Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/8834
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dc.rights.licenseopenAccess-
dc.contributor.authorTomović D.-
dc.contributor.authorBukonjić A.-
dc.contributor.authorKocovic, Aleksandar-
dc.contributor.authorNikolic, Milos-
dc.contributor.authorMijajlovic M.-
dc.contributor.authorJevtić, Verica-
dc.contributor.authorRatković, Zoran-
dc.contributor.authorArsenijevic A.-
dc.contributor.authorMilovanovic, Jelena-
dc.contributor.authorStojanovic B.-
dc.contributor.authorTrifunović, Srećko-
dc.contributor.authorRadic G.-
dc.date.accessioned2020-09-19T16:48:21Z-
dc.date.available2020-09-19T16:48:21Z-
dc.date.issued2017-
dc.identifier.issn1820-8665-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/8834-
dc.description.abstract© 2017, University of Kragujevac, Faculty of Science. All rights reserved. New complexes of copper(II) with S-alkenyl derivatives of thiosalicylic acid (alkenyl = propenyl-(L1), isobutenyl-(L2)) have been synthesized and characterized by microanalysis, infrared spectra, magnetic measurements, and by NMR spectra. The cytotoxic activity of two newly synthesized precursor S-alkenyl derivatives of thiosalicylic acid were tested using an MTT colorimetric technique on HCT-116 human colon carcinoma cells. The cytotoxic effect of the copper(II)- complexes were higher compared to the cytotoxicity of the corresponding ligand (for concentrations from 31.25 to 250 μM). Copper(II)-complexes showed a slightly lower cytotoxicity compared to cisplatin. Complexes of copper(II) with S-alkenyl derivatives of thiosalicylic acid (at concentrations from 250 to 1000 μM) had a cytotoxic effect on HCT-116 cells compared to cisplatin.-
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.sourceSerbian Journal of Experimental and Clinical Research-
dc.titleSynthesis, characterization, and cytotoxicity of binuclear copper(Ii)-complexes with some s-alkenyl derivatives of thiosalicylic acid-
dc.typearticle-
dc.identifier.doi10.1515/SJECR-2016-0071-
dc.identifier.scopus2-s2.0-85014810451-
Appears in Collections:Faculty of Medical Sciences, Kragujevac
Faculty of Science, Kragujevac

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