DN-1289 is an orally active and selective inhibitor of dual leucine zipper kinase ( DLK ; IC 50 =17 nM) and leucine zipper-bearing kinase ( LZK ; IC 50 =40 nM). DN-1289 results significant attenuation of optic nerve crush (ONC)-induced p-c-Jun in mice model. DN-1289 has excellent in vivo plasma half-life and blood-brain barrier permeability.
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