Scaffold hopping approach towards various AFQ-056 analogs as potent metabotropic glutamate receptor 5 negative allosteric modulators

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...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2013-12, Vol.23 (23), p.6370-6376
Hauptverfasser: Kubas, Holger, Meyer, Udo, Hechenberger, Mirko, Klein, Kai-Uwe, Plitt, Patrick, Zemribo, Ronalds, Spexgoor, Harm W., van Assema, Sander G.A., Abel, Ulrich
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Sprache:eng
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Zusammenfassung: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.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2013.09.059