| Literature DB >> 28548834 |
Valle Palomo1, Daniel I Perez1, Carlos Roca1, Cara Anderson2, Natalia Rodríguez-Muela3, Concepción Perez4, Jose A Morales-Garcia5,6, Julio A Reyes4, Nuria E Campillo1, Ana M Perez-Castillo5,6, Lee L Rubin3, Lubov Timchenko2, Carmen Gil1, Ana Martinez1.
Abstract
Glycogen synthase kinase 3 β (GSK-3β) is a central target in several unmet diseases. To increase the specificity of GSK-3β inhibitors in chronic treatments, we developed small molecules allowing subtle modulation of GSK-3β activity. Design synthesis, structure-activity relationships, and binding mode of quinoline-3-carbohydrazide derivatives as allosteric modulators of GSK-3β are presented here. Furthermore, we show how allosteric binders may overcome the β-catenin side effects associated with strong GSK-3β inhibition. The therapeutic potential of some of these modulators has been tested in human samples from patients with congenital myotonic dystrophy type 1 (CDM1) and spinal muscular atrophy (SMA) patients. We found that compound 53 improves delayed myogenesis in CDM1 myoblasts, while compounds 1 and 53 have neuroprotective properties in SMA-derived cells. These findings suggest that the allosteric modulators of GSK-3β may be used for future development of drugs for DM1, SMA, and other chronic diseases where GSK-3β inhibition exhibits therapeutic effects.Entities:
Mesh:
Substances:
Year: 2017 PMID: 28548834 DOI: 10.1021/acs.jmedchem.7b00395
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446