The present invention relates to novel 3,5-substituted 7-azaindole compounds of formula (I), their use in the inhibition of c-Jun N-terminal kinases, their use in medecine and particularly in the prevention and/or treatment of neurodegenerative disorders related to apoptosis and/or inflammation. The invention also provides processes for manufacture of said compounds, compositions containing them and processes for manufacturing such compositions. ##STR00001##

 
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> Piperidinylchromen-6-ylsulfonamide compounds as 5-hydroxytryptamine-6 ligands

> Compounds having 4-pyridylalkylthio group as substituent

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