CELL BIOLOGY INTERNATIONAL, cilt.28, ss.267-272, 2004 (SCI İndekslerine Giren Dergi)
3-substituted-2-thiohydantoin derivatives were synthesized and their Structures elucidated by IR, H-1-NMR spectroscopy and elemental analysis. The cytotoxicity of the 2-thiohydantoin derivatives to rat embryo fibroblasts (F2408) in vitro was determined, and the effects of these compounds on intracellular free Ca2+, [Ca2+](i) were measured by spectrofluorophotometry. Cytotoxicity was determined by metabolic reduction of a tetrazolium salt to a formazan dye (MTT assay). Compounds 4 and 7 showed cytotoxic activity, with IC50 values in the range of 1-1.2 muM. Introduction of either chlorophenyl, metoxyphenyl, nitrophenyl or benzyl groups at C-3 resulted in concentration-dependent cytotoxic effects. Compounds 1-6 at 1 muM or more significantly increased [Ca2+](i) in a dose-dependent manner in the cultured fibroblasts. This action may have been mediated through intracellular calcium stores. (C) 2004 Elsevier Ltd. All rights reserved.