http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20150056853-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-10
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
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filingDate 2013-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d750997c44c1af2c4a08e89919217119
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3df7bb38f7508eb45c7607e241b1a2fe
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_46e3bb68d03bfa1ce04442b196b5bd65
publicationDate 2015-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20150056853-A
titleOfInvention Use of a tetrasubstituted pyrazolo[4,3-d]pyrimidine compound for treating diabetic nephropathy
abstract The present invention relates to a process for the preparation of 1- (2-ethoxyethyl) -5- (ethyl (methyl) amino) -7- (4-methylpyridin- (ESRD) in a patient, comprising administering to the patient a therapeutically effective amount of at least one compound selected from the group consisting of: &lt; RTI ID = 0.0 &gt; [4, 3-d] pyrimidine-3-carboxamide. The invention also includes administration of a pharmaceutical composition to delay progression to ESRD. - (4-methylpyridin-2-yl) amino) -N- (methylsulfonyl) -lH-pyrazolo [4 , 3-d] pyrimidine-3-carboxamide
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2015202576-A1
priorityDate 2012-10-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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