| Literature DB >> 23873737 |
Rhushikesh A Kulkarni1, Stephanie M Stanford, Nadeem A Vellore, Divya Krishnamurthy, Matthew R Bliss, Riccardo Baron, Nunzio Bottini, Amy M Barrios.
Abstract
We screened a small library of thiuram disulfides for inhibition of lymphoid tyrosine phosphatase (LYP) activity. The parent thiuram disulfide, disulfiram, inhibited LYP activity in vitro and in Jurkat T cells, whereas diethyldithiocarbamate failed to inhibit LYP at the concentrations tested. Compound 13, an N-(2-thioxothiazolidin-4-one) analogue, was found to be the most potent LYP inhibitor in this series, with an IC50 value of 3 μM. Compound 13 inhibits LYP pseudo-irreversibly, as evidenced by the time-dependence of inhibition, with a K(i) value of 1.1 μM and a k(inact) value of 0.004 s⁻¹. The inhibition of LYP by compound 13 could not be reversed significantly by incubation with glutathione or by prolonged dialysis, but could be partially reversed by incubation with dithiothreitol. Compound 13 also inhibited LYP activity in Jurkat T cells.Entities:
Keywords: PTP; disulfiram; inhibitors; screening; thiuram disulfides
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Year: 2013 PMID: 23873737 PMCID: PMC3863632 DOI: 10.1002/cmdc.201300215
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466