Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/10258
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dc.contributor.authorRatković, Zoran-
dc.contributor.authorJuranić Z.-
dc.contributor.authorStanojkovic, Tatjana-
dc.contributor.authorManojlović, Dragan-
dc.contributor.authorVukicevic R.-
dc.contributor.authorRadulovic, Niko-
dc.contributor.authorJoksović, Milan-
dc.date.accessioned2021-04-20T15:16:55Z-
dc.date.available2021-04-20T15:16:55Z-
dc.date.issued2010-02-01-
dc.identifier.issn00452068-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/10258-
dc.description.abstractA series of new α,β-unsaturated conjugated ketones containing ferrocenyl pyrazole unit were synthesized and fully characterized by IR and NMR spectroscopy. Electrochemical characterization of subject compounds was performed by means of cyclic voltametry. The in vitro cytotoxic activity of all the synthesized compounds was studied against cervix adenocarcinoma HeLa, melanoma Fem-x and myelogenous leukemia K562 cell lines by the MTT method. Derivative 1l containing 3-pyridyl moiety exhibited a better cytotoxic activity in the cell growth inhibition of K562 cell lines in comparison with cisplatin as a reference compound. © 2009 Elsevier Inc. All rights reserved.-
dc.relation.ispartofBioorganic Chemistry-
dc.titleSynthesis, characterization, electrochemical studies and antitumor activity of some new chalcone analogues containing ferrocenyl pyrazole moiety-
dc.typearticle-
dc.identifier.doi10.1016/j.bioorg.2009.09.003-
dc.identifier.scopus73349113168-
Appears in Collections:Faculty of Science, Kragujevac

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