GNE-8505 is an orally active, blood-brain barrier-permeable selective dual leucine zipper kinase ( DLK ) inhibitor. GNE-8505 has an IC 50 of 0.144 μM for pJNK , and EC 50 of 0.457 μM for DRG . GNE-8505 inhibits the DLK / JNK pathway, reduces stress-induced c-Jun phosphorylation levels, decreases neuronal death and suppresses axonal degeneration. GNE-8505 reduces phosphorylated c-Jun levels in the retina, spinal cord and brain tissues of mice. GNE-8505 is applicable to research related to Alzheimer's disease and amyotrophic lateral sclerosis (ALS).
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