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Benzimidazoles as Potent and Orally Active mGlu5 Receptor Antagonists with an Improved PK Profile
A focused chemical optimization effort of compound 1 based on metabolite elucidation is described, resulting in 15i, a highly potent and selective mGlu5 receptor antagonist with an improved pharmacokinetic profile compared to 1. Characterization of 15i in vivo in the fear-potentiated startle (FPS) p...
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Published in: | ACS medicinal chemistry letters 2011-01, Vol.2 (1), p.58-62 |
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creator | Carcache, David Vranesic, Ivo Blanz, Joachim Desrayaud, Sandrine Fendt, Markus Glatthar, Ralf |
description | A focused chemical optimization effort of compound 1 based on metabolite elucidation is described, resulting in 15i, a highly potent and selective mGlu5 receptor antagonist with an improved pharmacokinetic profile compared to 1. Characterization of 15i in vivo in the fear-potentiated startle (FPS) paradigm revealed a robust reduction of conditioned fear behavior. This effect nicely correlates with the rat brain pharmacokinetics. |
doi_str_mv | 10.1021/ml100215b |
format | article |
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source | Open Access: PubMed Central; American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Letter |
title | Benzimidazoles as Potent and Orally Active mGlu5 Receptor Antagonists with an Improved PK Profile |
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