Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/66044
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dc.contributor.authorKou, Jun-Feng-
dc.date.accessioned2025-07-06T16:28:58Z-
dc.date.available2025-07-06T16:28:58Z-
dc.date.issued2025-06-
dc.identifier.issn2583-1321 (Online);0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/66044-
dc.description557-570en_US
dc.description.abstractTwo ruthenium (II) complexes [Ru(tpy)(adtpy)]2+ (1) and [Ru(dtp)(adtpy)]2+ (2) have been synthesized and characterized. The DNA-binding behavior of complexes have been studied by using spectroscopic and viscosity measurements. Results suggest that two of the complexes bind to DNA in an intercalative mode. Topoisomerase inhibition and DNA strand passage assay confirmed that two Ru (II) complexes act as efficient dual inhibitors of topoisomerases I and II by interference with the DNA religation. In MTT cytotoxicity studies, two Ru (II) complexes exhibit antitumor activity against BEL-7402, HeLa, MCF-7 and HepG2 tumor cells. Flow cytometry analysis shows an increase in the percentage of cells with apoptotic morphological features in the sub-G1 phase for Ru (II) complexes. Apoptosis induction has also been observed from AO/EB staining assay and Annexin V-FITC/PI double staining.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.64(06) [June2025]en_US
dc.subjectRuthenium (II) complexen_US
dc.subjectDNA-bindingen_US
dc.subjectTopoisomerase inhibitionen_US
dc.subjectCytotoxicityen_US
dc.subjectApoptosisen_US
dc.titleSynthesis, DNA binding, and dual topoisomerase I/II inhibitory activities of [Ru(tpy)(adtpy)]2+ and [Ru(dtp)(adtpy)]2+en_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v64i6.9991en_US
Appears in Collections:IJC Vol.64(06) [June 2025]

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