Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/3958
Title: Exploration of interaction mechanism of tyrosol as a potent anti-inflammatory agent
Authors: Kumar, Naresh
Keywords: acetylsalicylic acid;celecoxib;cyclooxygenase 2;ibuprofen;naproxen;tyrosol;4-hydroxyphenylethanol;antiinflammatory agent;ligand;phenethyl alcohol;protein;animal cell;Article;binding affinity;biological activity;chemical bond;correlation coefficient;density functional theory;drug conformation;drug receptor binding;drug structure;elemental analysis;Fourier transform infrared spectroscopy;geometry;human;human cell;molecular docking;molecular dynamics;nonhuman;nuclear magnetic resonance;priority journal;X ray crystallography;chemistry;conformation;infrared spectroscopy;nuclear magnetic resonance spectroscopy;thermodynamics;Anti-Inflammatory Agents;Crystallography, X-Ray;Ligands;Magnetic Resonance Spectroscopy;Molecular Conformation;Molecular Docking Simulation;Molecular Dynamics Simulation;Phenylethyl Alcohol;Proteins;Spectroscopy, Fourier Transform Infrared;Thermodynamics
Issue Date: 2020
Publisher: Taylor and Francis Ltd.
Citation: Yadav, 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:10.1080/07391102.2019.1575283
Abstract: Drug 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.
URI: https://doi.org/10.1080/07391102.2019.1575283
https://dspace.iiti.ac.in/handle/123456789/3958
ISSN: 0739-1102
Type of Material: Journal Article
Appears in Collections:Department of Biosciences and Biomedical Engineering

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