Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/63902
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dc.contributor.authorBarukial, Pratyashee-
dc.contributor.authorAhmed, Benzir-
dc.contributor.authorSingha, Basanta-
dc.contributor.authorChetia, Pankaj-
dc.contributor.authorDas, Nipu Kumar-
dc.contributor.authorThakur, Samir-
dc.contributor.authorSinha, Upasana Bora-
dc.contributor.authorBezbaruah, Bipul-
dc.date.accessioned2024-05-16T06:20:30Z-
dc.date.available2024-05-16T06:20:30Z-
dc.date.issued2024-05-
dc.identifier.issn0975-0959 (Online); 0301-1208 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/63902-
dc.description354-370en_US
dc.description.abstractNon-covalent interactions have long been an emerging area of research in anticancer drug-DNA binding investigations since in vivo biomolecules are the primary target sites for all types of drug molecules. This study delves into the interaction of five promising Co(II)-Schiff base complexes (M1-M5) with DNA nucleobases, employing a multi-pronged approach to unveil their anticancer activity and interaction mechanisms. Density functional theory (DFT) provided a deep dive into the complexes' electronic structures, shedding light on how they interact with DNA nucleobases, their stability within these interactions, and the overall geometry involved. Further insights were gleaned from analysing frontier molecular orbitals (FMOs), molecular electrostatic potential (MEP), and non-covalent interactions (NCI) to investigate other important aspects of Co(II)-Schiff base complexes with the receptor AT/GC base pairs. Moreover, molecular docking simulations predicted the preferred binding sites and orientations of these complexes with B-DNA dodecamer, offering a realistic picture of their interactions with DNA in a larger context. Further, we also carried out Absorption, Distribution, Metabolism, Excretion, and Toxicity (ADMET) studies to analyse the pharmacokinetic and physicochemical properties of the Co(II)-Schiff base complexes. DFT study suggest that the Complex M1 exhibits a strong affinity for both AT and GC base pairs, as indicated by its high negative interaction energy values of -18.55 kcal/mol for AT and -23.42 kcal/mol for GC.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR,Indiaen_US
dc.sourceIJBB Vol.61(06) [June 2024]en_US
dc.subjectADMETen_US
dc.subjectAT/GCen_US
dc.subjectDNA nucleobasesen_US
dc.subjectNCIen_US
dc.subjectRDGen_US
dc.titleSome Co(II)-Schiff base complexes as promising anticancer agents: A DFT and molecular docking studyen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijbb.v61i6.8609en_US
Appears in Collections:IJBB Vol.61(06) [June 2024]

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