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Exploring the Hydrazone Group in Multifunctional Approaches for Alzheimer's Disease Therapy
Carola Grondona1, Eleonora Russo1, Bruno Tasso1
1Department of Pharmacy, University of Genoa, Genoa, Italy.
Hydrazone compounds show promise for Alzheimer's disease (AD) therapy by targeting multiple pathological pathways. This review highlights their potential to combat the complex, multifactorial nature of AD, offering new therapeutic avenues.
Area of Science:
- Medicinal Chemistry
- Neuroscience
- Pharmacology
Background:
- Alzheimer's disease (AD) is a complex neurodegenerative disorder with multiple pathological processes.
- Current single-target therapies offer limited symptomatic relief, necessitating novel approaches for disease modification.
- Hydrazones are versatile chemical scaffolds with potential for multitarget drug design.
Purpose of the Study:
- To provide a comprehensive overview of hydrazone-containing compounds for AD therapy.
- To highlight the activity of hydrazones against classical and emerging AD targets.
- To analyze structure-activity relationships and design strategies for hydrazone-based multitarget-directed ligands (MTDLs).
Main Methods:
- Literature review of hydrazone compounds reported between 2020-2025.
- Analysis of their activity on key enzymes and pathological mechanisms in AD.
- Evaluation of multitarget profiles and structure-activity relationships (SARs).
Main Results:
- Hydrazone-based MTDLs demonstrate efficacy against multiple AD-related targets, including cholinesterases (ChEs), carbonic anhydrase, BACE1, and α-glycosidase.
- These compounds exhibit potential for addressing the multifactorial nature of AD.
- Rational design strategies are being employed to optimize hydrazone scaffolds for AD treatment.
Conclusions:
- Hydrazone-based MTDLs represent a promising strategy for developing effective Alzheimer's disease therapies.
- Their ability to modulate multiple pathogenic pathways offers a significant advantage over single-target approaches.
- Further research into hydrazone chemistry holds potential for advancing AD treatment.
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