The purpose of this work is to compare the hepatoprotective role of six active Phytochemicals of Bael—Marmelide, Marmenol, scoparone, 6,7-epoxyaurapetene, and Querectin catechin—as ligands. Techniques: using molecular docking to ascertain how a ligand interacts with its receptor. A lower docking score denotes a more stable protein binding. Findings: Through reacting with residues of amino acids HIS A64, Arg A56, GLY A66, ,ASN A136and HISA61 of the 1NFK receptor, marmelide, marmenol, scoparone, scopoletin, 6,7-epoxyaurapetene, and querectin catechin were found to have the potential to evolve as a heaptoprotective drug. Conclusions: HIS A64, Arg A56, GLY A66, ,ASN A136and HISA61 were amino acid residues implicated in ligand protein interactions according to molecular docking. ;