| Literature DB >> 21426149 |
Abstract
Several 'classical' protein tyrosine phosphatases are attractive therapeutic targets, including PTP1B for obesity and Type II diabetes; SHP2 for cancer and Lyp for rheumatoid arthritis. Progress has been made in identifying a broad range of chemically distinct inhibitors; however, developing selective and cell-permeable clinically useful compounds has proved challenging. Here the ongoing challenges and recent significant advances in the field are reviewed. Key novel compounds are highlighted and a perspective on the future of phosphatase inhibitor development is presented.Entities:
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Year: 2010 PMID: 21426149 DOI: 10.4155/fmc.10.241
Source DB: PubMed Journal: Future Med Chem ISSN: 1756-8919 Impact factor: 3.808