There is a consensus that epigenomic changes play a significant role in carcinogenesis.The effect of DNA methylation and its increased modulations on gene expression during carcinogenesis is significant for diagnostic and therapeutic purposes.Potential phytochems. as anticancer approach modulators of epigenetic pathways are the focus of this investigation.Mol. docking studies were conducted to foretell how phytochems. will interact with DNMT3A.As part of our effort to identify novel anti-cancer treatments, we examined a wide variety of phytochems. from many chem. classes, including cannabinoids, carotenoids, chalcones, fatty acids, lignans, polysaccharides, saponins, steroids, and tannins.The docking scores for Dihydromyricetin are -10.207 kcal/mol, -9.313 kcal/mol for S-Adenosyl-L-methionine (SAM), and -8.757 kcal/mol for Zeylenol were determined to be superior than to phytochem. inhibitors against DNMT3A in the virtual screening method.Docking scores, hydrogen bond interactions, ADME characteristics, and DFT.Mol. Dynamics Simulation and free energy calculations demonstrated that these compounds bind stably to DNMT3A, potentially inhibiting its activity.Network Pharmacol. suggested Dihydromyricetin′s specific anticancer potential against cervical cancer.These findings provide insights into protein-Ligand interactions with Dnmt3A and highlights the need for In-vitro validation.