| Literature DB >> 17532514 |
Abstract
Small molecule inhibitors of protein tyrosine kinases have become both powerful chemical probes of biological processes and clinically effective therapeutics. In contrast, few small molecule inhibitors of protein tyrosine phosphatases have been identified and none are currently approved for clinical use. New cell-based high-content methods have been developed that should enable investigators to probe for selective inhibitors of diseases-relevant protein phosphatases. Details of these methods are described herein.Mesh:
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Year: 2007 PMID: 17532514 PMCID: PMC1950282 DOI: 10.1016/j.ymeth.2007.02.006
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608