03274ntm a2200349 i 4500 MY-KuUP 20260421124755.0 t||||fr|||| 000 0 ta 260421t20252025my a|||fr|||| 000 0 eng d THE0010487 (Local) Hardback UMPSA eng UMPSA rda FIST .J53 2025 r Bc. Ong, Jia Xian, author. Synthesis and docking simulation of 2- benzoylcyclohexanon e for potential colon cancer treatment / Ong Jia Xian Kuantan, Pahang : UMPSA, 2025 © 2025 xiv, 72pages : illustrations ; rdacontent text rdamedia unmediated rdacarrier volume rda text file PDF Faculty of Industrial Sciences and Technology Final Year Report (Bachelor of Applied Science of Industrial Chemistry) -- Universiti Malaysia Pahang Al-Sultan Abdullah - 2025 Include bibliographical reference Colorectal cancer (CRC) remains one of the leading causes of cancer-related mortality globally, emphasizing the need for innovative therapeutic approaches. This study explores the synthesis, characterization, and molecular docking analysis of 2- benzyolcyclohexanone compound, focusing on 2-benzoylcyclohexanone as a promising potential inhibitor of the epidermal growth factor receptor (EGFR), a pivotal protein in CRC progression. The research was conducted in two phases: the first involved the synthesis of the 2-benzyolcyclohexanone compound using Stork enamine alkylation and nucleophilic substitution methods, followed by structural characterization using Fouriertransform infrared (FTIR) and nuclear magnetic resonance (NMR) spectroscopy. FTIR analysis revealed characteristic carbonyl peaks at 1710.51 cm⁻¹ and 1683.10 cm⁻¹, confirming the 2-benzyolcyclohexanone structure. The 1H proton NMR spectrum exhibited aromatic signals between 1.773 and 4.335 ppm, further validating the compound's structure. In the second phase, molecular docking simulations were performed using SwissDock to investigate binding interactions with EGFR. The synthesized 2-benzyolcyclohexanone demonstrated moderate binding affinity (binding energy: -4.824 kcal/mol) compared to Fruquintinib (-5.398 kcal/mol) and AQ4 (-4.895 kcal/mol). Key interactions included hydrophobic forces and π-stacking, which are critical for receptor inhibition. Despite a slightly lower binding affinity than standard inhibitors, 2-benzoylcyclohexanone exhibits significant potential as a lead compound due to its 2-benzyolcyclohexanone scaffold, which serves as an excellent starting point for further optimization.This study establishes a foundation for the development of accessible and cost-effective CRC treatments. Future directions include in vitro cytotoxicity assays, structure-activity relationship (SAR) studies, and in vivo testing to enhance the compound's efficacy and safety profile. Faculty of Industrial Sciences and Technology Dissertations Universities and colleges Dissertations Theses Dissertations https://umpir.ump.edu.my/id/eprint/46139 lcc PSM 0 0 lcc 0 0 10000 10000 2026-04-21 0 FIST .J53 2025 r Bc. T000003759 2026-04-21 12:48:18 2026-04-21 PSM 104765 104771