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Evaluates antioxidant and neuroprotective activity in pyrrole-based compounds, suggesting potential for neurodegenerative treatment.
Pyrrole-based hydrazide–hydrazones constitute a class of organic compounds that has attracted increasing attention in pharmaceutical research due to their potential application in the treatment of neurodegenerative diseases. In the present study, a series of ten novel pyrrole-containing hydrazide–hydrazones was synthesized. The structures of the newly obtained compounds were characterized by IR spectrophotometry, 1H-NMR, and 13C-NMR spectroscopy, while their purity was confirmed by mass spectrometry and melting point determination. The antioxidant activity of the synthesized compounds was evaluated in vitro using ABTS, DPPH, FRAP, and a commercial Antioxidant Assay Kit (CS0790). Their neurotoxicity and neuroprotective effects were subsequently assessed in rat brain subcellular fractions. Two of the tested compounds, VV4 and VV6, exhibited the most pronounced antioxidant and neuroprotective effects, along with the lowest levels of neurotoxicity. The key pharmacokinetic parameters of the most active compounds were predicted in silico, and their stability and reactivity were subsequently evaluated using DFT analysis.
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Karatchobanov et al. (2026) studied this question.
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