dc.creatorHozhabr Araghi, Samira
dc.creatorAmalraj, John
dc.creatorSadeghi Googheri, Motahare
dc.creatorPyarasani, Radha D.
dc.creatorMohammad Sadegh, Mohammad Sadegh
dc.date2023-01-16T19:26:30Z
dc.date2023-01-16T19:26:30Z
dc.date2023
dc.date.accessioned2024-05-02T20:30:23Z
dc.date.available2024-05-02T20:30:23Z
dc.identifierhttp://repositorio.ucm.cl/handle/ucm/4377
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/9274622
dc.descriptionIn order to gain a molecular understanding of why quercetin characteristics are altered by glucosylation, DFT calculations and MD simulations were utilized. According to DFT findings, glucosylation of quercetin altered its structural stability, molecular polarity, molecular polarizability, and Gibbs free energy of transfer, which gives a molecular explanation for the observed alterations in the aqueous solubility and lipophilicity of derivatives. The outcomes of MD simulations also demonstrated how the various hydroxyl groups of quercetin interact with solvent molecules and how glucosylation can have an impact on that. Additionally, it was shown that glucosylation often increased the number of hydrogen bonds and the nonbonded interaction energies between the molecules of the solvent and the solute. The solubility behavior of glucosylated derivatives in water and alcoholic solvents can be reasonably interpreted molecularly using these results, which could suggest approaches for improving the features of these kinds of bioactive compounds.
dc.languageen
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.sourceComputational and Theoretical Chemistry, 1220, 113981
dc.subjectFlavonoid glycosides
dc.subjectSolubility
dc.subjectLipophilicity
dc.subjectRDF analysis
dc.subjectNonbonded interactions
dc.titleAn in-silico study to gain a comprehensive understanding of the effects of glucosylation on quercetin properties
dc.typeArticle


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