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1.
J Inorg Biochem ; 22(1): 65-72, 1984 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-6092535

RESUMO

1-Octanol/water partition coefficients, [HgII]octanol/[HgII]water, provide a simple but limited model system for aspects of the biological behavior of methylmercury(II) and commonly used organomercury(II) medicinal compounds. In an octanol/water system some widely studied antidotes for mercury poisoning at least partly displace the biological thiols L-cysteine and glutathione from binding to MeHgII at pH 6.9. Addition of the antidote meso-dimercaptosuccinic acid to MeHgII in the presence of glutathione results in formation of metallic mercury. For RHgII derivatives of L-cysteine and glutathione, octanol/water partition coefficients follow the order Ph greater than Et greater than Me. An exceptionally high value for diphenylmercury, compared with PhHgII derivatives of L-cysteine and glutathione, is consistent with reported results of the distribution of mercury compounds in rats. Ethylmercury(II) is partly displaced from thimerosal by L-cysteine and glutathione in the octanol/water system, indicating that the active form of thimerosal in vivo may involve binding of EtHgII to biological ligands.


Assuntos
Antídotos , Compostos de Metilmercúrio/intoxicação , Modelos Biológicos , Octanóis , Compostos Organomercúricos , Água , Animais , Antídotos/metabolismo , Fenômenos Químicos , Físico-Química , Cisteína/metabolismo , Compostos de Etilmercúrio/metabolismo , Glutationa/metabolismo , Compostos de Metilmercúrio/metabolismo , Compostos Organomercúricos/metabolismo , Compostos de Fenilmercúrio/metabolismo , Ratos , Succímero/metabolismo
2.
J Inorg Biochem ; 19(4): 319-27, 1983 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-6655472

RESUMO

Methylmercury(II) complexes of the most widely studied antidotes for mercury poisoning have been prepared, and both the water solubility and 1-octanol/water partition coefficients determined for these complexes and the L-cysteine complex. New complexes of N-acetyl-D,L-penicillamine, 2-mercaptosuccinic acid, meso-dimercaptosuccinic acid, and Unithiol have been synthesized and characterized, and are found to have the formulations MeHgSCMe2CH(NHCOMe)CO2H, MeHgSCH(CO2H)CH2CO2H, MeHgSCH(CO2H)CH(CO2H)SHgMe, and Na[MeHgSCH2CH-(SHgMe)CH2SO3], respectively. Trends in octanol/water partition coefficients are consistent with reported studies of the effectiveness of antidotes for MeHg(II) poisoning and redistribution of MeHg(II) on administration of antidotes, particularly for British anti-Lewisite, Unithiol, and meso-dimercaptosuccinic acid.


Assuntos
Antídotos/síntese química , Quelantes/síntese química , Compostos de Metilmercúrio/intoxicação , Humanos , Solubilidade
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