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Mutat Res ; 224(1): 89-94, 1989 Sep.
Article in English | MEDLINE | ID: mdl-2671715

ABSTRACT

The mutagenicity of thiol (SH)-containing compounds was tested in Salmonella typhimurium TA102 in the liquid preincubation method. Cysteinyl-glycine (CG), cysteine ethyl ester (CEE), L- and D-penicillamine (PA), cysteine (Cys) and glutathione (GSH) were mutagenic to strain TA102 without metabolic activation. On a molar basis, CG was the most potent mutagen. The mutagenicity of the remaining compounds decreased in the order specified above. The mutagenic response of each thiol-containing compound was a function of the pKa of the thiol group and the pH of the preincubation mixture. This indicates that a thiolate anion, rather than a free thiol, is required for mutagenesis.


Subject(s)
Mutagens , Salmonella typhimurium/genetics , Sulfhydryl Compounds/toxicity , Chemical Phenomena , Chemistry , Cysteine/analogs & derivatives , Cysteine/toxicity , Dipeptides/toxicity , Glutathione/toxicity , Hydrogen-Ion Concentration , Mutagenicity Tests , Penicillamine/toxicity
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