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Integrative dereplication and molecular networking reveal potential antimicrobial agents in Kielmeyera coriacea Mart.

dc.contributor.authorCoqueiro, Aline
dc.contributor.authorWakui, Vinicius Galvão
dc.contributor.authorPilon, Alan C. [UNESP]
dc.contributor.authorCastilho, Nathália S.
dc.contributor.authorCosta, Eliângela C. C.
dc.contributor.authorMonteiro, Afif F. [UNESP]
dc.contributor.authorAnjos, Charlene S. dos
dc.contributor.authorLeandro, Luis Fernando
dc.contributor.authorMartins, Carlos Henrique Gomes
dc.contributor.authorPasqualotto Severino, Vanessa G.
dc.contributor.institutionUniversidade Tecnológica Federal do Paraná (UTFPR)
dc.contributor.institutionUniversidade Federal de Goiás (UFG)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniversidade Federal de Uberlândia (UFU)
dc.date.accessioned2025-04-29T20:12:25Z
dc.date.issued2025-01-01
dc.description.abstractKielmeyera coriacea Mart., native to Brazilian Cerrado, is traditionally used in folk medicine. The MIC against bacteria and yeasts was determined for the ethanolic extracts of roots, outer bark, leaves, and fruits. A dereplication strategy via HPLC-ESI-HRMS/MS and GNPS was used to identify known compounds and highlight potential compounds responsible for the activities. The root extract exhibited the most promising activity against a range of bacteria and fungi. This extract was selected for further fractionation, yielding n-hexane, ethyl acetate, and hydroalcoholic fractions. These were evaluated against the same microbial strains. Subsequent chromatographic analysis and bioactivity tests identified two highly active subfractions from the n-hexane and hydroalcoholic fractions. Detailed analysis using standards and databases (GNPS and Scifinder) led to the annotation of three xanthones (kielcorin, and its hydroxy- and methoxy- derivatives), three glycosylated flavonoids, and two acylphoroglucinol derivatives (garcinielliptone D e A).en
dc.description.affiliationChemistry Department Universidade Tecnológica Federal do Paraná (UTFPR), PR
dc.description.affiliationChemistry Institute Universidade Federal de Goiás, GO
dc.description.affiliationChemistry Department Universidade Estadual Paulista, SP
dc.description.affiliationInstitute of Chemistry Universidade Estadual de Campinas, SP
dc.description.affiliationInstitute of Biomedical Sciences Universidade Federal de Uberlândia
dc.description.affiliationUnespChemistry Department Universidade Estadual Paulista, SP
dc.identifierhttp://dx.doi.org/10.1080/14786419.2025.2465605
dc.identifier.citationNatural Product Research.
dc.identifier.doi10.1080/14786419.2025.2465605
dc.identifier.issn1478-6427
dc.identifier.issn1478-6419
dc.identifier.scopus2-s2.0-85218212142
dc.identifier.urihttps://hdl.handle.net/11449/308418
dc.language.isoeng
dc.relation.ispartofNatural Product Research
dc.sourceScopus
dc.subjectacylphoroglucinol
dc.subjectantibacterial
dc.subjectantifungal
dc.subjectdereplication
dc.subjectKielmeyera coriacea
dc.titleIntegrative dereplication and molecular networking reveal potential antimicrobial agents in Kielmeyera coriacea Mart.en
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0002-9597-1322[1]
unesp.author.orcid0000-0001-7109-9106[2]
unesp.author.orcid0000-0002-7244-5581[3]
unesp.author.orcid0009-0008-6092-2652[4]
unesp.author.orcid0009-0000-8587-0803[5]
unesp.author.orcid0000-0002-6710-6139[6]
unesp.author.orcid0000-0002-2793-9021[7]
unesp.author.orcid0000-0002-4471-4393[8]
unesp.author.orcid0000-0001-8634-6878[9]
unesp.author.orcid0000-0001-5384-6657[10]

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