Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/11000/39585

Brain Permeable SGK1 Inhibitors: A Promising Therapeutic Strategy for Neurodegenerative Diseases


thumbnail_pdf
Ver/Abrir:
 SGK1.pdf

6,22 MB
Adobe PDF
Compartir:
Título :
Brain Permeable SGK1 Inhibitors: A Promising Therapeutic Strategy for Neurodegenerative Diseases
Autor :
Madruga, Enrique
García-Rubia, Alfonso
Sánchez-Núñez, Carlos
Martínez-González, Loreto
Fernández-Escamilla, Ana María
Lastres-Becker, Isabel
Gil, Carmen
Martínez, Ana
Editor :
American Chemical Society
Departamento:
Departamentos de la UMH::Bioquímica y Biología Molecular
Fecha de publicación:
2025-10
URI :
https://hdl.handle.net/11000/39585
Resumen :
A major challenge in modern medicine is developing new therapies for aging-related diseases such as neurodegenerative disorders, whose prevalence increases with longer life expectancy. Although kinase inhibitors have achieved clinical success, their development for central nervous system (CNS) disorders remains limited due to the complexity of kinase networks and poor blood− brain barrier (BBB) permeability. Serum/glucocorticoid-regulated kinase 1 (SGK1) participates in multiple signaling pathways but remains an underexplored target in neurodegeneration. Following a mixed ligand- and structure-based virtual screening, we have previously identified a brain-penetrant SGK1 inhibitor. A medicinal chemistry program based on hit expansion and optimization for BBB permeability reported here has generated a new family of SGK1 inhibitors as chemical probes that enable the investigation of SGK1’s role in neurological disorders and serve as promising starting points for drug development. These findings highlight SGK1 as a potential therapeutic target for neurodegenerative diseases, such as Alzheimer’s disease.
Palabras clave/Materias:
SGK1
neurodegeneration
kinase inhibitors
neurodegenerative diseases
Área de conocimiento :
CDU: Ciencias puras y naturales: Biología: Bioquímica. Biología molecular. Biofísica
Tipo de documento :
info:eu-repo/semantics/article
Derechos de acceso:
info:eu-repo/semantics/openAccess
Attribution-NonCommercial-NoDerivatives 4.0 Internacional
DOI :
https://doi.org/10.1021/acs.jmedchem.5c03050
Publicado en:
Journal of Medicinal Chemistry - (ASAP) (2026)
Aparece en las colecciones:
Artículos - Bioquímica y Biología Molecular



Creative Commons La licencia se describe como: Atribución-NonComercial-NoDerivada 4.0 Internacional.