LRRK2
渗透剂(生化)
激酶
化学
磷酸化
药理学
生物化学
生物
突变
有机化学
基因
作者
Albert W. Garofalo,Jacob B. Schwarz,Kerry Zobel,Claudia Beato,Silvia Bernardi,Federica Budassi,Laura Caberlotto,Peng Gao,Cristiana Griffante,Xinying Liu,Marco Migliore,Feifei Qiao,Fabio Maria Sabbatini,Anna Sava,Mingliang Zhang,Holly J. Carlisle
标识
DOI:10.1016/j.bmcl.2023.129487
摘要
The G2019S variant of LRRK2, which causes an increase in kinase activity, is associated with the occurrence of Parkinson's disease (PD). Potent, mutation-selective, and brain penetrant inhibitors of LRRK2 can suppress the biological effects specific to G2019S LRRK2 that cause pathogenicity. We report the discovery of a series of cyanoindane and cyanotetralin kinase inhibitors culminating in compound 34 that demonstrated selective inhibition of phosphorylation of LRRK2 in the mouse brain. These novel inhibitors may further enable the precision medicine path for future PD therapeutics.
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