摘要 |
The present invention relates to a carboxylic acid compound of formula (I): wherein R<SUP>1 </SUP>is H, alkyl; m is 2, 3; n is 0-2; R<SUP>2 </SUP>is phenyl, naphthyl, benzofuran, benzothiophene; Q is -CH<SUB>2</SUB>-O-Cyc1, -CH<SUB>2</SUB>-Cyc2, -L-Cyc3; R<SUP>3a </SUP>and R<SUP>3b </SUP>each independently is hydrogen, alkyl or taken together form tetrahydro-2H-pyran; a pharmaceutically acceptable salt thereof, a method for producing a process of the preparation thereof and a pharmaceutical agent comprising the same as an active ingredient. The compound of formula (I) have an antagonizing activity against PGE<SUB>2 </SUB>receptor, specifically EP<SUB>3 </SUB>receptor which is subtype thereof, and are useful for the prevention and/or treatment of itching, pain, urinary disturbance or stress disease.
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