Please use this identifier to cite or link to this item: http://10.9.150.37:8080/dspace//handle/atmiyauni/2068
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dc.contributor.authorLunagariya, Miral V-
dc.contributor.authorThakor, Khyati P-
dc.contributor.authorVarma, Reena R-
dc.contributor.authorBhargav N, Waghela,-
dc.contributor.authorChandramani Pathak and Mohan N, Patel-
dc.date.accessioned2024-11-27T04:54:31Z-
dc.date.available2024-11-27T04:54:31Z-
dc.date.issued2017-12-11-
dc.identifier.urihttp://10.9.150.37:8080/dspace//handle/atmiyauni/2068-
dc.description.abstractSquare planar mononuclear platinumIJII) complexes were synthesized in the presence of neutral bidentate heterocyclic (5-quinoline 1,3,5-tri-substituted pyrazole scaffold) ligands and K2PtCl4 salt. The synthesized compounds were characterized by micro-elemental analysis, FT-IR, UV-vis, 1H NMR, 13C NMR, TGA, mass spectrometry and molar conductivity. Their biological activities were investigated by in vitro brine shrimp lethality bioassay, in vitro antimicrobial study against five different pathogens, in vivo cellular level cytotoxicity against Schizosaccharomyces pombe cells, and in vitro anti-proliferation assay. The binding constant Ksv, Kb, Ka values of the complexes were determined by DNA interaction studies. The gel electrophoresis assay was carried out to examine the effect of the complexes on the DNA nuclease of pUC19 plasmid DNA. The docking energies of the ligands (L1–L5) and complexes (I–V) were observed in the range of −265.14 to −284.33 kJ mol−1. The synthesized PtIJII) complexes (I–V) were screened against the MCF-7 (human breast adenocarcinoma) and HCT-116 (human colon carcinoma) cancer cell linesen_US
dc.language.isoenen_US
dc.subjectSynthesis of αen_US
dc.subjectβ unsaturateden_US
dc.subjectcarbonyen_US
dc.subjectcompoundsen_US
dc.titleSynthesis, characterization and biological application of 5-quinoline 1,3,5-trisubstituted pyrazole based platinumIJII) complexes†en_US
dc.typeArticleen_US
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