Logo do repositório

Traditional Use, Chemical Constituents, and Pharmacological Activity of Maytenus elaeodendroides Stem Bark

dc.contributor.authorGarcía, Trina H.
dc.contributor.authorSpengler, Iraida
dc.contributor.authorFernández, Antonio
dc.contributor.authorRodeiro, Idania
dc.contributor.authorHernández-Balmaseda, Ivones
dc.contributor.authorCéspedes, Ilianet
dc.contributor.authorGarrido, Gabino
dc.contributor.authordos Santos, Lourdes Campaner [UNESP]
dc.contributor.authorVilegas, Wagner [UNESP]
dc.contributor.authorCelano, Rita
dc.contributor.authorD’Elia, Maria
dc.contributor.institutionUniversity of Havana
dc.contributor.institutionInstitute of Marine Sciences (ICIMAR)
dc.contributor.institutionUniversidad de Católica del Norte
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversity of Salerno
dc.contributor.institutionNational Biodiversity Future Center
dc.date.accessioned2025-04-29T18:49:32Z
dc.date.issued2024-11-01
dc.description.abstractPlants belonging to the genus Maytenus are members of the Celastraceae family. They have been widely used by different peoples as treatment for curing many diseases. The aim of this study was to explore the anti-inflammatory and antioxidant properties of Maytenus elaeodendroides stem bark extracts, an endemic Cuban plant. The antioxidant activity of four extracts (EtOH, EtOAc, n-BuOH, and diethyl ether/petroleum ether 1:1) was determined using DPPH and FRAP methods. Meanwhile, anti-inflammatory effects by the edema method were induced by croton oil in the mouse ear. The investigated extracts showed radical reduction capacity and prevented ear inflammation at doses of 4 mg/ear. In addition, FIA/ESI/IT/MSn was used to determine the qualitative chemical composition of the EtOAc extract and allowed the identification of five flavan-3-ol monomers, four dimers, and other proanthocyanidin oligomers. From this extract three flavan-3-ol compounds (elaeocyanidin and 4′-O-methylgallocatechin), one of them new (2′-hydroxy-4′-methoxy-epigallocatechin), and a proanthocyanidin dimer (afzelechin-((Formula presented.))-4′-O-methylepigallocatechin) were isolated and identified by the chromatographic method and spectroscopic techniques, mainly ESI-MS and NMR spectroscopic methods.en
dc.description.affiliationCenter for Natural Product Research Faculty of Chemistry University of Havana
dc.description.affiliationPharmacology Department Institute of Marine Sciences (ICIMAR), Loma 14, Alturas del Vedado, Plaza de la Revolución
dc.description.affiliationDepartment of Pharmaceutical Sciences Faculty of Sciences Universidad de Católica del Norte, Angamos 0610
dc.description.affiliationDepartment of Organic Chemistry Institute of Chemistry UNESP—Sao Paulo State University, Araraquara
dc.description.affiliationExperimental Campus of Sao Vicente UNESP—Sao Paulo State University, Sao Paulo
dc.description.affiliationDipartimento di Farmacia University of Salerno
dc.description.affiliationNBFC National Biodiversity Future Center
dc.description.affiliationUnespDepartment of Organic Chemistry Institute of Chemistry UNESP—Sao Paulo State University, Araraquara
dc.description.affiliationUnespExperimental Campus of Sao Vicente UNESP—Sao Paulo State University, Sao Paulo
dc.identifierhttp://dx.doi.org/10.3390/d16110694
dc.identifier.citationDiversity, v. 16, n. 11, 2024.
dc.identifier.doi10.3390/d16110694
dc.identifier.issn1424-2818
dc.identifier.scopus2-s2.0-85210526224
dc.identifier.urihttps://hdl.handle.net/11449/300421
dc.language.isoeng
dc.relation.ispartofDiversity
dc.sourceScopus
dc.subject2′-hydroxy-4′-methoxy-epigallocatechin
dc.subjectantioxidant and anti-inflammatory activity
dc.subjectFIA/ESI/IT/MSn
dc.subjectflavan-3-ol
dc.subjectMaytenus elaeodendroides
dc.subjectproanthocyanidins
dc.titleTraditional Use, Chemical Constituents, and Pharmacological Activity of Maytenus elaeodendroides Stem Barken
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.author.orcid0000-0002-4044-0567[1]
unesp.author.orcid0000-0002-2692-6050[4]
unesp.author.orcid0000-0001-5276-0851[5]
unesp.author.orcid0000-0003-3032-2556[9]
unesp.author.orcid0000-0002-6357-594X[10]
unesp.author.orcid0009-0009-5315-3055[11]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Câmpus Experimental do Litoral Paulista, São Vicentept

Arquivos