Vibrational spectra, molecular level solvent interaction, stabilization, donor- acceptor energies, thermodynamic, non-covalent interaction and electronic behaviors of 6-Methoxyisoquinoline- anti tubercular agent

Abstract

The present research is a theoretical examination of 6-methoxyisoquinoline implementing Density Functional Theory quantum mechanical approach. Structural optimization was performed to achieve a stable molecular structure with the least amount of energy. Several protic and aprotic solvent interactions were performed using the IEF polarization continuum model to examine the reactivity and stability of the molecules. Molecular interactions with solvents were investigated using UV–Visible, HOMO-LUMO, MEP, NBO, and NLO properties, which shows some changes in the compound activity at solvent phases against gas phase. The molecular interaction of π*C1–N2 to π*C5 - C10 shows the higher stabilizing energy. DMSO solvent exhibits a very low band gap energy, favors the molecule's high stability. Molecular reactivity, interactions, and optical behavior were all readily apparent. The chemical reactivity of the compound was found good in water. The percentage of PED contributions was evaluated for each mode of vibrations using vibrational spectral investigation. Topological surface analysis was used for better understanding of molecular electron density, reactive center, and steric effect. ELF, LOL, and RDG was generated for compounds with different solvents. The distance of transition and the overlapping of electron and hole were calculated using electron hole analysis. Pharmacological assessments include drug likeness, ADME, toxicity, and a pre-ADMET online tool, which supports the biological capability of the compound. Finally, molecular docking with anti-tubercular protein was performed, and a Ramachandran plot of chosen protein was shown to explore stability.