http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6967212-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-14
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-14
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-14
filingDate 2002-11-14^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2005-11-22^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c801cc2003c37f445802e07788db7747
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dbc24e1331210a1964ea9c03a673c620
publicationDate 2005-11-22^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6967212-B2
titleOfInvention Substituted azole acid derivatives useful as antidiabetic and antiobesity agents and method
abstract Compounds are provided which have the structure n n nwherein Q is C or N; R 2a , R 2b , R 2c , X 1 to X 7 , R 1 , R 2 , R 3 , R 3a , R 4 , A, Y, m, and n are as defined herein, which compounds are useful as antidiabetic, hypolipidemic, and antiobesity agents. The present invention further provides a method for treating obesity and dyslipidemia in mammals including humans through simultaneous inhibition of peroxisome proliferator activated receptor-γ (PPARγ) and stimulation of peroxisome proliferator activated receptor-α (PPARα).
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priorityDate 2001-05-30^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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