<?xml version="1.0"?><rdf:RDF xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:edm="http://www.europeana.eu/schemas/edm/" xmlns:wgs84_pos="http://www.w3.org/2003/01/geo/wgs84_pos" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:rdaGr2="http://rdvocab.info/ElementsGr2" xmlns:oai="http://www.openarchives.org/OAI/2.0/" xmlns:owl="http://www.w3.org/2002/07/owl#" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:ore="http://www.openarchives.org/ore/terms/" xmlns:skos="http://www.w3.org/2004/02/skos/core#" xmlns:dcterms="http://purl.org/dc/terms/"><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:DOC-JEMGSAXO/16c3354d-680f-4ec8-be47-6391b4de885c/PDF"><dcterms:extent>249 KB</dcterms:extent></edm:WebResource><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:DOC-JEMGSAXO/f96604ef-9e2c-492e-bb26-5fbcd7881d24/TEXT"><dcterms:extent>52 KB</dcterms:extent></edm:WebResource><edm:TimeSpan rdf:about="1998-2025"><edm:begin xml:lang="en">1998</edm:begin><edm:end xml:lang="en">2025</edm:end></edm:TimeSpan><edm:ProvidedCHO rdf:about="URN:NBN:SI:DOC-JEMGSAXO"><dcterms:isPartOf rdf:resource="https://www.dlib.si/details/URN:NBN:SI:spr-KC6O72BG" /><dcterms:issued>2013</dcterms:issued><dc:creator>Gašperlin, Mirjana</dc:creator><dc:creator>Gosenca, Mirjam</dc:creator><dc:creator>Mravljak, Janez</dc:creator><dc:creator>Obreza, Aleš</dc:creator><dc:format xml:lang="sl">številka:2</dc:format><dc:format xml:lang="sl">letnik:60</dc:format><dc:format xml:lang="sl">str. 310-322</dc:format><dc:identifier>ISSN:1318-0207</dc:identifier><dc:identifier>COBISSID:3475313</dc:identifier><dc:identifier>URN:URN:NBN:SI:doc-JEMGSAXO</dc:identifier><dc:language>en</dc:language><dc:publisher xml:lang="sl">Slovenian Chemical Society</dc:publisher><dc:publisher xml:lang="sl">Slovensko kemijsko društvo</dc:publisher><dcterms:isPartOf xml:lang="sl">Acta chimica slovenica</dcterms:isPartOf><dc:subject xml:lang="sl">amfifilne spojine</dc:subject><dc:subject xml:lang="en">amhiphilic molecules</dc:subject><dc:subject xml:lang="en">amidoximes</dc:subject><dc:subject xml:lang="sl">antioksidanti</dc:subject><dc:subject xml:lang="en">antioxidant</dc:subject><dc:subject xml:lang="en">antioxidant activity</dc:subject><dc:subject xml:lang="sl">benzoksimi</dc:subject><dc:subject xml:lang="sl">dimeri oksimov</dc:subject><dc:subject xml:lang="sl">DPPH metoda</dc:subject><dc:subject xml:lang="en">glycolipid mimetics</dc:subject><dc:subject xml:lang="sl">oksimski derivati glikolipidnih mimetikov</dc:subject><dc:subject xml:lang="en">oximes</dc:subject><dc:subject xml:lang="sl">sinteza</dc:subject><dc:subject xml:lang="sl">stabilnost farmacevtskih učinkovin</dc:subject><dcterms:temporal rdf:resource="1998-2025" /><dc:title xml:lang="sl">The design, synthesis, and antioxidant activity of amphiphilic oximes and amidoximes|</dc:title><dc:description xml:lang="sl">New amphiphilic benzamidoxime, benzoxime, and aliphatic oxime derivatives of glycolipid mimetics were synthesized. The total antioxidant capacity of these amphiphilic derivatives was evaluated using DPPH assay. The observed antioxidant activity was the highest for benzamidoxime derivatives and glycolipid mimetics with two oxime functionalities, followed by benzoxime derivatives, glycolipid mimetics with one oxime group, and dimers of oxime. Due to their amphiphilic structure, which was a guidance for compound design and synthesis, these novel amphiphilic compounds can be proposed as potential antioxidants for tackling oxidative processes in two-phase systems, either biological (cell membranes) or artificial (emulsions)</dc:description><dc:description xml:lang="sl">Sintetizirali smo nove amfifilne spojine benzamidoksimskega in benzoksimskega tipa ter oksimske derivate glikolipidnih mimetikov z alkilno verigo. Celokupno antioksidativno kapaciteto amfifilnih derivatov smo ovrednotili z DPPH metodo. Benzamidoksimi in glikolipidni mimetiki z dvema oksimskima skupinama imajo najmočnejše antioksidativno delovanje, sledijo jim benzoksimski derivati, glikolipidni mimetiki z eno oksimsko skupino ter dimerioksimov. Zaradi amfifilne strukture, ki je bila vodilo pri načrtovanju in sintezi, bi nove sintetizirane amfifilne spojine lahko uporabili kot potencialne antioksidante za omejitev oksidativnih procesov v dvofaznih sistemih, tako bioloških (celične membrane) kot umetnih (emulzije)</dc:description><edm:type>TEXT</edm:type><dc:type xml:lang="sl">znanstveno časopisje</dc:type><dc:type xml:lang="en">journals</dc:type><dc:type rdf:resource="http://www.wikidata.org/entity/Q361785" /></edm:ProvidedCHO><ore:Aggregation rdf:about="http://www.dlib.si/?URN=URN:NBN:SI:DOC-JEMGSAXO"><edm:aggregatedCHO rdf:resource="URN:NBN:SI:DOC-JEMGSAXO" /><edm:isShownBy rdf:resource="http://www.dlib.si/stream/URN:NBN:SI:DOC-JEMGSAXO/16c3354d-680f-4ec8-be47-6391b4de885c/PDF" /><edm:rights rdf:resource="http://creativecommons.org/licenses/by/4.0/" /><edm:provider>Slovenian National E-content Aggregator</edm:provider><edm:intermediateProvider xml:lang="en">National and University Library of Slovenia</edm:intermediateProvider><edm:dataProvider xml:lang="sl">Slovensko kemijsko društvo</edm:dataProvider><edm:object rdf:resource="http://www.dlib.si/streamdb/URN:NBN:SI:DOC-JEMGSAXO/maxi/edm" /><edm:isShownAt rdf:resource="http://www.dlib.si/details/URN:NBN:SI:DOC-JEMGSAXO" /></ore:Aggregation></rdf:RDF>