| Literature DB >> 27075300 |
Darren W Engers, Anna L Blobaum, Rocco D Gogliotti, Yiu-Yin Cheung, James M Salovich, Pedro M Garcia-Barrantes, J Scott Daniels, Ryan Morrison, Carrie K Jones, Matthew G Soars1, Xiaoliang Zhuo1, Jeremy Hurley1, John E Macor1, Joanne J Bronson1, P Jeffrey Conn, Craig W Lindsley, Colleen M Niswender, Corey R Hopkins.
Abstract
The efficacy of positive allosteric modulators (PAMs) of the metabotropic glutamate receptor 4 (mGlu4) in preclinical rodent models of Parkinson's disease has been established by a number of groups. Here, we report an advanced preclinically characterized mGlu4 PAM, N-(3-chloro-4-fluorophenyl)-1H-pyrazolo[4,3-b]pyridin-3-amine (VU0418506). We detail the discovery of VU0418506 starting from a common picolinamide core scaffold and evaluation of a number of amide bioisosteres leading to the novel pyrazolo[4,3-b]pyridine head group. VU0418506 has been characterized as a potent and selective mGlu4 PAM with suitable in vivo pharmacokinetic properties in three preclinical safety species.Entities:
Keywords: CYP induction; Metabotropic glutamate receptor 4; Parkinson’s disease; mGlu4; pyrazolo[4,3-b]pyridine
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Year: 2016 PMID: 27075300 PMCID: PMC5031509 DOI: 10.1021/acschemneuro.6b00035
Source DB: PubMed Journal: ACS Chem Neurosci ISSN: 1948-7193 Impact factor: 4.418