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dc.creatorJoksović, M.D.
dc.creatorMarković, V.
dc.creatorJuranić, Zorica
dc.creatorStanojković, Tatjana
dc.creatorJovanović, L.S.
dc.creatorDamljanović, I.S.
dc.creatorSzécsényi, K.M.
dc.creatorTodorović, Nina
dc.creatorTrifunović, Snežana
dc.creatorVukićević, R.D.
dc.date.accessioned2019-01-30T17:22:04Z
dc.date.available2019-01-30T17:22:04Z
dc.date.issued2009
dc.identifier.issn0022-328X
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/619
dc.description.abstractA series of new N-[(3-ferrocenyl-1-phenylpyrazol-4-yl)methyl] α-amino acids were prepared and characterized by a range of spectroscopic techniques and cyclic voltammetry. The in vitro antitumor activity of all synthesized compounds was investigated against cervix adenocarcinoma HeLa, melanoma Fem-x and myelogenous leukemia K562 cell lines using the MTT method. Tryptophan derivative 1l exhibited the highest cytotoxic activity in the cell growth inhibition of all three types of cell lines.en
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/142028/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/142042/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/145006/RS//
dc.rightsrestrictedAccess
dc.sourceJournal of Organometallic Chemistry
dc.subjectAmino acidsen
dc.subjectcytotoxicityen
dc.subjectFerrocenyl pyrazoleen
dc.titleSynthesis, characterization and antitumor activity of novel N-substituted α-amino acids containing ferrocenyl pyrazole-moietyen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractВукићевић, Р.Д.; Марковић, В.; Јуранић, З.Д.; Тодоровић, Нина; Трифуновић, С.; Јоксовић, М.Д.; Станојковић, Т.; Јовановић, Л.С.; Дамљановић, И.С.; Сзéцсéнyи, К.М.;
dc.citation.volume694
dc.citation.issue24
dc.citation.spage3935
dc.citation.epage3942
dc.citation.other694(24): 3935-3942
dc.citation.rankM22
dc.identifier.doi10.1016/j.jorganchem.2009.08.013
dc.identifier.rcubConv_4222
dc.identifier.scopus2-s2.0-70349999659
dc.identifier.wos000271099300015
dc.type.versionpublishedVersion


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