http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2019006680-A

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filingDate 2015-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2977e337327aa63dbacd5f8d760f3357
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0e67b5e703b10f74a5b733f8b9cae541
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_39cbb6756b5059959680e4f6468695e5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_89fcb195102cd86551f3fe98f5b74b19
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e3052e06e3704321c60590f3343a7dcf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1bd343bb7068fba789bd608622e5bafe
publicationDate 2019-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2019006680-A
titleOfInvention Pyrazolopyridine derivatives and uses thereof
abstract The present invention provides a novel peroxome proliferator-activated receptor (PPARα) transcription activator useful for the treatment of dyslipidemia and the like. A 1H-pyrazolo [3,4-b] pyridine derivative represented by the formula (1) is provided. [R1 is H, halogen, alkyl, halogenated alkyl, alkoxy, unsubstituted / substituted phenyl, unsubstituted / substituted phenoxy or unsubstituted / substituted benzyloxy; R2 is a linear / branched alkyl group or cyclic alkyl R3 is linear / branched alkyl; R4 is carboxy, ethoxycarbonyl or a propionic acid group having alkyl in the linear / branched α-position; X is C or N] [Selection] None
priorityDate 2015-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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