| 摘要 |
The invention relates to isoxazolopyridone derivatives of a formula (I-a): wherein R<1a >represents an optionally-substituted heteroaryl or phenyl group, R<2a >represents an optionally-substituted phenyl or heteroaryl group, and R<3a >represents a methyl group, provided that, (1) when R<1a >is an unsubstituted phenyl group, then R<2a >must not be a para-substituted phenyl group of which the substituent is any of a methoxy group, a chloro group, a methyl group, a trifluoromethyl group, a fluoro group, a bromomethyl group or a dimethylaminomethyl group, and R<2a >must not be an unsubstituted heteroaryl group, and (2) when R<1a >is a 4-tolyl group or a 4-fluorophenyl group, then R<2a >must not be an unsubstituted phenyl group, a 4-methoxyphenyl group or a 4-fluorophenyl group, or their pharmaceutically-acceptable salts. The isoxazolopyridone derivatives or their pharmaceutically-acceptable salts of the invention have a metabotropic glutamic acid receptor-antagonistic effect, and are useful for remedy of, for example, anxiety disorders, psychosomatic disorders, obsessive-compulsive neurosis, bipolar disorders, melancholia, eating disorders, schizophrenia, multi-infarct dementia, Alzheimer disease, epilepsy, Parkinson disease, Huntington's chorea, pain or retrograde neurosis.
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