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            <description>A name given to the resource</description>
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                <text>Coronavirus</text>
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            <description>An account of the resource</description>
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                <text>Dominio científico: Coronavirus</text>
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          <name>Title</name>
          <description>A name given to the resource</description>
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              <text>The Impact of O-Glycosylation on Cyanidin Interaction with POPC Membranes: Structure-Activity Relationship</text>
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          <name>Creator</name>
          <description>An entity primarily responsible for making the resource</description>
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              <text>Sylwia Cyboran-Mikołajczyk, Piotr Jurkiewicz, Martin Hof, Halina Kleszczyńska</text>
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          <name>Description</name>
          <description>An account of the resource</description>
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              <text>Cyanidin and its O-glycosides have many important physiological functions in plants and beneficial effects on human health. Their biological activity is not entirely clear and depends on the structure of the molecule, in particular, on the number and type of sugar substituents. Therefore, in this study the detailed structure-activity relationship (SARs) of the anthocyanins/anthocyanidins in relation to their interactions with lipid bilayer was determined. On the basis of their antioxidant activity and the changes induced by them in size and Zeta potential of lipid vesicles, and mobility and order of lipid acyl chains, the impact of the number and type of sugar substituents on the biological activity of the compounds was evaluated. The obtained results have shown, that 3-O-glycosylation changes the interaction of cyanidin with lipid bilayer entirely. The 3-O-glycosides containing a monosaccharide induces greater changes in physical properties of the lipid membrane than those containing disaccharides. The presence of additional sugar significantly reduces glycoside interaction with model lipid membrane. Furthermore, O-glycosylation alters the ability of cyanidin to scavenge free radicals. This alteration depends on the type of free radicals and the sensitivity of the method used for their determination.</text>
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          <name>Date</name>
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              <text>2018</text>
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          <name>Subject</name>
          <description>The topic of the resource</description>
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              <text>structure-activity relationships, Lipid peroxidation, phospholipid membrane, Anthocya-nin, fluorescence dyes, hydrogen peroxide, membrane fluidity</text>
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          <name>Identifier</name>
          <description>An unambiguous reference to the resource within a given context</description>
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            <elementText elementTextId="11212">
              <text>DOI: 10.3390/molecules23112771</text>
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          <name>Source</name>
          <description>A related resource from which the described resource is derived</description>
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              <text>Molecules</text>
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          <name>Publisher</name>
          <description>An entity responsible for making the resource available</description>
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            <elementText elementTextId="11214">
              <text>MDPI AG</text>
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          <name>Coverage</name>
          <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
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            <elementText elementTextId="11215">
              <text>Organic chemistry</text>
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          <name>Language</name>
          <description>A language of the resource</description>
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              <text>EN</text>
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