Abstract

Docking results suggest that Amentoflavone has a higher affinity for investigated serine/threonine-protein kinases, indicating potential interactions that may influence the activities of these kinases. The negative values of the binding energies signify strong and stable interactions, suggesting that Amentoflavone could be a key molecule in modulating the functions of these kinases, which play crucial roles in cellular processes such as cell cycle regulation and apoptosis.

Keywords: Serine/threonine protein kinase, Amentoflavone, Molecular docking, Apoptosis