Structural, Spectroscopic, and Molecular Docking Analysis of Benzophenone N(4)-methyl-N(4)-phenyl Thiosemicarbazone Using Density Functional Theory

Abstract

A new thiosemicarbazone derivative, benzophenone N(4)-methyl-N(4)-phenyl thiosemicarbazone (BMPT) is synthesized using benzophenone and N(4)-methyl-N(4)- phenylthiosemicarbazide as precursors. Synthesized ligand is characterized by Fourier Transform Infrared spectra (FTIR) and FT-Raman spectra. Complete quantitative assignments of vibrational modes are presented in terms of potential energy distribution (PED) using quantum chemical calculations using the density functional theory (DFT) approach. Natural bond orbital (NBO) and molecular electrostatic potential (MEP) surface analysis are used to estimate the correlation between molecular structure and biological activity at the electronic level. Hirshfeld surface analysis is used to interpret the intermolecular interactions and also to provide information about the percentage contribution of various intermolecular contacts in the crystal structure. Besides the above, molecular docking studies of BMPT ligand with 3RGF and 3EWD proteins are also performed to confirm the ability of BMPT ligand as an active pharmaceutical ingredient (API) of potential anticancer and antimalarial drugs.

Keywords:

• Thiosemicarbazone
• density functional theory
• natural bond orbital (NBO)
• Hirshfeld surface analysis
• molecular docking

Acknowledgments

One of the authors Varsha Rani would like to acknowledge the financial support as University Scholarship provided by Chaudhary Charan Singh University, Meerut, during this work.

Disclosure statement

No potential conflict of interest was reported by the authors.