Alzheimer's disease (AD) is a progressive neurodegenerative brain disease. Thus, drugs including donepezil, rivastigmine, and galantamine are not entirely effective in the treatment of this multifactorial disease. The present study evaluates eight derivatives (3a-3h) as candidates with stronger anti-AD potential but with less side effects. Reactive oxygen species (ROS) assays were used to assess oxidative stress which involve in the neurodegeneration. The neuroprotective properties of 3e against oxidative stress were done in three experiments using MTT test. The anti-AD potential was determined based on their anticholinesterase inhibition ability, determined using Ellman's method, Abeta aggregation potential according to thioflavin (Th) fluorescence assay, and their antioxidative and anti-inflammatory activities. Compound 3e exhibited moderate cholinesterase inhibition activity (AChE, IC(50) = 0.131 microM; BuChE, IC(50) = 0.116 microM; SI = 1.13), significant inhibition of Abeta(1-42) aggregation (55.7%, at 5 microM) and acceptable neuroprotective activity. Extensive analysis of insvitro and insvivo assays indicates that new cyclopentaquinoline derivatives offer promise as candidates for new anti-AD drugs.
        
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Czarnecka K, Girek M, Krecisz P, Skibinski R, Latka K, Jonczyk J, Bajda M, Szymczyk P, Galita G, Kabzinski J, Majsterek I, Espargaro A, Sabate R, Szymanski P (2023) New cyclopentaquinoline and 3,5-dichlorobenzoic acid hybrids with neuroprotection against oxidative stress for the treatment of Alzheimer's disease J Enzyme Inhib Med Chem38: 2158822
Czarnecka K, Girek M, Krecisz P, Skibinski R, Latka K, Jonczyk J, Bajda M, Szymczyk P, Galita G, Kabzinski J, Majsterek I, Espargaro A, Sabate R, Szymanski P (2023) J Enzyme Inhib Med Chem38: 2158822