http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2013331378-A1

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inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b570521184cb13926c9b38f2b7e936af
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publicationDate 2013-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2013331378-A1
titleOfInvention Pyrazolopyridine derivative or pharmacologically acceptable salt thereof
abstract A pyrazolopyridine derivative represented by the following formula (I) or a pharmacologically acceptable salt thereof exhibits a strong EP 1 receptor antagonistic effect. Thus, the derivative or the pharmacologically acceptable salt is useful as a therapeutic agent for lower urinary tract symptoms (LUTS), particularly, overactive bladder syndrome (OABs), or a prophylactic agent therefor and furthermore, is also useful in the treatment, prevention, or suppression of various pathological conditions in which the EP 1 receptor is involved, such as inflammatory disease, pain disease, osteoporosis, and cancer. n n n n n n n n n n [A is a benzene ring or the like, Y 1 is C 1-6 alkylene, R 1 is —C(═O)—OZ 1 or the like, Z 1 is H or the like, R 2 is a branched C 3-6 alkyl group or the like, R 3 is H or the like, R 4 is a hydrogen atom or the like, and R 5 is a hydrogen atom or the like].
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112892436-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2016038890-A1
priorityDate 2011-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 4145.