Spirocyclic lactams and curvulinic acid derivatives from the endophytic fungus Curvularia lunata and their antibacterial and antifungal activities
| dc.contributor.author | Hilario, Felipe [UNESP] | |
| dc.contributor.author | Polinário, Giulia [UNESP] | |
| dc.contributor.author | de Amorim, Marcelo Rodrigues [UNESP] | |
| dc.contributor.author | de Sousa Batista, Victor [UNESP] | |
| dc.contributor.author | do Nascimento Júnior, Nailton Monteiro [UNESP] | |
| dc.contributor.author | Araújo, Angela Regina [UNESP] | |
| dc.contributor.author | Bauab, Taís Maria [UNESP] | |
| dc.contributor.author | dos Santos, Lourdes Campaner [UNESP] | |
| dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
| dc.date.accessioned | 2020-12-12T02:32:42Z | |
| dc.date.available | 2020-12-12T02:32:42Z | |
| dc.date.issued | 2020-03-01 | |
| dc.description.abstract | Curvularia 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.affiliation | São Paulo State University (UNESP) School of Pharmaceutical Sciences, Road Araraquara-Jaú km1 | |
| dc.description.affiliation | São Paulo State University (UNESP) Institute of Chemistry, Av. Prof. Francisco Degni n.55 | |
| dc.description.affiliationUnesp | São Paulo State University (UNESP) School of Pharmaceutical Sciences, Road Araraquara-Jaú km1 | |
| dc.description.affiliationUnesp | São Paulo State University (UNESP) Institute of Chemistry, Av. Prof. Francisco Degni n.55 | |
| dc.description.sponsorship | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
| dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
| dc.description.sponsorshipId | FAPESP: 2016/05480-6 | |
| dc.identifier | http://dx.doi.org/10.1016/j.fitote.2019.104466 | |
| dc.identifier.citation | Fitoterapia, v. 141. | |
| dc.identifier.doi | 10.1016/j.fitote.2019.104466 | |
| dc.identifier.issn | 1873-6971 | |
| dc.identifier.issn | 0367-326X | |
| dc.identifier.scopus | 2-s2.0-85077359051 | |
| dc.identifier.uri | http://hdl.handle.net/11449/201444 | |
| dc.language.iso | eng | |
| dc.relation.ispartof | Fitoterapia | |
| dc.source | Scopus | |
| dc.subject | Antibacterial activity | |
| dc.subject | Curvularia lunata | |
| dc.subject | Curvulinic acid | |
| dc.subject | Paepalanthus chiquitensis | |
| dc.subject | Spirocyclic lactams | |
| dc.title | Spirocyclic lactams and curvulinic acid derivatives from the endophytic fungus Curvularia lunata and their antibacterial and antifungal activities | en |
| dc.type | Artigo | pt |
| dspace.entity.type | Publication | |
| relation.isDepartmentOfPublication | 5004bcab-94af-4939-b980-091ae9d0a19e | |
| relation.isDepartmentOfPublication.latestForDiscovery | 5004bcab-94af-4939-b980-091ae9d0a19e | |
| relation.isOrgUnitOfPublication | bc74a1ce-4c4c-4dad-8378-83962d76c4fd | |
| relation.isOrgUnitOfPublication.latestForDiscovery | bc74a1ce-4c4c-4dad-8378-83962d76c4fd | |
| unesp.campus | Universidade Estadual Paulista (UNESP), Instituto de Química, Araraquara | pt |
| unesp.department | Ciências Biológicas - FCF | pt |
| unesp.department | Química Orgânica - IQAR | pt |

