Journal
JOURNAL OF MEDICINAL CHEMISTRY
Volume 54, Issue 1, Pages 54-66Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jm101195a
Keywords
-
Categories
Ask authors/readers for more resources
A kinome-wide selectivity screen of > 20000 compounds with a rich representation of many structural classes has been completed Analysis of the selectivity patterns for each class shows that a broad spectrum of structural scaffolds can achieve specificity for many kinase families Kinase selectivity and potency are inversely correlated, a trend that is also found in a large set of kinase functional data Although selective and nonselective compounds are mostly similar in their physicochemical characteristics, we identify specific features that are present more frequently in compounds that bind to many kinases Our results support a scaffold-oriented approach for building compound collections to screen kinase targets
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available