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Investigating the potential of 6-substituted 3-formyl chromone derivatives as anti-diabetic agents using in silico methods. | LitMetric

AI Article Synopsis

Article Abstract

In exploring nature's potential in addressing diabetes-related conditions, this study investigates the therapeutic capabilities of 3-formyl chromone derivatives. Utilizing in silico methodologies, we focus on 6-substituted 3-formyl chromone derivatives (1-16) to assess their therapeutic potential in treating diabetes. The research examined the formyl group at the chromone's C-3 position. ADMET, biological activities, were conducted along with B3LYP calculations using 3 different basis sets. The analogues were analyzed based on their parent structure obtained from PubChem. The HOMO-LUMO gap confirmed the bioactive nature of the derivatives, NBO analysis was performed to understand the charge transfer. PASS prediction revealed that 3-formyl chromone derivatives are potent aldehyde oxidase inhibitors, insulin inhibitors, HIF1A expression inhibitors, and histidine kinase. Molecular docking studies indicated that the compounds had a strong binding affinity with proteins, including CAD, BHK, IDE, HIF-α, p53, COX, and Mpro of SARS-CoV2. 6-isopropyl-3-formyl chromone (4) displayed the highest affinity for IDE, with a binding energy of - 8.5 kcal mol. This result outperformed the affinity of the reference standard dapagliflozin (- 7.9 kcal mol) as well as two other compounds that target human IDE, namely vitexin (- 8.3 kcal mol) and myricetin (- 8.4 kcal mol). MD simulations were revealed RMSD value between 0.2 and 0.5 nm, indicating the strength of the protein-ligand complex at the active site.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11162442PMC
http://dx.doi.org/10.1038/s41598-024-63237-yDOI Listing

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