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Publicação:
Advanced Glycation End Product Inhibition by Alkaloids from Ocotea paranapiacabensis for the Prevention of Skin Aging

dc.contributor.authorFreitas, Larissa De [UNESP]
dc.contributor.authorValli, Marilia [UNESP]
dc.contributor.authorDametto, Alessandra C. [UNESP]
dc.contributor.authorPennacchi, Paula C.
dc.contributor.authorAndricopulo, Adriano D.
dc.contributor.authorMaria-Engler, Silvya S.
dc.contributor.authorBolzani, Vanderlan S. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionNo. 625
dc.date.accessioned2020-12-12T01:59:18Z
dc.date.available2020-12-12T01:59:18Z
dc.date.issued2020-01-01
dc.description.abstractA bioassay-guided study aiming at identifying inhibitors of the glycation process on the leaves of Ocotea paranapiacabensis afforded four benzylisoquinoline alkaloids (1-4), with 1 and 2 identified as new naturals products, while 3 and 4 were previously described in the literature, with 3 being identified as magnocurarine. Purification was performed by column chromatography and high-performance liquid chromatography. The structures of the isolated compounds were elucidated by spectroscopic methods including UV, NMR, and HRMS. The process of skin aging has been recently associated with advanced glycation end products (AGEs), and strategies inhibiting their formation have been addressed by pharmaceutical companies for the development of novel antiaging compounds. Alkaloids 1-4 were evaluated for their potential to inhibit AGE formation and showed inhibition of 62.9%, 83.3%, 26.1%, and 98.2% (150 μM), respectively. The antiaging potential of compounds 1 and 4 were evaluated with a reconstructed human skin model in vitro, and results showed a decrease in dermis contraction (8.7% and 4.2% respectively for 1 and 4) when compared to the glycated control (57.4%). Additionally, absorption, distribution, metabolism, and excretion (ADME) and toxicity properties were predicted using in silico methods, and the results were considered significantly promising for alkaloids 1 and 4 to continue the development of these alkaloids with skincare properties.en
dc.description.affiliationNuclei of Bioassays Biosynthesis and Ecophysiology of Natural Products (NuBBE) Department of Organic Chemistry Institute of Chemistry Saõ Paulo State University (UNESP)
dc.description.affiliationLaboratory of Medicinal and Computational Chemistry (LQMC) Centre for Research and Innovation in Biodiversity and Drug Discovery (CIBFar) Institute of Physics of Saõ Carlos University of Saõ Paulo (USP)
dc.description.affiliationFederal Institute of Education Science and Technology of Saõ Paulo Rua Stéfano d'Avassi No. 625
dc.description.affiliationDepartment of Clinical and Toxicological Analysis Faculty of Pharmaceutical Sciences University of Saõ Paulo (USP)
dc.description.affiliationUnespNuclei of Bioassays Biosynthesis and Ecophysiology of Natural Products (NuBBE) Department of Organic Chemistry Institute of Chemistry Saõ Paulo State University (UNESP)
dc.identifierhttp://dx.doi.org/10.1021/acs.jnatprod.9b01083
dc.identifier.citationACS Applied Materials and Interfaces.
dc.identifier.doi10.1021/acs.jnatprod.9b01083
dc.identifier.issn1944-8252
dc.identifier.issn1944-8244
dc.identifier.scopus2-s2.0-85081646202
dc.identifier.urihttp://hdl.handle.net/11449/200163
dc.language.isoeng
dc.relation.ispartofACS Applied Materials and Interfaces
dc.sourceScopus
dc.titleAdvanced Glycation End Product Inhibition by Alkaloids from Ocotea paranapiacabensis for the Prevention of Skin Agingen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0003-1106-183X 0000-0003-1106-183X[2]
unesp.author.orcid0000-0002-0457-818X[5]
unesp.author.orcid0000-0001-7019-5825[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentQuímica Orgânica - IQARpt

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