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Discovery of an Orally Bioavailable and Central Nervous System (CNS) Penetrant mGlu7 Negative Allosteric Modulator (NAM) in Vivo Tool Compound: N-(2-(1 H-1,2,4-triazol-1-yl)-5-(trifluoromethoxy)phenyl)-4-(cyclopropylmethoxy)-3-methoxybenzamide (VU6012962).


ABSTRACT: Herein, we report the discovery of a new, orally bioavailable and CNS-penetrant metabotropic glutamate receptor 7 (mGlu7) negative allosteric modulator (NAM) that achieves exposure in cerebral spinal fluid (CSF) 2.5× above the in vitro IC50 at minimum effective doses (MEDs) of 3 mg/kg in preclinical anxiety models.

SUBMITTER: Reed CW 

PROVIDER: S-EPMC6501583 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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Discovery of an Orally Bioavailable and Central Nervous System (CNS) Penetrant mGlu<sub>7</sub> Negative Allosteric Modulator (NAM) in Vivo Tool Compound: N-(2-(1 H-1,2,4-triazol-1-yl)-5-(trifluoromethoxy)phenyl)-4-(cyclopropylmethoxy)-3-methoxybenzamide (VU6012962).

Reed Carson W CW   Yohn Samantha E SE   Washecheck Jordan P JP   Roenfanz Hanna F HF   Quitalig Marc C MC   Luscombe Vincent B VB   Jenkins Matthew T MT   Rodriguez Alice L AL   Engers Darren W DW   Blobaum Anna L AL   Conn P Jeffrey PJ   Niswender Colleen M CM   Lindsley Craig W CW  

Journal of medicinal chemistry 20190117 3


Herein, we report the discovery of a new, orally bioavailable and CNS-penetrant metabotropic glutamate receptor 7 (mGlu<sub>7</sub>) negative allosteric modulator (NAM) that achieves exposure in cerebral spinal fluid (CSF) 2.5× above the in vitro IC<sub>50</sub> at minimum effective doses (MEDs) of 3 mg/kg in preclinical anxiety models. ...[more]

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