Inhibitors of Unactivated P38 MAP Kinase
Document Type
Article
Publication Date
12-1-2006
Abstract
Inhibition of the p38 map kinase pathway has been shown to be beneficial in the treatment of inflammatory diseases. The first class of potent p38 kinase inhibitors was the pyridinylimidazole compounds from SKB. Since then several pyridinylimidazole-based compounds have been shown to inhibit activated p38 kinase in vitro and in vivo. We have developed a novel series of pyridinylimidazole-based compounds, which potently inhibit the p38 pathway by binding to unactivated p38 kinase and only weakly inhibiting activated p38 kinase activity in vitro.
DOI
10.1016/j.bmcl.2006.08.101
Montclair State University Digital Commons Citation
Bullington, James; Argentieri, Dennis; Averill, Kristin; Carter, Demetrius; Cavender, Druie; Fahmy, Bohumila; Fan, Xiaodong; Hall, Daniel; Heintzelman, Geoffrey; Jackson, Paul; Fung-Leung, Wai Ping; Li, Xun; Ling, Ping; Olini, Gilbert; Razler, Thomas; Reuman, Michael; Rupert, Kenneth; Russell, Ronald; Siekierka, John; Wadsworth, Scott; Wolff, Russell; Xiang, Bangping; and Zhang, Yue Mei, "Inhibitors of Unactivated P38 MAP Kinase" (2006). Department of Chemistry and Biochemistry Faculty Scholarship and Creative Works. 159.
https://digitalcommons.montclair.edu/chem-biochem-facpubs/159