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      <dc:title>A comparative study of the antiangiogenic activity of hydroxytyrosyl alkyl ethers</dc:title>
      <dc:creator>Marrero Capitán, Ana Dácil</dc:creator>
      <dc:creator>Castilla, Laura</dc:creator>
      <dc:creator>Espartero Sánchez, José Luis</dc:creator>
      <dc:creator>Madrona, Andrés</dc:creator>
      <dc:creator>Rodríguez-Quesada, Ana María</dc:creator>
      <dc:creator>Medina-Torres, Miguel Ángel</dc:creator>
      <dc:creator>Martínez-Póveda, Beatriz Amparo</dc:creator>
      <dc:subject>Neovascularización</dc:subject>
      <dc:subject>Aceite de oliva</dc:subject>
      <dc:description>Versión preprint del manuscrito de los autores, publicado finalmente en: Food Chemistry 333 (2020) 127476 con DOI: 10.1016/j.foodchem.2020.127476</dc:description>
      <dc:description>The phenolic compound hydroxytyrosol and its derivatives are responsible for some of the health benefits of the&#xd;
intake of virgin olive oil, having shown antiangiogenic properties. In this study, we explored the antiangiogenic&#xd;
potential of six synthetic hydroxytyrosyl alkyl ethers (HT C1, C2, C4, C6, C8 and C12). Our results showed that&#xd;
all compounds affected endothelial cell viability in vitro at low micromolar doses. In addition, compounds HT C1,&#xd;
C2, C4 and C6 inhibited endothelial cell migration and formation of tubular-like structures. In these assays,&#xd;
hydroxytyrosyl hexyl ether (HT C6) exhibited the most potent inhibitory activity in vitro, activating as well&#xd;
apoptosis in endothelial cells. Furthermore, the antiangiogenic activity of HT C6 was confirmed in vivo in the&#xd;
chick chorioallantoic membrane assay. Hence, we present hydroxytyrosol synthetic derivative HT C6 as a new&#xd;
antiangiogenic compound and as a good candidate for an antiangiogenic drug in the treatment of angiogenesisdependent&#xd;
diseases.</dc:description>
      <dc:date>2020-09-22T10:10:29Z</dc:date>
      <dc:date>2020-09-22T10:10:29Z</dc:date>
      <dc:date>2020-09</dc:date>
      <dc:date>2020-09-22</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>https://hdl.handle.net/10630/19821</dc:identifier>
      <dc:identifier>10.1016/j.foodchem.2020.127476</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
      <dc:rights>open access</dc:rights>
      <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
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