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    Pole DCWartośćJęzyk
    dc.contributor.authorBeata Godlewska-Żyłkiewicz, Beata-
    dc.contributor.authorŚwisłocka, Renata-
    dc.contributor.authorKalinowska, Monika-
    dc.contributor.authorGolonko, Aleksandra-
    dc.contributor.authorŚwiderski, Grzegorz-
    dc.contributor.authorArciszewska, Żaneta-
    dc.contributor.authorNalewajko-Sieliwoniuk, Edyta-
    dc.contributor.authorNaumowicz, Monika-
    dc.contributor.authorLewandowski, Włodzimierz-
    dc.date.accessioned2023-05-24T11:03:39Z-
    dc.date.available2023-05-24T11:03:39Z-
    dc.date.issued2020-
    dc.identifier.citationMaterials, Volume 13 Issue 19 (2020), p. 1-37pl
    dc.identifier.issn1996-1944-
    dc.identifier.urihttp://hdl.handle.net/11320/15006-
    dc.description.abstractNatural carboxylic acids are plant-derived compounds that are known to possess biological activity. The aim of this review was to compare the effect of structural differences of the selected carboxylic acids (benzoic acid (BA), cinnamic acid (CinA), p-coumaric acid (p-CA), caffeic acid (CFA), rosmarinic acid (RA), and chicoric acid (ChA)) on the antioxidant, antimicrobial, and cytotoxic activity. The studied compounds were arranged in a logic sequence of increasing number of hydroxyl groups and conjugated bonds in order to investigate the correlations between the structure and bioactivity. A review of the literature revealed that RA exhibited the highest antioxidant activity and this property decreased in the following order: RA > CFA ~ ChA > p-CA > CinA > BA. In the case of antimicrobial properties, structure-activity relationships were not easy to observe as they depended on the microbial strain and the experimental conditions. The highest antimicrobial activity was found for CFA and CinA, while the lowest for RA. Taking into account anti-cancer properties of studied NCA, it seems that the presence of hydroxyl groups had an influence on intermolecular interactions and the cytotoxic potential of the molecules, whereas the carboxyl group participated in the chelation of endogenous transition metal ions.pl
    dc.description.sponsorshipThis work was financially supported by National Science Centre, Poland, under the research project number 2018/29/B/NZ9/01997.pl
    dc.language.isoenpl
    dc.publisherMDPIpl
    dc.rightsUznanie autorstwa 4.0 Międzynarodowe*
    dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
    dc.subjectphenolic acidspl
    dc.subjectnatural carboxylic acidspl
    dc.subjectstructure-activity relationshippl
    dc.subjecthydroxyl groupspl
    dc.subjectantibacterialpl
    dc.subjectantioxidantpl
    dc.subjectcytotoxic activitypl
    dc.titleBiologically Active Compounds of Plants: Structure-Related Antioxidant, Microbiological and Cytotoxic Activity of Selected Carboxylic Acidspl
    dc.typeArticlepl
    dc.rights.holder© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) licensepl
    dc.identifier.doi10.3390/ma13194454-
    dc.description.AffiliationBeata Godlewska-Żyłkiewicz - Department of Analytical Chemistry, Faculty of Chemistry, University of Bialystokpl
    dc.description.AffiliationRenata Świsłocka - Department of Chemistry, Biology and Biotechnology, Bialystok University of Technologypl
    dc.description.AffiliationMonika Kalinowska - Department of Chemistry, Biology and Biotechnology, Bialystok University of Technologypl
    dc.description.AffiliationAleksandra Golonko - Institute of Agricultural and Food Biotechnology, Warsawpl
    dc.description.AffiliationGrzegorz Świderski - Department of Chemistry, Biology and Biotechnology, Bialystok University of Technologypl
    dc.description.AffiliationŻaneta Arciszewska - Department of Analytical Chemistry, Faculty of Chemistry, University of Bialystokpl
    dc.description.AffiliationEdyta Nalewajko-Sieliwoniuk - Department of Analytical Chemistry, Faculty of Chemistry, University of Bialystokpl
    dc.description.AffiliationMonika Naumowicz - Department of Physical Chemistry, Faculty of Chemistry, University of Bialystokpl
    dc.description.AffiliationWłodzimierz Lewandowski - Department of Chemistry, Biology and Biotechnology, Bialystok University of Technologypl
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