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Computational screening, synthesis and neuroprotective evaluation of small molecule for the treatment of alzheimer's disease
by
Pajaro-Castro, Nerlis
in
Alzheimer's disease
/ Beta secretase
/ cyclin-dependent kinase 5
/ Cytotoxicity
/ drug-like
/ gamma secretase
/ Medical treatment
/ neurodegenerative
/ Peptides
2024
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Computational screening, synthesis and neuroprotective evaluation of small molecule for the treatment of alzheimer's disease
by
Pajaro-Castro, Nerlis
in
Alzheimer's disease
/ Beta secretase
/ cyclin-dependent kinase 5
/ Cytotoxicity
/ drug-like
/ gamma secretase
/ Medical treatment
/ neurodegenerative
/ Peptides
2024
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Do you wish to request the book?
Computational screening, synthesis and neuroprotective evaluation of small molecule for the treatment of alzheimer's disease
by
Pajaro-Castro, Nerlis
in
Alzheimer's disease
/ Beta secretase
/ cyclin-dependent kinase 5
/ Cytotoxicity
/ drug-like
/ gamma secretase
/ Medical treatment
/ neurodegenerative
/ Peptides
2024
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Computational screening, synthesis and neuroprotective evaluation of small molecule for the treatment of alzheimer's disease
Journal Article
Computational screening, synthesis and neuroprotective evaluation of small molecule for the treatment of alzheimer's disease
2024
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Overview
BACKGROUND: Current treatments for Alzheimer’s disease primarily address symptoms, as no definitive therapeutic targets have been identified. OBJECTIVES: This study aims to conduct a virtual screening of small molecules and synthesize and evaluate one of the most promising candidates for Alzheimer’s therapy. METHODS: Using AutoDock Vina, compounds with drug-like properties were docked against key proteins implicated in Alzheimer's pathology: β-Secretase, γ-Secretase, Pin1, and Cdk5. The molecule with the highest in silico affinity (PubChem ID: 84378305) was synthesized and evaluated experimentally. Cytotoxicity and neuroprotective effects were assessed using the MTT assay in the presence of the Aβ25-35 peptide. RESULTS: Four candidate molecules showed strong binding affinity, ranging from -6.8 to -9.1 kcal/mol. The results showed that when SK-N-SH cells were simultaneously treated with Aß25-35 peptide (5 µM) and compound 84378305 (0,1 µM), the molecule exhibited significant neuroprotection (33%) after the 48 h of incubation. CONCLUSION: Findings indicate that this lead compound exhibits potential neuroprotective activity, highlighting its promise as a candidate for further development in Alzheimer’s disease treatment.
Publisher
Universidad de Antioquía,Universidad de Antioquia
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