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The emerging role of mixed lineage kinase 3 (MLK3) and its potential as a target for neurodegenerative diseases therapies

dc.contributor.authorMoreno, Ricardo
dc.contributor.authorRecio, Javier
dc.contributor.authorBarber, Santiago
dc.contributor.authorGil, Carmen
dc.contributor.authorMartinez, Ana
dc.date.accessioned2024-01-26T10:22:01Z
dc.date.available2024-01-26T10:22:01Z
dc.date.issued2023-05-24
dc.identifier.citationEuropean Journal of Medicinal Chemistry 257 (2023) 115511es
dc.identifier.urihttps://hdl.handle.net/10115/28970
dc.description.abstractSelective and brain-permeable protein kinase inhibitors are in preclinical development for treating neurodegenerative diseases. Among them, MLK3 inhibitors, with a potent neuroprotective biological action have emerged as valuable agents for the treatment of pathologies such as Alzheimer’s, Parkinson’s disease and amyotrophic lateral sclerosis. In fact, one MLK3 inhibitor, CEP-1347, reached clinical trials for Parkinson’s disease. Additionally, another compound called prostetin/12k, a potent and rather selective MLK3 inhibitor has started clinical development for ALS based on its motor neuron protection in both in vitro and in vivo models. In this review, we will focus on the role of MLK3 in neuron-related cell death processes, neurodegenerative diseases, and the potential advantages of targeting this kinase through pharmacological modulation for neuroprotective treatment.es
dc.language.isoenges
dc.publisherELSERVIERes
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectMLK3es
dc.subjectProtein kinase inhibitorses
dc.subjectNeurodegenerative diseaseses
dc.titleThe emerging role of mixed lineage kinase 3 (MLK3) and its potential as a target for neurodegenerative diseases therapieses
dc.typeinfo:eu-repo/semantics/reviewes
dc.identifier.doi10.1016/j.ejmech.2023.115511es
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses


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Atribución 4.0 InternacionalExcept where otherwise noted, this item's license is described as Atribución 4.0 Internacional