2014
DOI: 10.1089/ars.2013.5720
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Protein Tyrosine Phosphatase Inhibition by Metals and Metal Complexes

Abstract: Investigating the structural basis of the interactions between metal complexes and PTPs would facilitate a comprehensive understanding of the structure-activity relationship and accelerate the development of promising metal-based drugs targeting specific PTPs.

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Cited by 41 publications
(37 citation statements)
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“…Interestingly, in contrast to what we observed for 7, other Ru-arene complexes of the (p-cymene)(NHC)RuCl 2 type have been reported to be good inhibitors of TrxR [65]. Moreover, the cathepsins cysteine proteases have been shown to be inhibited by other families of Ru-arene complexes, [31] while protein tyrosine phosphatases are good targets for Cu compounds [66].…”
Section: Enzyme Inhibition Studiescontrasting
confidence: 88%
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“…Interestingly, in contrast to what we observed for 7, other Ru-arene complexes of the (p-cymene)(NHC)RuCl 2 type have been reported to be good inhibitors of TrxR [65]. Moreover, the cathepsins cysteine proteases have been shown to be inhibited by other families of Ru-arene complexes, [31] while protein tyrosine phosphatases are good targets for Cu compounds [66].…”
Section: Enzyme Inhibition Studiescontrasting
confidence: 88%
“…The gold(I) mono-and polynuclear compounds were also shown to be potent TrxR inhibitors in the nM range in vitro. In the case of the mononuclear Cu(II) complex 6 the fact that there is no correlation between its marked cytotoxic activity and the poor TrxR inhibition is not unexpected, since other mechanisms are known to be responsible for Cu(II) complex cytotoxic effects, including the inhibition of protein tyrosine phosphatases [66] and the influence on cell redox pathways, [67,68] as well as DNA damage [69].…”
Section: Discussionmentioning
confidence: 99%
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“…Their copper complexes can inhibit the activity of protein tyrosine phosphatase (Lu & Zhu, 2014). Thus, we reacted 2,5-bis(1H-1,2,4-triazol-1-yl)terephthalic acid with CuCl 2 under hydrothermal conditions in an attempt to form a complex, but instead crystals of the title compound, (I), were obtained.…”
Section: Structure Descriptionmentioning
confidence: 99%
“…These observations suggest that the complexes show some selectivity towards certain PTPs compared to others. There also seems to be an effect on the inhibitory properties of the complex on increasing the length of the linker from diethanolamine (14) to dipropanolamine (15) Table 2. We also carried out the inhibition studies using VOSO 4 as a control.…”
Section: Phosphatase Inhibition Assaysmentioning
confidence: 99%