Show simple item record

dc.contributor.authorMahendiran, Dharmasivam
dc.contributor.authorPravin, Narayanaperumal
dc.contributor.authorBhuvanesh, Nattamai SP
dc.contributor.authorKumar, Raju Senthil
dc.contributor.authorViswanathan, Vijayan
dc.contributor.authorVelmurugan, Devadasan
dc.contributor.authorRahiman, Aziz Kalilur
dc.date.accessioned2020-12-04T02:59:25Z
dc.date.available2020-12-04T02:59:25Z
dc.date.issued2018
dc.identifier.issn2365-6549
dc.identifier.doi10.1002/slct.201800934
dc.identifier.urihttp://hdl.handle.net/10072/399954
dc.description.abstractA series of six new bis(thiosemicarbazone)copper(I) complexes of the type [Cu(L1–6)2Cl] (1−6) were synthesized and characterized. The complexes adopted trigonal planar ′Y′ shaped geometry coordinating through two thione sulphur atoms of two ligand molecules and one chloride ion. All the complexes intercalatively bind with calf thymus DNA (CT−DNA) as evidenced by spectral and molecular docking studies. The absorption and emission spectral techniques confirmed the strong interaction of the complexes with BSA via static quenching mode. The complexes efficiently cleave pBR322 DNA via hydrolytic pathway, and significantly interact with epidermal growth factor receptor. All the complexes were assessed for their anti‐proliferative activity, in which the complexes 2, 3 and 4 containing methyl, methoxy and hydroxyl groups, respectively, showed significant activity. The complexes induce apoptosis in EAC cells as evidenced by acridine orange (AO)/ethidium bromide (EB), Hoechst 33258 and propidium iodide (PI) staining methods, and cell cycle analysis. Cellular uptake studies revealed the ability of the complexes to go into the cytoplasm and accumulation in the cell nuclei. The complexes are involved in the generation of reactive oxygen species (ROS), mitochondrial mediated and caspase‐dependent apoptosis. Further, using a female Swiss albino mice model, we found that the complexes 2 and 3 inhibited Ehrlich ascites carcinoma (EAC) tumour cell growth in vivo.
dc.description.peerreviewedYes
dc.languageEnglish
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofpagefrom7100
dc.relation.ispartofpageto7111
dc.relation.ispartofissue25
dc.relation.ispartofjournalChemistrySelect
dc.relation.ispartofvolume3
dc.subject.fieldofresearchChemical sciences
dc.subject.fieldofresearchcode34
dc.subject.keywordsScience & Technology
dc.subject.keywordsPhysical Sciences
dc.subject.keywordsChemistry, Multidisciplinary
dc.subject.keywordsChemistry
dc.subject.keywordsCellular uptake
dc.titleBis(thiosemicarbazone)copper(I) Complexes as Prospective Therapeutic Agents: Interaction with DNA/BSA Molecules, and In Vitro and In Vivo Anti-Proliferative Activities
dc.typeJournal article
dc.type.descriptionC1 - Articles
dcterms.bibliographicCitationMahendiran, D; Pravin, N; Bhuvanesh, NSP; Kumar, RS; Viswanathan, V; Velmurugan, D; Rahiman, AK, Bis(thiosemicarbazone)copper(I) Complexes as Prospective Therapeutic Agents: Interaction with DNA/BSA Molecules, and In Vitro and In Vivo Anti-Proliferative Activities, ChemistrySelect, 2018, 3 (25), pp. 7100-7111
dc.date.updated2020-12-04T02:58:13Z
gro.hasfulltextNo Full Text
gro.griffith.authorDharmasivam, Mahendiran


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

  • Journal articles
    Contains articles published by Griffith authors in scholarly journals.

Show simple item record