Structural elucidation, solvent (polar and non-polar) effect on electronic characterization, non-covalent charge interaction nature, topology and pharmacological studies on NLO active -argininium methanesufonate

Kanagathara, N.; Thirunavukkarasu, M.; Selvaraj, S.; Kumar, A. Ram; Marchewka, M.K.; Janczak, Jan

doi:10.1016/j.molliq.2023.122315

Cited by 10 publications

(1 citation statement)

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“…The symmetric and asymmetric stretching vibrations of methyl groups are typically observed between 2870 and 2980 cm −1 . 34,35 Theoretically, the CH 3 symmetric stretching occurs at 2922, 2899, 2892, 2891, and 2883 cm −1 , and experimentally, the corresponding mode is found in the FT-Raman spectrum at 2913 cm −1 . Similarly, the asymmetric stretching occurs at 2999, 2994, and 2972 cm −1 , and the corresponding experimental values are found at 3326 and 2967 cm −1 in the FT-IR spectrum.…”

Section: Vibrationsmentioning

confidence: 96%

Spectroscopic, Biological, and Topological Insights on Lemonol as a Potential Anticancer Agent

et al. 2023

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A monoterpene alcohol known as lemonol was investigated experimentally as well as theoretically in order to gain insights into its geometrical structure, vibrational frequencies, solvent effects on electronic properties, molecular electrostatic potential, Mulliken atomic charge distribution, natural bond orbital, and Nonlinear Optical properties. The frontier molecular orbital energy gap values of 5.9084 eV (gas), 5.9261 eV (ethanol), 5.9185 eV (chloroform), 5.9253 eV (acetone), and 5.9176 eV (diethyl ether) were predicted, and it shows the kinetic stability and chemical reactivity of lemonol. Topological studies were conducted using Multiwfn software to understand the binding sites and weak interactions in lemonol. The antiproliferative effect of lemonol against the breast cancer cell line Michigan Cancer Foundation (MCF-7) was determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, while nuclear damage, condensation, and reactive oxygen species generation were identified using acridine orange/ethidium bromide, propidium iodide, and dichlorodihydrofluorescein diacetate staining. The theoretical and experimental findings are highly correlated, confirming the structure, and the results of in vitro studies suggest that lemonol acts as a potent inhibitor against the human breast cancer cell line MCF-7, highlighting its strong antiproliferative activity.

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Section: Vibrationsmentioning

confidence: 96%