摘要 |
Medicament being useful as a fibrosis inhibitor for organs or tissues, which comprises a compound of the formula (I): wherein Ring Z is optionally substituted pyrrole ring, etc.; W<SUP>2 </SUP>is -CO-, -SO<SUB>2</SUB>-, optionally substituted C<SUB>1</SUB>-C<SUB>4 </SUB>alkylene, etc.; Ar<SUP>2 </SUP>is optionally substituted aryl, etc.; W<SUP>1 </SUP>and Ar<SUP>1 </SUP>mean the following (1) and (2): (1) W<SUP>1 </SUP>is optionally substituted C<SUB>1</SUB>-C<SUB>4 </SUB>alkylene, etc.; Ar<SUP>1 </SUP>is optionally substituted bicyclic heteroaryl having 1 to 4 nitrogen atoms as ring-forming atoms: (2) W<SUP>1 </SUP>is optionally substituted C<SUB>2</SUB>-C<SUB>5 </SUB>alkylene, optionally substituted C<SUB>2</SUB>-C<SUB>5 </SUB>alkenylene, etc.; and Ar<SUP>1 </SUP>is aryl or monocyclic heteroaryl, which is substituted by carboxyl, alkoxycarbonyl, etc. at the ortho- or meta-position thereof with respect to the binding position of W<SUB>1</SUB>, or a pharmaceutically acceptable salt thereof.
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