Aryl-substituted pyrazole-amide compounds useful as kinase inhibitors

   
   

The present invention relates to compounds having the formula, 1 and pharmaceutically-acceptable salts, prodrugs, solvates, isomers, and/or hydrates thereof, wherein Q is an optionally-substituted phenyl, pyridyl, pyridazinyl, pyrimidinyl, or pyrazinyl ring; R.sub.2 is alkyl or an amino group as defined herein; and Z is optionally-substituted oxadiazolyl or --C(.dbd.O)NR.sub.6, wherein R.sub.6 is lower alkyl or cyclopropyl. The compounds are surprisingly advantageous in preparing pharmaceutical compositions for treating p38 kinase related conditions and/or in methods of treating conditions associated with the activity of p38 kinase in a patient.

 
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