FT-IR, UV–visible, and NMR Spectral Analyses, Molecular Structure, and Properties of Nevadensin Revealed by Density Functional Theory and Molecular Docking

ABSTRACT

Nevadensin 2-(4-methoxyphenyl)-5,7-dihydroxy-6,8-dimethoxy-4H-1-benzo-pyran-4-one] is a natural bioactive flavonoid compound that has the potential to become a novel “natural lead” in the field of drug discovery program. The molecular structure, vibrational frequencies, and corresponding vibrational assignment of nevadensin have been investigated experimentally and theoretically by employing the B3PW91/6–311++G(d,p) method. The fundamental vibrational wave numbers as well as their intensities were calculated, and a good correlation between experimental and scaled calculated wave numbers had been accomplished. The ultraviolet spectrum of the studied molecule was recorded in the region 200–500 nm, and the electronic properties were predicted by the time-dependent density functional theory approach. ¹H and ¹³C NMR spectra have been calculated by employing the gauge-independent atomic orbital method. Nevadensin has been reported to exhibit antimicrobial activities against both Gram-positive and Gram-negative bacteria and also against the fungal pathogens, highlighting the pharmacological importance of the molecule.

KEYWORDS:

• Density functional theory
• molecular docking
• nevadensin
• spectral analysis
• UV–vis analysis

Additional information

Funding

A.K.S. acknowledges the Council of Scientific & Industrial Research (CSIR), New Delhi for providing research fellowship (Grant No. 09/107(0359)/2012-EMR-I), and G.B. is thankful to the Department of Science & Technology (DST), New Delhi for providing financial support (Grant No. EMR/2014/001220).