Yarar, S.Öztürk, İbrahim İsmetBanti, Christina N.Panagiotou, NikosPapatriantafyllopoulou, C.Manoli, MariaHadjikakou, Sotiris K.2022-05-112022-05-1120180020-16931873-3255https://doi.org/10.1016/j.ica.2017.10.026https://hdl.handle.net/20.500.11776/7272Bismuth(III) complexes of the formulae [BiCl3(MBZT)(2)] center dot H2O} (1), {[BiCl2(mu(2)-Cl)(MMI)(2)](2)center dot(CH3)(2)CO} (2), {[BiCl3(mu(2)-S-PYT)(PYT)](2)} (3) {([BiCl2(MBZIM)(4)](+))center dot 2(Cl-) center dot(H3O+)center dot 2H(2)O} (4) and [BiCl3(tHPMT)(3)] (5) (where MBZT: 2-mercaptobenzothiazole, MMI: 2-mercapto-1-methylimidazole, PYT: 2-mercaptopyridine, MBZIM: 2-mercaptobenzimidazole, tHPMT: 2-mercapto-3,4,5,6-tetrahydro-pyrimidine) are reported. The compounds were characterized by spectroscopic techniques including FT-IR, FT-Raman, UV-Vis, H-1-, C-13-NMR spectroscopies, TG-DTA, e. a, molar conductivity and by single-crystal X-ray diffraction analysis. While 1, 4 and 5 are mononuclear compounds, 2 and 3 are dinuclear complexes in which the two Bi3+ ions are bridged through Cl- and SR groups respectively. Interestingly, 3 is the first example of dinuclear Bi3+ complex containing two Bi-(mu-SR)-Bi bridges between the two metal centers formed by covalent bonds. Compounds 1-5 were evaluated for their in vitro cytotoxic activity against human adenocarcinoma cervix (HeLa) and breast (MCF-7) cells. The toxicity of 1-5 was evaluated on normal human fetal lung fibroblast cells (MRC-5). The influence of 1-5, on the catalytic peroxidation of the linoleic acid by the enzyme lipoxygenase (LOX) was determined experimentally. (C) 2017 Elsevier B.V. All rights reserved.en10.1016/j.ica.2017.10.026info:eu-repo/semantics/closedAccessBiological Inorganic ChemistryDrug designBismuth(III) chlorideCell studiesLipoxygenase inhibitionAntimony(Iii) Halide-ComplexesBiological EvaluationCrystal-StructureStructural-CharacterizationMedicinal ChemistryIn-VitroLigands6-MercaptopurineThionesOrganotin(Iv)Synthesis, characterization and cytotoxic properties of bismuth(III) chloride complexes with heterocyclic thioamidesArticle4712333Q2WOS:0004198260000042-s2.0-85032497403Q2