<?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>2026-06-01T16:04:25Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/28119" metadataPrefix="rdf">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/28119</identifier><datestamp>2026-02-03T12:28:13Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37959</setSpec></header><metadata><rdf:RDF xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:ds="http://dspace.org/ds/elements/1.1/" xmlns:ow="http://www.ontoweb.org/ontology/1#" xmlns:rdf="http://www.openarchives.org/OAI/2.0/rdf/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/rdf/ http://www.openarchives.org/OAI/2.0/rdf.xsd">
   <ow:Publication rdf:about="oai:riuma.uma.es:10630/28119">
      <dc:title>Glycomimetic Ligands for C-type Lectin Recognition.</dc:title>
      <dc:creator>Luna León, Rubén</dc:creator>
      <dc:creator>Reina Martín, José Juan</dc:creator>
      <dc:subject>Lectinas</dc:subject>
      <dc:subject>Ligandos</dc:subject>
      <dc:subject>Química orgánica</dc:subject>
      <dc:description>C-type lectin receptors (CLRs) represent pivotal sensory mechanisms orchestrating the primary immune response via dendritic cells.1 The exploration of non-native ligands as molecular tools for the manipulation of CLRs has emerged as a highly interesting research area. In the case of DC-SIGN, one of the most extensively investigated CLRs, glycomimetics have been formulated as principal compounds with a demonstrated capacity to proficiently engage DC-SIGN (Figure 1 and 2). The principal problem encountered refers to the structural complexity and challenging synthetic processes associated with these glycomimetics.&#xd;
&#xd;
In this context, we introduce a novel class of glycomimetic ligands designed for DC-SIGN that exhibit a simpler structural composition and can be readily synthesized. These ligands hold significant promise for potential applications in the field of immune regulation therapeutic (Figure 3).</dc:description>
      <dc:date>2023-11-23T07:48:02Z</dc:date>
      <dc:date>2023-11-23T07:48:02Z</dc:date>
      <dc:date>2023</dc:date>
      <dc:type>conference output</dc:type>
      <dc:identifier>https://hdl.handle.net/10630/28119</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>XIX Simposio de Jóvenes Investigadores Químicos de la RSEQ</dc:relation>
      <dc:relation>Murcia</dc:relation>
      <dc:relation>13-11-2023/16-11-2023</dc:relation>
      <dc:rights>open access</dc:rights>
   </ow:Publication>
</rdf:RDF>
</metadata></record></GetRecord></OAI-PMH>