GNE-9605 is a highly potent, selective, and brain-penetrant LRRK2 inhibitor with IC50 of 19 nM.
IC50 value:
Target: LRRK2
GNE-9605 retained excellent predicted human metabolic stability when assayed in human liver microsomes and hepatocytes. In
addition, no reversible or time-dependent inhibition of any of the major CYP isoforms was observed. The demonstrated metabolic stability, brain penetration across multiple species, and selectivity of these inhibitors support their use in preclinical efficacy and safety studies.
分子式
C17H20N7OF4Cl
分子量
449.83
CAS号
1536200-31-3
运输条件
Room temperature in continental US; may vary elsewhere.