http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2004123539-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P13-12
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filingDate 2001-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_53cbe1d3b272cfddd532beb2449cdcf5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e185cc7a48225552f862ef70088aa934
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publicationDate 2004-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2004123539-A
titleOfInvention New pyrazolopyridine compounds and pharmaceutical uses
abstract SOLUTION: General formula (1) Embedded image [Wherein, R 1 , R 2 and R 3 are a C 1-6 alkyl group or the like; R 4 is a hydrogen atom or the like; R 5 and R 6 are the same or different and are a hydrogen atom, a C 1-6 alkyl group, C 1-6 alkoxy group, a halogen atom or the like; X is -NH -, - O -, - CH 2 - be like; Y is an -NH- or the like; Z is -CO-, etc. A is an aryl group, a heteroaryl group or the like], or a pharmaceutically acceptable salt thereof. [Effect] The compound (1) of the present invention and a pharmaceutically acceptable salt thereof are useful as a therapeutic drug for fibrosis by specifically acting on Edg-5. [Selection diagram] None
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2011087051-A1
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