Discovery of multitargeting single agents as a novel route to the potential treatment of neurodegenerative diseases

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Authors: Jeetal Vyas, Anuj S. Jamenis, Krishna Kaku, Yesha V. Shah, Kristin M. Miner, Tarun N. Bhatia, Roxanne E. Kim, Ruoli Bai, Ernest Hamel, Rehana Khan Leak, Aleem Gangjee
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References: 72

Abstract

There are no cures for neurodegenerative diseases. The biggest hurdle to treating these disorders is that their clinical manifestation is rooted in multiple physiological processes. Therefore, efficacious pharmaceutical options will likely require two or more agents with different mechanisms of action. However, drug combinations have significant drawbacks, including overlapping toxicities and unique pharmacokinetic properties, particularly the rate and extent of central nervous system (CNS) penetration. A single agent with multiple mechanisms of action could overcome these drawbacks. We have recently discovered first-in-class novel single agents (compounds 1 and 2) that mildly inhibit clinically important kinases and subtly favor microtubule stability at concentrations that show no evidence of neuronal toxicity in primary neurons, while maintaining their ability to penetrate the CNS in vivo. It is important to note that the effects of these analogs are mild and are predicated on avoiding neurotoxicity. These multitargeting single agents provide a new structural modality with the potential to influence treatments for Parkinson's and Alzheimer's disease and serve as lead compounds for further optimization.

Fields of Study & Subjects

Microtubule and mitosis dynamics Pharmacological Receptor Mechanisms and Effects Parkinson's Disease Mechanisms and Treatments

Publication details

Journal / source
Bioorganic & Medicinal Chemistry Letters
Volume
133
Pages
130536–130536
Publication date
7 January 2026
Language
EN