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• W3022863485 endingPage "2071" @default.
• W3022863485 startingPage "2071" @default.
• W3022863485 abstract "Alzheimer’s disease (AD) is the most common type of dementia and usually manifests as diminished episodic memory and cognitive functions. Caspases are crucial mediators of neuronal death in a number of neurodegenerative diseases, and caspase 8 is considered a major therapeutic target in the context of AD. In the present study, we performed a virtual screening of 200 natural compounds by molecular docking with respect to their abilities to bind with caspase 8. Among them, rutaecarpine was found to have the highest (negative) binding energy (−6.5 kcal/mol) and was further subjected to molecular dynamics (MD) simulation analysis. Caspase 8 was determined to interact with rutaecarpine through five amino acid residues, specifically Thr337, Lys353, Val354, Phe355, and Phe356, and two hydrogen bonds (ligand: H35-A: LYS353:O and A:PHE355: N-ligand: N5). Furthermore, a 50 ns MD simulation was conducted to optimize the interaction, to predict complex flexibility, and to investigate the stability of the caspase 8–rutaecarpine complex, which appeared to be quite stable. The obtained results propose that rutaecarpine could be a lead compound that bears remarkable anti-Alzheimer’s potential against caspase 8." @default.
• W3022863485 created "2020-05-13" @default.
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• W3022863485 date "2020-04-29" @default.
• W3022863485 modified "2023-10-13" @default.
• W3022863485 title "Study of Caspase 8 Inhibition for the Management of Alzheimer’s Disease: A Molecular Docking and Dynamics Simulation" @default.
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• W3022863485 doi "https://doi.org/10.3390/molecules25092071" @default.
• W3022863485 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7249184" @default.
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• W3022863485 hasPublicationYear "2020" @default.
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