Abstract
Much effort has been expended to develop inhibitors against protein-tyrosine phosphatases (PTPs), nearly all of it unsuccessful. A recent report, describing a highly specific, orally bioavailable inhibitor of the PTP oncoprotein SHP2 with in vivo activity, suggests that allostery might provide a way forward for PTP inhibitor development.
Copyright © 2016 Elsevier Inc. All rights reserved.
MeSH terms
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Animals
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Humans
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Mice
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Molecular Targeted Therapy
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Neoplasms / drug therapy*
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Neoplasms / enzymology
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Neoplasms / genetics
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Protein Kinase Inhibitors / pharmacology*
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Protein Tyrosine Phosphatase, Non-Receptor Type 11 / antagonists & inhibitors*
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Protein Tyrosine Phosphatase, Non-Receptor Type 11 / genetics
Substances
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Protein Kinase Inhibitors
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Protein Tyrosine Phosphatase, Non-Receptor Type 11