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Detalle de: Modulation of cAMP-Specific PDE without Emetogenic Activity: New Sulfide-Like PDE7 Inhibitors

Title Modulation of cAMP-Specific PDE without Emetogenic Activity: New Sulfide-Like PDE7 Inhibitors
Abstract

A forward chemical genetic approach was followed to discover new targets and lead compounds for Parkinson’s disease (PD) treatment. By analysis of the cell protection produced by some small molecules, a diphenyl sulfide compound was revealed to be a new phosphodiesterase 7 (PDE7) inhibitor and identified as a new hit. This result allows us to confirm the utility of PDE7 inhibitors as a potential pharmacological treatment of PD. On the basis of these data, a diverse family of diphenyl sulfides has been developed and pharmacologically evaluated in the present work. Moreover, to gain insight into the safety of PDE7 inhibitors for human chronic treatment, we evaluated the new compounds in a surrogate emesis model, showing nonemetic effects.

Apa Reference García, A. M., Brea, J., Morales-García, J. A., Perez, D. I., González, A., Alonso-Gil, S., Gracia-Rubio, I., Ros-Simó, C., Conde, S., Cadavid, M. I., Loza, M. I., Perez-Castillo, A., Valverde, O., Martinez, A., & Gil, C. (2014). Modulation of cAMP-Specific PDE without Emetogenic Activity: New Sulfide-Like PDE7 Inhibitors. Journal of Medicinal Chemistry, 57(20), 8590–8607. 10.1021/jm501090m
Doi 10.1021/jm501090m
Publication Date 29 Sep 2014
Publication Type Article
Researcher Ana Martínez
Ontology Drug Discovery and design
Research Groups Translational Medicinal and Biological Chemistry
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