<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-30T07:05:01Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/19821" metadataPrefix="mods">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/19821</identifier><datestamp>2026-02-03T11:00:56Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37953</setSpec></header><metadata><mods:mods xmlns:doc="http://www.lyncode.com/xoai" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
   <mods:name>
      <mods:namePart>Marrero Capitán, Ana Dácil</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Castilla, Laura</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Espartero Sánchez, José Luis</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Madrona, Andrés</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Rodríguez-Quesada, Ana María</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Medina-Torres, Miguel Ángel</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Martínez-Póveda, Beatriz Amparo</mods:namePart>
   </mods:name>
   <mods:extension>
      <mods:dateAvailable encoding="iso8601">2020-09-22T10:10:29Z</mods:dateAvailable>
   </mods:extension>
   <mods:extension>
      <mods:dateAccessioned encoding="iso8601">2020-09-22T10:10:29Z</mods:dateAccessioned>
   </mods:extension>
   <mods:originInfo>
      <mods:dateIssued encoding="iso8601">2020-09-22</mods:dateIssued>
   </mods:originInfo>
   <mods:identifier type="uri">https://hdl.handle.net/10630/19821</mods:identifier>
   <mods:identifier type="doi">10.1016/j.foodchem.2020.127476</mods:identifier>
   <mods:abstract>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.</mods:abstract>
   <mods:language>
      <mods:languageTerm>eng</mods:languageTerm>
   </mods:language>
   <mods:accessCondition type="useAndReproduction">http://creativecommons.org/licenses/by-nc-nd/4.0/</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">open access</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">Attribution-NonCommercial-NoDerivatives 4.0 Internacional</mods:accessCondition>
   <mods:subject>
      <mods:topic>Neovascularización</mods:topic>
   </mods:subject>
   <mods:subject>
      <mods:topic>Aceite de oliva</mods:topic>
   </mods:subject>
   <mods:titleInfo>
      <mods:title>A comparative study of the antiangiogenic activity of hydroxytyrosyl alkyl ethers</mods:title>
   </mods:titleInfo>
   <mods:genre>journal article</mods:genre>
</mods:mods>
</metadata></record></GetRecord></OAI-PMH>