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J Med Chem ; 56(4): 1677-92, 2013 Feb 28.
Article in English | MEDLINE | ID: mdl-23350847

ABSTRACT

We describe the discovery of several pyrrolopyrazines as potent and selective Syk inhibitors and the efforts that eventually led to the desired improvements in physicochemical properties and human whole blood potencies. Ultimately, our mouse model revealed unexpected toxicity that precluded us from further advancing this series.


Subject(s)
Intracellular Signaling Peptides and Proteins/antagonists & inhibitors , Protein-Tyrosine Kinases/antagonists & inhibitors , Pyrazines/chemical synthesis , Pyrroles/chemical synthesis , Animals , B-Lymphocytes/drug effects , B-Lymphocytes/enzymology , Blood Proteins/metabolism , Crystallography, X-Ray , Humans , Mice , Microsomes, Liver/metabolism , Models, Molecular , Molecular Structure , Protein Binding , Pyrazines/pharmacology , Pyrazines/toxicity , Pyrroles/pharmacology , Pyrroles/toxicity , Structure-Activity Relationship , Syk Kinase
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