Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/3958
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dc.contributor.authorKumar, Nareshen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-17T15:31:09Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-17T15:31:09Z-
dc.date.issued2020-
dc.identifier.citationYadav, T. C., Kumar, N., Raj, U., Goel, N., Vardawaj, P. K., Prasad, R., & Pruthi, V. (2020). Exploration of interaction mechanism of tyrosol as a potent anti-inflammatory agent. Journal of Biomolecular Structure and Dynamics, 38(2), 382-397. doi:10.1080/07391102.2019.1575283en_US
dc.identifier.issn0739-1102-
dc.identifier.otherEID(2-s2.0-85063209457)-
dc.identifier.urihttps://doi.org/10.1080/07391102.2019.1575283-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/3958-
dc.description.abstractDrug discovery for a vigorous and feasible lead candidate is a challenging scientific mission as it requires expertise, experience, and huge investment. Natural products and their derivatives having structural diversity are renowned source of therapeutic agents since many years. Tyrosol (a natural phenylethanoid) has been extracted from olive oil, and its structure was confirmed by elemental analysis, FT-IR, FT-NMR, and single crystal X-ray crystallography. The conformational analysis for tyrosol geometry was performed by Gaussian 09 in terms of density functional theory. Validation of bond lengths and bond angles obtained experimentally as well as theoretically were performed with the help of curve fitting analysis, and values of correlation coefficient (R) obtained as 0.988 and 0.984, respectively. The charge transfer within the tyrosol molecule was confirmed by analysis of HOMO→LUMO molecular orbitals. In molecular docking with COX-2 (PDB ID: 5F1A), tyrosol was found to possess satisfactory binding affinity as compared to other NSAIDs (Aspirin, Ibuprofen, and Naproxen) and a COX-2 selective drug (Celecoxib). ADMET prediction, drug-likeness and bioactivity score altogether confirm the lead/drug like potential of tyrosol. Further investigation of simulation quality plot, RMSD and RMSF plots, ligands behavior plot as well as post simulation analysis manifest the consistency of 5F1A-tyrosol complex throughout the 20 ns molecular simulation process that signifies its compactness and stability within the receptor pocket. AbbreviationsADMET Absorption, Distribution, Metabolism, Excretion and ToxicityÅ AngstromCOX-2 Cyclooxygenase-2DFT Density Functional TheoryDMF DimethylformamideFMO Frontier Molecular OrbitalFT-IR Fourier-transform Infrared SpectroscopyFT-NMR Nuclear Magnetic Resonance SpectroscopyHOMO Highest Occupied Molecular OrbitalLUMO Lowest Unoccupied Molecular OrbitalMD Molecular DynamicsNS NanosecondNSAIDs Non-steroidal anti-inflammatory drugsOPE Osiris Property ExplorerRMSD Root-Mean-Square DeviationRMSF Root Sean Square Fluctuation Communicated by Ramaswamy H. Sarma. © 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.en_US
dc.language.isoenen_US
dc.publisherTaylor and Francis Ltd.en_US
dc.sourceJournal of Biomolecular Structure and Dynamicsen_US
dc.subjectacetylsalicylic aciden_US
dc.subjectcelecoxiben_US
dc.subjectcyclooxygenase 2en_US
dc.subjectibuprofenen_US
dc.subjectnaproxenen_US
dc.subjecttyrosolen_US
dc.subject4-hydroxyphenylethanolen_US
dc.subjectantiinflammatory agenten_US
dc.subjectliganden_US
dc.subjectphenethyl alcoholen_US
dc.subjectproteinen_US
dc.subjectanimal cellen_US
dc.subjectArticleen_US
dc.subjectbinding affinityen_US
dc.subjectbiological activityen_US
dc.subjectchemical bonden_US
dc.subjectcorrelation coefficienten_US
dc.subjectdensity functional theoryen_US
dc.subjectdrug conformationen_US
dc.subjectdrug receptor bindingen_US
dc.subjectdrug structureen_US
dc.subjectelemental analysisen_US
dc.subjectFourier transform infrared spectroscopyen_US
dc.subjectgeometryen_US
dc.subjecthumanen_US
dc.subjecthuman cellen_US
dc.subjectmolecular dockingen_US
dc.subjectmolecular dynamicsen_US
dc.subjectnonhumanen_US
dc.subjectnuclear magnetic resonanceen_US
dc.subjectpriority journalen_US
dc.subjectX ray crystallographyen_US
dc.subjectchemistryen_US
dc.subjectconformationen_US
dc.subjectinfrared spectroscopyen_US
dc.subjectnuclear magnetic resonance spectroscopyen_US
dc.subjectthermodynamicsen_US
dc.subjectAnti-Inflammatory Agentsen_US
dc.subjectCrystallography, X-Rayen_US
dc.subjectLigandsen_US
dc.subjectMagnetic Resonance Spectroscopyen_US
dc.subjectMolecular Conformationen_US
dc.subjectMolecular Docking Simulationen_US
dc.subjectMolecular Dynamics Simulationen_US
dc.subjectPhenylethyl Alcoholen_US
dc.subjectProteinsen_US
dc.subjectSpectroscopy, Fourier Transform Infrareden_US
dc.subjectThermodynamicsen_US
dc.titleExploration of interaction mechanism of tyrosol as a potent anti-inflammatory agenten_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Biosciences and Biomedical Engineering

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