Oxazoline/amide derivatives against M. tuberculosis: experimental, biological and computational investigations

dc.contributor.authorBajpai, Priyanka
dc.contributor.authorSingh, Ankit Kumar
dc.contributor.authorKandagalla, Shivanada
dc.contributor.authorChandra, Phool
dc.contributor.authorKumar Sah, Vimlendu
dc.contributor.authorKumar, Pradeep
dc.contributor.authorGrishina, Maria
dc.contributor.authorVerma, Om Prakash
dc.contributor.authorPathak, Prateek
dc.date.accessioned2024-01-21T10:38:39Z
dc.date.accessioned2024-08-13T12:05:36Z
dc.date.available2024-01-21T10:38:39Z
dc.date.available2024-08-13T12:05:36Z
dc.date.issued2023-11-10T00:00:00
dc.description.abstractTuberculosis (TB) is a treatable contagious disease that continuously kills approximately 2 million people yearly. Different oxazoline/amide derivatives were synthesized, and their anti-tuberculosis activity was performed against different strains of Mtb. This study designed the anti-Mtb compounds based on amide and oxazoline, two different structural moieties. The compounds were further synthesized and characterized by spectral techniques. Their anti-Tb activity was evaluated against strain (M. tuberculosis: H37Rv). Selectivity and binding affinity of all synthesized compounds (2a�2e, 3a�3e) against PanK in Mtb were investigated through molecular docking. Molecular dynamics simulation studies for the promising compounds 2d and 3e were performed for 100 ns. The stability of these complexes was assessed by calculating the root mean square deviation, solvent-accessible surface area, and gyration radius relative to their parent structures. Additionally, free energy of binding calculations were performed. Among all synthesized compounds, 2d and 3e had comparable antitubercular activity against standard drug, validated by their computational and biological study. � 2023 Informa UK Limited, trading as Taylor & Francis Group.en_US
dc.identifier.doi10.1080/07391102.2023.2276312
dc.identifier.issn7391102
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/3626
dc.identifier.urlhttps://www.tandfonline.com/doi/full/10.1080/07391102.2023.2276312
dc.language.isoen_USen_US
dc.publisherTaylor and Francis Ltd.en_US
dc.subjectamideen_US
dc.subjectand simulationsen_US
dc.subjectH37Rven_US
dc.subjectM. tuberculosisen_US
dc.subjectmolecular dockingen_US
dc.subjectoxazolineen_US
dc.titleOxazoline/amide derivatives against M. tuberculosis: experimental, biological and computational investigationsen_US
dc.title.journalJournal of Biomolecular Structure and Dynamicsen_US
dc.typeArticleen_US
dc.type.accesstypeClosed Accessen_US

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