Молимо вас користите овај идентификатор за цитирање или овај линк до ове ставке: https://scidar.kg.ac.rs/handle/123456789/10258
Пун извештај метаподатака
Поље DC-а ВредностЈезик
dc.rights.licenserestrictedAccess-
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-
dc.identifier.issn0045-2068-
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.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.sourceBioorganic 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.scopus2-s2.0-73349113168-
Налази се у колекцијама:Faculty of Science, Kragujevac

Број прегледа

741

Број преузимања

16

Датотеке у овој ставци:
Датотека Опис ВеличинаФормат 
PaperMissing.pdf
  Ограничен приступ
29.86 kBAdobe PDFСличица
Погледајте


Ставке на SCIDAR-у су заштићене ауторским правима, са свим правима задржаним, осим ако није другачије назначено.