| Literature DB >> 26531152 |
John M Ellard1, Andrew Madin1, Oliver Philps1, Mark Hopkin1, Scott Henderson1, Louise Birch1, Desmond O'Connor2, Tohru Arai3, Kazuma Takase4, Louise Morgan5, David Reynolds5, Sonia Talma5, Eimear Howley5, Ben Powney5, Andrew H Payne1, Adrian Hall1, Jane E Gartlon5, Lee A Dawson5, Luis Castro1, Peter J Atkinson6.
Abstract
Herein we describe a series of tetrahydrobenzotriazoles as novel, potent metabotropic glutamate receptor subtype 5 (mGlu5) positive allosteric modulators (PAMs). Exploration of the SAR surrounding the tetrahydrobenzotriazole core ultimately led to the identification of 29 as a potent mGlu5 PAM with a low maximal glutamate potency fold shift, acceptable in vitro DMPK parameters and in vivo PK profile and efficacy in the rat novel object recognition (NOR) assay. As a result 29 was identified as a suitable compound for progression to in vivo safety evaluation.Entities:
Keywords: Cognition; Metabotropic glutamate receptor 5 (mGlu5); Positive allosteric modulator (PAM); Tetrahydrobenzotriazole
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Year: 2015 PMID: 26531152 DOI: 10.1016/j.bmcl.2015.10.050
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823