107833-28-3Relevant articles and documents
Structure-based design of novel Chk1 inhibitors: Insights into hydrogen bonding and protein-ligand affinity
Foloppe, Nicolas,Fisher, Lisa M.,Howes, Rob,Kierstan, Peter,Potter, Andrew,Robertson, Alan G. S.,Surgenor, Allan E.
, p. 4332 - 4345 (2005)
We report the discovery, synthesis, and crystallographic binding mode of novel furanopyrimidine and pyrrolopyrimidine inhibitors of the Chk1 kinase, an oncology target. These inhibitors are synthetically tractable and inhibit Chk1 by competing for its ATP
METHODS FOR THE TREATMENT OF DISORDERS RELATED TO PHOSPHORYLATION OF HISTONES
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Paragraph 0115; 0116, (2016/04/26)
Methods for disease diagnosis, prognosis and therapy selection. Compositions for use in these methods and selected therapies for treatment are also disclosed.