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GSK-3β Allosteric Inhibition: A Dead End or a New Pharmacological Frontier?
Most kinase inhibitors are designed to bind to highly homologous ATP-binding sites, which leads to promiscuity and possible off-target effects. Allostery is an alternative approach to pursuing selectivity. However, allostery is difficult to exploit due to the wide variety of underlying mechanisms an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10139115/ https://www.ncbi.nlm.nih.gov/pubmed/37108703 http://dx.doi.org/10.3390/ijms24087541 |