Pro-oxidant and antiproliferative effects of the 1,3,4-thiadiazole based Schiff base and its metal complexes

dc.authorscopusid35147160200
dc.authorscopusid57197424525
dc.authorscopusid22937820000
dc.authorscopusid6602447584
dc.authorscopusid14632863800
dc.authorscopusid7004903750
dc.authorscopusid7006501958
dc.contributor.authorTuran, Nevin
dc.contributor.authorTopçu, M.F.
dc.contributor.authorErgin, Z.
dc.contributor.authorSandal, S.
dc.contributor.authorTuzcu, M.
dc.contributor.authorAkpolat, N.
dc.contributor.authorYılmaz, B.
dc.date.accessioned2023-01-10T21:23:54Z
dc.date.available2023-01-10T21:23:54Z
dc.date.issued2011
dc.departmentFakülteler, Fen-Edebiyat Fakültesi, Kimya Bölümüen_US
dc.description.abstractAdverse biological activities of Schiff base (SB) derivatives are well known. In this study, the ligand and its metal complexes have been synthesized and characterized by IR, 1H-NMR spectra, elemental analyses, magnetic susceptibility, UV-Vis spectra, and thermogravimetry/differential thermal analysis. From the elemental analyses data, the complexes were proposed to have the general formula [Mn(L) 2(H 2O) 2], [Co(L) 2(H 2O) 2], and [Ni 2(L)(H 2O) 4(Cl) 3]. From the magnetic moment and UV-Vis spectra data, it was found that the geometrical structures of these complexes are octahedral. In the in vivo experiment, adult male rats were injected subcutaneously with a new SB (L) and its [Mn(L) 2(H 2O) 2], [Co(L) 2(H 2O) 2], and [Ni 2(L)(H 2O) 4(Cl) 3] complexes (25mg/kg body weight) and were then sacrificed 16 days later. Effects of these compounds on serum antioxidant vitamins (i.e., vitamins A, E, and C) and malondialdehyde (MDA) levels were measured in blood serum, liver, and kidney tissues. In an in vitro experiment, antiproliferative effects of these compounds were assessed on the human breast carcinoma MCF-7 and murine leukemia L1210 cell lines. Serum MDA and vitamins A, E, and C levels did not change by the treatments. However, in the kidney and liver tissues, MDA levels were higher, whereas vitamin levels were lower in treatment groups, compared to the control group. All compounds inhibited cell proliferation of MCF-7 and L1210 cancer cell lines in a dose-and time-dependent manner. In conclusion, SB derivatives tested in the current study induced oxidative stress in vivo and exhibited anti-proliferative effects in an in vitro culture system. © 2011 Informa Healthcare USA, Inc.en_US
dc.description.sponsorship522; 104T363en_US
dc.description.sponsorshipThis study was financially supported by TUBITAK (project no.: 104T363). The authors would also like to thank the Firat University Research Foundation for their financial support (FUBAP project no.: 522).en_US
dc.identifier.doi10.3109/01480545.2011.564177
dc.identifier.endpage378en_US
dc.identifier.issn0148-0545
dc.identifier.issue4en_US
dc.identifier.pmid21714772
dc.identifier.scopus2-s2.0-80052710275
dc.identifier.scopusqualityQ1
dc.identifier.startpage369en_US
dc.identifier.urihttps://doi.org/10.3109/01480545.2011.564177
dc.identifier.urihttps://hdl.handle.net/20.500.12639/5105
dc.identifier.volume34en_US
dc.identifier.wosWOS:000294861800005
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.institutionauthorTuran, Nevin
dc.language.isoen
dc.relation.ispartofDrug and Chemical Toxicologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject1;3;4-thiadiazole-based Schiff baseen_US
dc.subjectAntiproliferativeen_US
dc.subjectPro-oxidanten_US
dc.subject1,3,4 thiadiazole derivativeen_US
dc.subjectalpha tocopherolen_US
dc.subjectascorbic aciden_US
dc.subjectmalonaldehydeen_US
dc.subjectmetal complexen_US
dc.subjectretinolen_US
dc.subjectSchiff baseen_US
dc.subjectSchiff base derivativeen_US
dc.subjectunclassified drugen_US
dc.subjectanimal experimenten_US
dc.subjectarticleen_US
dc.subjectbreast carcinomaen_US
dc.subjectcancer cell cultureen_US
dc.subjectcell viabilityen_US
dc.subjectcontrolled studyen_US
dc.subjectdrug effecten_US
dc.subjectdrug synthesisen_US
dc.subjecthumanen_US
dc.subjecthuman cellen_US
dc.subjectin vitro studyen_US
dc.subjectin vivo studyen_US
dc.subjectinfrared spectrometryen_US
dc.subjectleukemia cell lineen_US
dc.subjectmaleen_US
dc.subjectnonhumanen_US
dc.subjectprooxidant propertyen_US
dc.subjectproton nuclear magnetic resonanceen_US
dc.subjectraten_US
dc.subjectthermogravimetryen_US
dc.subjectultraviolet spectroscopyen_US
dc.subjectAnimalsen_US
dc.subjectCell Line, Tumoren_US
dc.subjectCell Proliferationen_US
dc.subjectCoordination Complexesen_US
dc.subjectHumansen_US
dc.subjectKidneyen_US
dc.subjectLethal Dose 50en_US
dc.subjectLigandsen_US
dc.subjectLiveren_US
dc.subjectMaleen_US
dc.subjectMalondialdehydeen_US
dc.subjectMiceen_US
dc.subjectMolecular Structureen_US
dc.subjectOxidative Stressen_US
dc.subjectRatsen_US
dc.subjectRats, Wistaren_US
dc.subjectSchiff Basesen_US
dc.subjectThiadiazolesen_US
dc.subjectVitaminsen_US
dc.subjectMurinaeen_US
dc.subjectRattusen_US
dc.titlePro-oxidant and antiproliferative effects of the 1,3,4-thiadiazole based Schiff base and its metal complexesen_US
dc.typeArticle

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