4.6 Article

Nipecotic Acid Derivatives as Potent Agents against Neurodegeneration: A Preliminary Study

Journal

MOLECULES
Volume 27, Issue 20, Pages -

Publisher

MDPI
DOI: 10.3390/molecules27206984

Keywords

Alzheimer's Disease; multi-targeting compounds; nipecotic acid; oxidative stress; inflammation; acetylcholinesterase inhibitors

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Alzheimer's Disease is a neurodegenerative disorder characterized by memory loss and cognitive impairment. Current treatment options only alleviate symptoms, and effective treatments have not been obtained yet. In this study, a series of compounds with significant antioxidant and/or anti-inflammatory activity were identified, which could potentially be developed as multi-targeting agents against Alzheimer's Disease.
Alzheimer's Disease (AD) is a common neurodegenerative disorder characterized by memory loss and cognitive impairment. Its pathology has not been fully clarified and therefore highly effective treatments have not been obtained yet. Almost all the current treatment options aim to alleviate only the symptoms and not to eliminate the disease itself. Acetylcholinesterase inhibitors are the main therapeutic agents against AD, whereas oxidative stress and inflammation have been found to be of great significance for the development and progression of neurodegeneration. In this work, ethyl nipecotate (ethyl-piperidine-3-carboxylate), a heterocyclic carboxylic acid derivative, which acts as a GABA reuptake inhibitor and has been used in research for diseases involving GABAergic neurotransmission dysfunction, was amidated with various carboxylic acids bearing antioxidant and/or anti-inflammatory properties (e.g., ferulic acid, sinapic acid, butylated hydroxycinnamic acid). Most of our compounds have significant antioxidant potency as lipid peroxidation inhibitors (IC50 as low as 20 mu M), as oxidative protein glycation inhibitors (inhibition up to 57%), and act as DPPH reducing agents. Moreover, our compounds are moderate LOX inhibitors (up to 33% at 100 mu M) and could reduce rat paw edema induced by carrageenan by up to 61%. Finally, some of them possessed inhibitory activity against acetylcholinesterase (IC50 as low as to 47 mu M). Our results indicate that our compounds could have the potentiality for further optimization as multi-targeting agents directed against AD.

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