<?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>2026-05-30T11:39:36Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/28119" metadataPrefix="qdc">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><qdc:qualifieddc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <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>
   <dcterms:abstract>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;
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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).</dcterms:abstract>
   <dcterms:dateAccepted>2023-11-23T07:48:02Z</dcterms:dateAccepted>
   <dcterms:available>2023-11-23T07:48:02Z</dcterms:available>
   <dcterms:created>2023-11-23T07:48:02Z</dcterms:created>
   <dcterms:issued>2023</dcterms:issued>
   <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>
</qdc:qualifieddc>
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