylcurvulinic acid (5), curvulinic acid (6) and curvulin (7). Their structures were elucidated by spectroscopic analysis and by the comparison with literature data. Besides, a computational study was used to elucidate the absolute configuration of the C − 3′ in the compounds (3) and (4). The extract and the compounds (1 and 2), (6) and (7) were assayed against gram-positive and gram-negative bacteria and fluconazole-resistant yeast. The triticones (1) and (2) showed good antibacterial activity for Escherichia coli, with a minimum inhibitory concentration of 62.5 μg/mL.en
dc.description.affiliationSão Paulo State University (UNESP) School of Pharmaceutical Sciences, Road Araraquara-Jaú km1
dc.description.affiliationSão Paulo State University (UNESP) Institute of Chemistry, Av. Prof. Francisco Degni n.55
dc.description.affiliationUnespSão Paulo State University (UNESP) School of Pharmaceutical Sciences, Road Araraquara-Jaú km1
dc.description.affiliationUnespSão Paulo State University (UNESP) Institute of Chemistry, Av. Prof. Francisco Degni n.55
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2016/05480-6
dc.identifierhttp://dx.doi.org/10.1016/j.fitote.2019.104466
dc.identifier.citationFitoterapia, v. 141.
dc.identifier.doi10.1016/j.fitote.2019.104466
dc.identifier.issn1873-6971
dc.identifier.issn0367-326X
dc.identifier.scopus2-s2.0-85077359051
dc.identifier.urihttp://hdl.handle.net/11449/201444
dc.language.isoeng
dc.relation.ispartofFitoterapia
dc.sourceScopus
dc.subjectAntibacterial activity
dc.subjectCurvularia lunata
dc.subjectCurvulinic acid
dc.subjectPaepalanthus chiquitensis
dc.subjectSpirocyclic lactams
dc.titleSpirocyclic lactams and curvulinic acid derivatives from the endophytic fungus Curvularia lunata and their antibacterial and antifungal activitiesen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublication5004bcab-94af-4939-b980-091ae9d0a19e
relation.isDepartmentOfPublication.latestForDiscovery5004bcab-94af-4939-b980-091ae9d0a19e
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
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unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentCiências Biológicas - FCFpt
unesp.departmentQuímica Orgânica - IQARpt

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