Exploration of 4-Chloro-3-nitrocoumarin: Spectroscopic Analysis, DFT Insights, Molecular Docking, Assessments of Antibacterial and In Vitro Anticancer Activities as a Potent Bioactive Agent

Authors

Abstract

The detailed theoretical and experimental (FT-IR, FT-Raman, UV-visible) spectroscopy analyses of the 4-Chloro-3-nitrocoumarin (CNC) molecule were carried out. The CNC compound's pharmacological properties were also investigated utilizing antibacterial and anticancer activity investigations. Initially, the CNC molecule was optimized by the density functional theory B3LYP method with a cc-pVTZ basis set using the Gaussian 09W program.   The optimized molecular structure provides the harmonic vibrational frequencies of the CNC molecule. The observed and computed vibrational wavenumbers were assigned and found to be well correlated.  UV-Vis absorption spectrum analysis indicates that the molecule contains π→π* electronic transition. Frontier molecular orbitals (FMOs) analysis indicates that the LUMO of CNC molecule is mainly located over the nitro group, it indicates that the nitro group is particularly prone to accepting electrons from other molecules and participate in chemical reactions where acts as an electrophile. Mulliken atomic charge distribution analysis further confirms the FMOs results. The antibacterial test results validate that the CNC molecule exhibits a stronger inhibitory effect on Staphylococcus aureus compared to the other tested bacteria.  In vitro anticancer cytotoxicity analysis clearly evidences that the CNC compound inhibits the growth of HeLa cervical cancer cell lines more than A549 lung cancer cell lines. In silico molecular docking study further validates that the CNC molecule inhibits the function of the p38a Mitogen-activated protein kinase 14, which has been associated with cervical cancer.  As a result, the present study paves the way for the development of new drugs to treat cervical cancer.

Keywords: 4-Chloro-3-nitrocoumarin; DFT; FT-IR; FT-Raman; Anticancer; Molecular docking; Cervical cancer drug.

Keywords:

4-Chloro-3-nitrocoumarin, DFT, FT-IR, FT-Raman, Anticancer, Molecular docking, Cervical cancer drug

DOI

https://doi.org/10.22270/jddt.v13i12.6165

Author Biographies

Surya S. Mohan, Research scholar (Reg.No.20213092132012), Department of Physics, Muslim Arts College, Thiruvithancode-629174, Affiliated to Manonmaniam Sundaranar University, Abishekapatti, Tirunelveli-627 012, Tamil Nadu, India.

Research scholar (Reg.No.20213092132012), Department of Physics, Muslim Arts College, Thiruvithancode-629174,  Affiliated to Manonmanium Sundaranar University, Abishekapatti, Tirunelveli-627 012, Tamil Nadu, India.

M.R. Meera, Department of Physics, Sree Ayyappa College for Women, Chunkankadai, Nagercoil-629 003, Tamil Nadu, India.

Department of Physics, Sree Ayyappa College for Women, Chunkankadai, Nagercoil-629 003, Tamil Nadu, India.

A. Rathika, Department of Physics, Muslim Arts College, Thiruvithancode-629174, Tamil Nadu, India.

Department of Physics, Muslim Arts College, Thiruvithancode-629174, Tamil Nadu, India.

R. Premkumar, Department of Physics, N.M.S.S.V.N. College, Madurai-625019, Tamil Nadu, India.

Department of Physics, N.M.S.S.V.N. College, Madurai-625019, Tamil Nadu, India.

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Published

2023-12-15
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How to Cite

1.
Mohan SS, Meera M, Rathika A, Premkumar R. Exploration of 4-Chloro-3-nitrocoumarin: Spectroscopic Analysis, DFT Insights, Molecular Docking, Assessments of Antibacterial and In Vitro Anticancer Activities as a Potent Bioactive Agent. J. Drug Delivery Ther. [Internet]. 2023 Dec. 15 [cited 2026 May 26];13(12):189-200. Available from: https://jddtonline.info/index.php/jddt/article/view/6165

How to Cite

1.
Mohan SS, Meera M, Rathika A, Premkumar R. Exploration of 4-Chloro-3-nitrocoumarin: Spectroscopic Analysis, DFT Insights, Molecular Docking, Assessments of Antibacterial and In Vitro Anticancer Activities as a Potent Bioactive Agent. J. Drug Delivery Ther. [Internet]. 2023 Dec. 15 [cited 2026 May 26];13(12):189-200. Available from: https://jddtonline.info/index.php/jddt/article/view/6165