The invention is directed to methods to inhibit TGF- and/or p38-
kinase using compounds of the formula
##STR1##
or the pharmaceutically acceptable salts thereof
wherein R3 is a noninterfering substituent;
each Z is CR2 or N, wherein no more than two Z positions
in ring A are N, and
wherein two adjacent Z positions in ring A cannot be N;
each R2 is independently a noninterfering substituent;
L is a linker;
n is 0 or 1; and
Ar is the residue of a cyclic aliphatic, cyclic heteroaliphatic,
aromatic or heteroaromatic moiety optionally substituted with 1-3 noninterfering substituents.