摘要 |
Compounds of formula (1) are described in which R<SUP>a </SUP>and R<SUP>b </SUP>is each independently a hydrogen atom or a group R<SUP>c</SUP>, or R<SUP>a </SUP>and R<SUP>b </SUP>together form an oxo (-O) or thio (-S) group; X is a N atom or an optionally substituted CH group: Y is a -O- or -S- atom or -SO- or -SO<SUB>2</SUB>- group or an optionally substituted -CH<SUB>2</SUB>- or -NH- group with the proviso that when R<SUP>a </SUP>and R<SUP>b </SUP>together form an oxo (-O) or thio (-S) group Y is an optionally substituted -CH<SUB>2</SUB>- or -NH-group; L<SUP>1 </SUP>is a covalent bond or a linker atom or group; p is zero or the integer 1; Alk<SUP>1 </SUP>is an optionally substituted C<SUB>1-10</SUB>aliphatic or C<SUB>1-10</SUB>heteroaliphatic chain; n is zero the integer 1, 2 or 3 with the proviso that when n is zero Y is an optionally substituted -CH<SUB>2</SUB>- group; Ar is an optionally substituted C<SUB>6-12</SUB>aromatic or C<SUB>1-9</SUB>heteroaromatic group; m is zero or the integer 1, 2 or 3; q is zero or the integer 1 or 2; R<SUP>1</SUP>, R<SUP>c </SUP>and R<SUP>d </SUP>are hydrogen atoms or the substituents described in the patent specification; and the salts, solvates, hydrates and N-oxides thereof. The compounds are potent and selective inhibitors of p38 kinase and are useful in the treatment of immune or inflammatory disorders.
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