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Published in 2019 at "MedChemComm"
DOI: 10.1039/c9md00175a
Abstract: Thienopyridone (TP) has been proposed as a selective inhibitor of phosphatases of regenerating liver (PRL or PTP4A). PRLs are dual specificity phosphatases that promote cancer progression and are attractive anticancer targets. TP and iminothienopyridinedione (ITP),…
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Keywords:
mechanism thienopyridone;
protein phosphatases;
thienopyridone;
inhibition ... See more keywords