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S-(N-benzylthiocarbamoyl)cysteine

Known as: S-(N-benzylthiocarbamoyl)-L-cysteine, benzylisothiocyanate cysteine conjugate 
National Institutes of Health

Related topics

Related topics

3 relations

Broader (2)

CysteineThiocyanates
analogs & derivatives

Papers overview

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Highly Cited
2001
Highly Cited
2001
Involvement of glutathione metabolism in the cytotoxicity of the phenethyl isothiocyanate and its cysteine conjugate to human leukaemia cells in vitro.
Highly Cited
1998
Highly Cited
1998
Immunostimulation of murine spleen cells by materials associated with bovine milk protein fractions.
Purified bovine milk proteins that were added to cultures of murine spleen cells significantly increased cell proliferation and… 
Highly Cited
1996
Highly Cited
1996
Heteroatom-substituted analogues of the active-site directed inhibitor estra-1,3,5(10)-trien-17-one-3-sulphamate inhibit estrone sulphatase by a different mechanism
Highly Cited
1996
Highly Cited
1996
Synthesis, redox properties, in vivo formation, and neurobehavioral effects of N-acetylcysteinyl conjugates of dopamine: possible metabolites of relevance to Parkinson's disease.
A very early event in the pathogenesis of idiopathic Parkinson's disease (PD) has been proposed to be an elevated translocation… 
1996
1996
Inhibition of human leukaemia 60 cell growth by mercapturic acid metabolites of phenylethyl isothiocyanate.
1992
1992
Metabolic oxidation and toxification of N-methylformamide catalyzed by the cytochrome P450 isoenzyme CYP2E1.
Alkylformamides, for example N-methylformamide, are hepatotoxic in rodents and humans. The mechanism by which N-methylformamide… 
1990
1990
Stimulation of a human erythrocyte membrane ATPase by glutathione conjugates.
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