Spectroscopic characterization and quantum chemical calculations on Favipiravir-Guanine biomolecular complex

Abstract

Favipiravir, a medication, has drawn a lot of interest recently as a possible therapeutic option for viral illnesses such as the COVID-19 pandemic. In the current work, Favipiravir + Guanine combination is being spectroscopically characterized using Fourier Transformed Infrared Spectroscopy, Raman, and Surface-Enhanced Raman Spectroscopy tools. Density functional theory along with the Becke 3-Parameter, Lee-Yang-Parr method and the basis set 6-311++ G(d,p) is used to explore the molecular interactions between the monomers of Guanine and Favipiravir. The stability of the complex resulting from the charge delocalization is thoroughly examined by natural bond orbital analysis that demonstrates the C=O∙∙∙H intermolecular hydrogen bond formation. The nature of the intermolecular hydrogen bond is described using atoms in molecules analysis. Molecular electrostatic potential mapping depicts various regions of electrostatic potential for the molecules, characterizing their reactive nature. The complex’s frontier molecular orbital gap of 2.39 eV indicates a higher possibility of electronic charge transfer, which in turn enhances the chemical reactivity of the complex. An analysis of the complex’s hyperpolarizability reveals a good non-linear optical response. The antiviral activity of the Favipiravir + Guanine complex is demonstrated by its molecular docking against the 6LU7 receptor (−5.61 kcal/mol).

Keywords:

• AIM
• Favipiravir + Guanine
• FTIR
• Raman
• molecular docking

Acknowledgments

The authors are grateful to FIST-DST, Delhi, for Raman instrumentation facilities in the Department of Physics, NERIST, Arunachal Pradesh, India. Authors are also thankful to the Department of Physics, Manipur University, for providing FTIR spectroscopy facilities.

Disclosure statement

No potential conflict of interest was reported by the author(s).