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dc.contributor.authorGarcia-Carceles, Javieres_ES
dc.contributor.authorCaballero, Elenaes_ES
dc.contributor.authorGil, Carmenes_ES
dc.contributor.authorMartínez Gil, Anaes_ES
dc.date.accessioned2021-05-17T08:50:34Z-
dc.date.available2021-05-17T08:50:34Z-
dc.date.issued2021-05-10-
dc.identifier.citationJournal of Medicinal Chemistry (2021)es_ES
dc.identifier.issn0022-2623-
dc.identifier.urihttp://hdl.handle.net/10261/240925-
dc.description73 p.-12 fig.-1 tab.-1 graph. abst.es_ES
dc.description.abstractViral infections are a major health problem; therefore, there is an urgent need for novel therapeutic strategies.Antivirals used to target proteins encoded by the viral genome usually enhance drug resistance generated by the virus. A potentialsolution may be drugs acting at host-based targets since viruses are dependent on numerous cellular proteins and phosphorylationevents that are crucial during their life cycle. Repurposing existing kinase inhibitors as antiviral agents would help in the cost andeffectiveness of the process, but this strategy usually does not provide much improvement, and specific medicinal chemistryprograms are needed in thefield. Anyway, extensive use of FDA-approved kinase inhibitors has been quite useful in deciphering therole of host kinases in viral infection. The present perspective aims to review the state of the art of kinase inhibitors that target viralinfections in different development stages.es_ES
dc.description.sponsorshipFunding from“la Caixa”Banking Foundation (LCF/PR/HR19/52160012), CSIC (202020E103 and 202080E293),and AEI (Grant PID2019-105600RB-I00) is acknowledged.E.C. holds a JAE Intro fellowship (JAEINT_20_01339) from CSIC.es_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-105600RB-I00)es_ES
dc.rightsopenAccessen_EN
dc.titleKinase inhibitors as underexplored antiviral agentses_ES
dc.typeartículoes_ES
dc.identifier.doi10.1021/acs.jmedchem.1c00302-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1021/acs.jmedchem.1c00302es_ES
dc.identifier.e-issn1520-4804-
dc.description.versionpostprint-
dc.contributor.funderLa Caixaes_ES
dc.contributor.funderConsejo Superior de Investigaciones Científicas (España)es_ES
dc.contributor.funderAgencia Estatal de Investigación (España)es_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003339es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100011033es_ES
dc.contributor.orcidGarcia-Carceles, Javier [0000-0003-4614-9639]es_ES
dc.contributor.orcidGil, Carmen [0000-0002-3882-6081]es_ES
dc.contributor.orcidMartínez, Ana [0000-0002-2707-8110]es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.grantfulltextopen-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeartículo-
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