Journal
JOURNAL OF MEDICINAL CHEMISTRY
Volume -, Issue -, Pages -Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jmedchem.2c00799
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Funding
- University Grants Commission (UGC) [2021-14513]
- Indian Council of Medical Research (ICMR) Adhoc Grant
- [30-564/2021]
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Huntington's disease is a neuro-degenerative disorder caused by a mutation in the huntingtin gene. New research has led to the discovery of small-molecule therapeutics that show promise for treating this disease. This article summarizes the development of these therapeutics, including their structure, therapeutic effects, and mechanisms of action. Additionally, the key drivers of Huntington's disease pathogenesis are highlighted to aid in the design of effective treatments.
Huntington's disease (HD) is a progressive neuro-degenerative disorder caused by a CAG repeat expansion in the huntingtin gene (HTT). The new insights into HD's cellular and molecular pathways have led to the identification of numerous potent small-molecule therapeutics for HD therapy. The field of HD-targeting small-molecule therapeutics is accelerating, and the approval of these therapeutics to combat HD may be expected in the near future. For instance, preclinical candidates such as naphthyridine-azaquinolone, AN1, AN2, CHDI-00484077, PRE084, EVP4593, and LOC14 have shown promise for further optimization to enter into HD clinical trials. This perspective aims to summarize the advent of small-molecule therapeutics at various stages of clinical development for HD therapy, emphasizing their structure and design, therapeutic effects, and specific mechanisms of action. Further, we have highlighted the key drivers involved in HD pathogenesis to provide insights into the basic principle for designing promising anti-HD therapeutic leads.
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