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DLK inhibitor (Belfer Neurodegeneration Consortium)

Development stage
Preclinical
Lead developer
Neurodegeneration Consortium
Modality
Small Molecules
Administration
Oral
01

Overview

This dual leucine zipper kinase (DLK) inhibitor is a small-molecule therapeutic candidate developed by the Belfer Neurodegeneration Consortium at MD Anderson Cancer Center. DLK is a key regulator of the neuronal stress response; its activation leads to axonal degeneration and neuronal apoptosis in various neurodegenerative conditions. By inhibiting DLK, this compound aims to preserve neuronal integrity and prevent the cognitive and sensory deficits associated with neurodegeneration. The program is currently in preclinical development, targeting a range of conditions including Alzheimer's disease, chemotherapy-induced peripheral neuropathy (CIPN), and chemotherapy-related cognitive impairment, commonly referred to as chemobrain.

Other names
dual leucine zipper kinase inhibitorDLK inhibitor
02

Targets

NTRK1 (Tropomyosin-related receptor kinase A)MAP3K12 (Mitogen-activated protein kinase kinase kinase 12)MAP3K13 (Mitogen-activated protein kinase kinase kinase 13)MEK5 (Mitogen-Activated Protein Kinase Kinase 5)

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