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DTC2162 is a novel, highly potent, and selective small-molecule inhibitor of 4R tau aggregation developed by the Korea Institute of Science and Technology (KIST). It is being investigated for the treatment of tauopathies, specifically progressive supranuclear palsy (PSP) and Alzheimer's disease (AD). DTC2162 acts as a reversible covalent inhibitor of disulfide-dependent tau oligomerization, thereby preventing the formation of toxic tau oligomers and protecting against neuronal cell death. In preclinical models of tauopathy (P301L Tau-BiFC transgenic mice), DTC2162 has demonstrated significant efficacy in reducing tau pathology and restoring cognitive and motor functions.
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