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dc.contributor.authorOzturk, I.en
dc.contributor.authorFilimonova, S.en
dc.contributor.authorHadjikakou, Sotiris K.en
dc.contributor.authorKourkoumelis, Nikolaosen
dc.contributor.authorDokorou, Vaso N.en
dc.contributor.authorManos, Manolis J.en
dc.contributor.authorTasiopoulos, Anastasios J.en
dc.contributor.authorBarsan, M. M.en
dc.contributor.authorButler, I. S.en
dc.contributor.authorMilaeva, E. R.en
dc.contributor.authorBalzarini, J.en
dc.contributor.authorHadjiliadis, Nicken
dc.creatorOzturk, I.en
dc.creatorFilimonova, S.en
dc.creatorHadjikakou, Sotiris K.en
dc.creatorKourkoumelis, Nikolaosen
dc.creatorDokorou, Vaso N.en
dc.creatorManos, Manolis J.en
dc.creatorTasiopoulos, Anastasios J.en
dc.creatorBarsan, M. M.en
dc.creatorButler, I. S.en
dc.creatorMilaeva, E. R.en
dc.creatorBalzarini, J.en
dc.creatorHadjiliadis, Nicken
dc.date.accessioned2019-11-21T06:21:50Z
dc.date.available2019-11-21T06:21:50Z
dc.date.issued2010
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55927
dc.description.abstractEight new antimony(III) iodide complexes of the heterocyclic thioamides, 2-mercapto-1-methylimidazole (MMI), 2-mercaptobenzlmidazole (MBZIM), 5-ethoxy-2-mercaptobenzimldazole (EtMBZIM), 2-mercaptothiazolidine (MTZD), 3-methyl-2-mercaptobenzothiazole (NMeMBZT), 2-mercapto-3,4,5,6- tetrahydropyrlmidine (tHPMT), 2-mercaptopyrldlne (PYT), and 2-mercaptopyrimldlne (PMT) of formulas {[Sbl3(MMl)2] -MeOH} (1), [Sbl 3(MBZIM)2] (2), {[Sbl2(μ2-I) (EtMBZIM)2]2-H2O} (3), [Sbl3(MTZD)] (4), [(NMeMBZT)Sbl2(μ2-I)2(μ2- S-NMeMBZT)Sbl2 (NMeMBZT)] (5), {[Sbl3OHPMT) 3]-MeOH} (6), [Sbl3(PYT)] (7) and [Sbl3(PMT) 2] (8), have been synthesized and characterized by elemental analysis, FT-IR spectroscopy, FT-Raman spectroscopy and TG-DTA analysis. The crystal structures of 3,4,5,6, and 7 were also determined by X-ray diffraction. The complexes show interesting structural motifs. Complex 6 is a monomer, with octahedral (Oh) geometry around the metal ion formed by three sulfur and three iodide atoms. Complexes 3 and 5 are dimers, with a square pyramidal (SP) geometry in each monomeric unit, while complexes 4 and 7 are polymers with pseudotrlgonal bipyramidal (ψ-TBP). Two or three sulfur atoms from thioamide ligands and three iodide atoms are bound to Sb atoms forming building blocks for the dimers and polymers. Strong intramolecular interactions between μ2-I and/or μ2-S and Sb atoms stabilize both structures. In dimer complex 5, two terminal iodide and one terminal sulfur atom are bonded to the Sb ion, while two μ2-I and one μ2-S bridging atoms bridge the metal Ions forming ψ-Oh geometry. Computational studies using multivariant linear regression (MLR) and artificial neural networks (ANN) and considering biological results (50% inhibitory concentration, IC50) as dependent variables derived a theoretical equation for IC50 values of the complexes studied. The calculated IC50 values are compared satisfactorily with the experimental inhibitory activity of the complexes measured. Complexes 3 - 7 were used to study their influence upon the catalytic peroxidation of linoleic acid by the enzyme Lipoxygenase (LOX). Compounds 1 - 8 were also tested for In vitro cytotoxicity, and they showed mostly a moderate cytostatic activity against a variety of tumor cell lines but comparable with those found for the antimony(III) chloride and bromide complexes, reported earlier [Ozturk et al. Inorg. Chem. 2007, 46, 2861-2866en
dc.description.abstractOzturk et al. Inorg. Chem. 2009, 48, 2233-2245]. © 2009 American Chemical Society.en
dc.sourceInorganic chemistryen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-74549119472&doi=10.1021%2fic901442e&partnerID=40&md5=6b6e2100baba2352f44ac4ff2f128c84
dc.subjectarticleen
dc.subjecthumanen
dc.subjectNeoplasmsen
dc.subjectHumansen
dc.subjectdrug effecten
dc.subjectneoplasmen
dc.subjectmetabolismen
dc.subjectAnimalsen
dc.subjectanimalen
dc.subjectcell survivalen
dc.subjectchemistryen
dc.subjectcytostatic agenten
dc.subjectchemical structureen
dc.subjectX ray crystallographyen
dc.subjectantimonyen
dc.subjecttumor cell lineen
dc.subjectCell Line, Tumoren
dc.subjectModels, Molecularen
dc.subjectCrystallography, X-Rayen
dc.subjectiodideen
dc.subjectIodidesen
dc.subjectlipoxygenaseen
dc.subjectCytostatic Agentsen
dc.subjectthioketoneen
dc.subjectThionesen
dc.titleStructural motifs and biological studies of new antimony(iii) iodide complexes with thionesen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1021/ic901442e
dc.description.volume49
dc.description.issue2
dc.description.startingpage488
dc.description.endingpage501
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :36</p>en
dc.source.abbreviationInorg.Chem.en
dc.contributor.orcidTasiopoulos, Anastasios J. [0000-0002-4804-3822]
dc.contributor.orcidHadjikakou, Sotiris K. [0000-0001-9556-6266]
dc.gnosis.orcid0000-0002-4804-3822
dc.gnosis.orcid0000-0001-9556-6266


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