http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2300459-A1

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filingDate 2009-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_501c03b376f4e0c3455252cc8d14500d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0031c3cf658ced508259c5520918d577
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ed8146c9bd729a6e19c02b9ad0560855
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_380f0c2123a1a216aa565951be3f3b46
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_83a7246c161cc7884bc28742c67e3807
publicationDate 2011-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2300459-A1
titleOfInvention Novel phenylpyrazinones as kinase inhibitors
abstract The present invention provides 5 -phenyl- 1H-pyrazin-2 -one derivatives according to generic Formulae I-V: wherein, variables Q, R, Y 1 , Y 2 , Y 2' , Y 3 , Y 4 , n and m are defined as described herein, which inhibit Btk. The compounds disclosed herein are useful to modulate the activity of Btk and treat diseases associated with excessive Btk activity. The compounds are further useful to treat inflammatory and auto immune diseases associated with aberrant B-cell proliferation such as rheumatoid arthritis. Also disclosed are compositions comprising compounds of Formulae I-V and at least one carrier, diluent or excipient.
priorityDate 2008-07-02-04:00^^<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: 1246.