Detalle Publicación

ARTÍCULO
Design, Synthesis, and Biological Evaluation of First-in-Class Dual Acting Histone Deacetylases (HDACs) and Phosphodiesterase 5 (PDE5) Inhibitors for the Treatment of Alzheimer's Disease
Autores: Rabal Gracia, María Obdulia; Sánchez-Arias, J. A.; Cuadrado Tejedor, María del Mar; De Miguel, I. ; Pérez-González, M.; Garcia Barroso, Carolina; Ugarte, A. ; Estella Hermoso de Mendoza, Ander; Sáez de Blas, Elena; Espelosín Azpilicueta, María; Ursua, S. ; Haizhong, T. ; Wei, W. ; Musheng, X. ; García Osta, Ana María; Oyarzabal Santamarina, Julen
Título de la revista: JOURNAL OF MEDICINAL CHEMISTRY
ISSN: 0022-2623
Volumen: 59
Número: 19
Páginas: 8967-9004
Fecha de publicación: 2016
Resumen:
Simultaneous inhibition of phosphodiesterase 5 (PDE5) and histone deacetylases (HDAC) has recently been validated as a potentially novel therapeutic approach for Alzheimer's disease (AD). To further extend this concept, we designed and synthesized the first chemical series of dual acting PDE5 and HDAC inhibitors, and we validated this systems therapeutics approach. Following the implementation of structure- and knowledge-based approaches, initial hits were designed and were shown to validate our hypothesis of dual in vitro inhibition. Then, an optimization strategy was pursued to obtain a proper tool compound for in vivo testing in AD models. Initial hits were translated into molecules with adequate cellular functional responses (histone acetylation and cAMP/cGMP response element-binding (CREB) phosphorylation in the nanomolar range), an acceptable therapeutic window (>1 log unit), and the ability to cross the blood-brain barrier, leading to the identification of 7 as a candidate for in vivo proof-of-concept testing ( Cuadrado-Tejedor, M.; Garcia-Barroso, C.; Sánchez-Arias, J. A.; Rabal, O.; Mederos, S.; Ugarte, A.; Franco, R.; Segura, V.; Perea, G.; Oyarzabal, J.; Garcia-Osta, A. Neuropsychopharmacology 2016 , in press, doi: 10.1038/npp.2016.163 ).