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GSK2578215A; a potent and highly selective 2-arylmethyloxy-5-substitutent-N-arylbenzamide LRRK2 kinase inhibitor.


ABSTRACT: Leucine-rich repeat kinase 2 (LRRK2) is a promising therapeutic target for some forms of Parkinson's disease. Here we report the discovery and characterization of 2-arylmethyloxy-5-subtitutent-N-arylbenzamides with potent LRRK2 activities exemplified by GSK2578215A which exhibits biochemical IC(50)s of around 10 nM against both wild-type LRRK2 and the G2019S mutant. GSK2578215A exhibits exceptionally high selectivity for LRRK2 across the kinome, substantially inhibits Ser910 and Ser935 phosphorylation of both wild-type LRRK2 and G2019S mutant at a concentration of 0.3-1.0 ?M in cells and in mouse spleen and kidney, but not in brain, following intraperitoneal injection of 100mg/kg.

SUBMITTER: Reith AD 

PROVIDER: S-EPMC4208292 | biostudies-literature | 2012 Sep

REPOSITORIES: biostudies-literature

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GSK2578215A; a potent and highly selective 2-arylmethyloxy-5-substitutent-N-arylbenzamide LRRK2 kinase inhibitor.

Reith Alastair D AD   Bamborough Paul P   Jandu Karamjit K   Andreotti Daniele D   Mensah Lucy L   Dossang Pamela P   Choi Hwan Geun HG   Deng Xianming X   Zhang Jinwei J   Alessi Dario R DR   Gray Nathanael S NS  

Bioorganic & medicinal chemistry letters 20120707 17


Leucine-rich repeat kinase 2 (LRRK2) is a promising therapeutic target for some forms of Parkinson's disease. Here we report the discovery and characterization of 2-arylmethyloxy-5-subtitutent-N-arylbenzamides with potent LRRK2 activities exemplified by GSK2578215A which exhibits biochemical IC(50)s of around 10 nM against both wild-type LRRK2 and the G2019S mutant. GSK2578215A exhibits exceptionally high selectivity for LRRK2 across the kinome, substantially inhibits Ser910 and Ser935 phosphory  ...[more]

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