Synthesis, structure determination, molecular interaction analysis, molecular docking studies, and anticancer activity investigation of a chalcone derivative: (2E)-2-[(2,4-dimethoxyphenyl)methylidene]-3,4 dihydronaphthalen-1(2H)-one

A new chalcone derivative was synthesized using Claisen-Schmidt condensation reaction and its struc-ture was determined using single-crystal X-Ray Diffraction (XRD) technique. Hirshfeld surfaces were gen-erated to visualize and quantify short contacts, regions of varying potentials, and C-H...p and p...p stacking interactions. 2D fingerprint plots were analyzed, in which the contribution due to H...H contact to the total Hirshfeld surface was found to be the most significant with 54.1%. The cytotoxicity assay proved that the compound is non-toxic to the normal Vero cell line. The anticancer activity studies affirm the potentiality of the compound to inhibit the growth of MCF-7 cell lines with 52.46% of cell viability at IC50 value of 7.8 lg/mL. Molecular docking simulation revealed that the ligand fits well at the active site of the target protein 1M17. In-silico pharmacokinetic studies reveal that the compound is orally active and demonstrates a good pharmacokinetic profile. Copyright (C) 2022 Elsevier Ltd. All rights reserved.Selection and peer-review under responsibility of the scientific committee of the XII th Biennial National Conference of Physics Academy of North East (PANE 2021).