Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10591313 | Bioorganic & Medicinal Chemistry Letters | 2013 | 22 Pages |
Abstract
The metabotropic glutamate receptor subtype 5 has evolved into a promising target for the treatment of various diseases of the central nervous system, such as Fragile X and l-DOPA induced dyskinesia. One of the most advanced clinical compound is Novartis' AFQ-056 (Mavoglurant), which served us as a template for a scaffold hopping approach, generating a structurally diverse set of potent analogs. Both the limited aqueous solubility and the relatively poor metabolic stability of AFQ-056 were improved with hexahydrocyclopenta[c]pyrrole derivative 54a, which proved to be a valuable candidate for further development.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Holger Kubas, Udo Meyer, Mirko Hechenberger, Kai-Uwe Klein, Patrick Plitt, Ronalds Zemribo, Harm W. Spexgoor, Sander G.A. van Assema, Ulrich Abel,