| Literature DB >> 2393389 |
L H Elliott1, S E Wilkinson, A D Sedgwick, C H Hill, G Lawton, P D Davis, J S Nixon.
Abstract
The inhibition of phosphorylase kinase by a number of protein kinase inhibitors was examined. Both K252a and staurosporine are potent inhibitors of phosphorylase kinase with IC50 values of 1.7 nM and 0.5 nM respectively. K252a shows a 300-fold selectivity for this enzyme over protein kinase C whereas staurosporine shows only a 20-fold selectivity for phosphorylase kinase. In contrast, the Roche bis-indolyl maleimides inhibit phosphorylase kinase with IC50 values of approximately 1 microM and are highly selective for protein kinase C.Entities:
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Year: 1990 PMID: 2393389 DOI: 10.1016/0006-291x(90)91369-4
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575