http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1668004-A1

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filingDate 2004-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a3e7ab6d4afe11906584bf23d8f82c40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_25414834850f86fb7385c52c0d3c3892
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d686427997392c7aad1f82c059659801
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_253c522ba48cf02951f5c4828e24a94c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_27d10e395e785eb799ef332fe5d635eb
publicationDate 2006-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1668004-A1
titleOfInvention Benzoxazole acetonitriles
abstract The present invention is related to benzoxazole acetonitriles as well as to pharmaceutical formulations containing such benzoxazole acetonitriles pof formula (I). Said benzoxazole acetonitriles are useful in the treatment of metabolic disorders mediated by insulin resistance or hyperglycernia, comprising diabetes type II, inadequate glucose tolerance, insulin resistance, obesity, polycystic ovary syndrome (PCOS). The present invention is furthermore related to methods of preparing benzoxazole acetonitriles (I). A is a pyrimidinyl.L is a secondary or tertiary amino group, or a 3-8 membered heterocycloalkyl, containing at least one heteroatom. selected from N, O, S or L is an acylarnino moiety.R1 is selected from the group comprising or consisting of hydrogen, sulfonyl, amino, CiC6-alkYl, C2-C6-alkenYl, C2-C6-alkynyl or Cl-C6-alkoxy, aryl, halogen, carboxy,aminocarbonyl, cyano or hydroxy.
priorityDate 2003-09-12-04:00^^<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: 1222.