摘要 |
The present invention provides a novel compound exhibiting an excellent inhibitory action on AMPA receptor and/or kainate receptor. That is, it provides a compound represented by the following formula, a salt thereof or a hydrate of them. In the formula, A<SUP>1</SUP>, A<SUP>2 </SUP>and A<SUP>3 </SUP>are independent of each other and each represents a C<SUB>3-8 </SUB>cycloalkyl group, a C<SUB>3-8 </SUB>cycloalkenyl group, a 5- to 14-membered non-aromatic heterocyclic group, a C<SUB>6-14 </SUB>aromatic hydrocarbon cyclic group or a 5- to 14-membered aromatic heterocyclic group, each of which may be substituted; Q represents O, S or NH; Z represents C or N; X<SUP>1</SUP>, X<SUP>2 </SUP>and X<SUP>3 </SUP>are independent of each other and each represents a single bond, an optionally substituted C<SUB>1-6 </SUB>alkylene group, an optionally substituted C<SUB>2-6 </SUB>alkenylene group, an optionally substituted C<SUB>2-6 </SUB>alkynylene group, -NH-, -O-, -NHCO-, -CONH-, -SO<SUB>0-2</SUB>-, etc.; R<SUP>1 </SUP>and R<SUP>2 </SUP>are independent of each other and each represents a hydrogen atom or an optionally substituted C<SUB>1-6 </SUB>alkyl group, or R<SUP>1 </SUP>and R<SUP>2 </SUP>may be bound together such that CR<SUP>2</SUP>-ZR<SUP>1 </SUP>forms C-C; and R<SUP>3 </SUP>represents a hydrogen atom or an optionally substituted C<SUB>1-6 </SUB>alkyl group etc., or may be bound to any atom in A<SUP>1 </SUP>or A<SUP>3 </SUP>to form, together with the atom, an optionally substituted C<SUB>5-8 </SUB>hydrocarbon ring or an optionally substituted 5- to 8-membered heterocyclic ring.
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