Pyrimidine analogs of the pyridinylimidazole class of CSBP/p38 kinase inhib
itors were prepared in an effort to reduce the potent inhibition of hepatic
cytochrome P450 observed for the pyridinyl compounds. The substitution of
pyrimidin-4-yl, 2-methoxypyrimidin-4-yl, or 2-methylaminopyrimidin-4-yl for
pyridin-4-yl effectively dissociates CSBP/p38 kinctse from P450 inhibition
for this series and furthermore achieves an increase in oral activity. (C)
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