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Synthesis, characterization and biological application of 5-quinoline 1,3,5-trisubstituted pyrazole based platinumIJII) complexes†

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dc.contributor.author Lunagariya, Miral V
dc.contributor.author Thakor, Khyati P
dc.contributor.author Varma, Reena R
dc.contributor.author Bhargav N, Waghela,
dc.contributor.author Chandramani Pathak and Mohan N, Patel
dc.date.accessioned 2024-11-27T04:54:31Z
dc.date.available 2024-11-27T04:54:31Z
dc.date.issued 2017-12-11
dc.identifier.uri http://10.9.150.37:8080/dspace//handle/atmiyauni/2068
dc.description.abstract Square 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 lines en_US
dc.language.iso en en_US
dc.subject Synthesis of α en_US
dc.subject β unsaturated en_US
dc.subject carbony en_US
dc.subject compounds en_US
dc.title Synthesis, characterization and biological application of 5-quinoline 1,3,5-trisubstituted pyrazole based platinumIJII) complexes† en_US
dc.type Article en_US


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