http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BR-122014024864-B1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0a910d33c239980f3a705e312c5bad6a
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-12
filingDate 2001-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_03566b399ea1e7c596cdad5f937a6b2f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cfd1b21e15a782d73a99f8c1fff9f2e7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5581d5b4dda9f4bf3c3daa021a1b3a2d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_806aec21f9fa0c9ebaddc6a6f0aaddc5
publicationDate 2019-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-122014024864-B1
titleOfInvention PYRIMIDINE DERIVATIVE, PROCESS FOR PREPARING A PYRIMIDINE DERIVATIVE, PHARMACEUTICAL COMPOSITION, AND USE OF A PYRIMIDINE DERIVATIVE
abstract "Pyrimidine derivative, process for preparing a pyrimidine derivative, pharmaceutical composition, and use of a pyrimidine derivative" (i) the pyrimidine derivatives of formula (1) wherein q1, q2, ge R1 are as defined herein and their pharmaceutically acceptable salts and in vivo hydrolysable esters are described. The processes for their manufacture, pharmaceutical compositions and their use as cyclin-dependent serine / threonine kinase (cdk) and focal adhesion kinase (fak) inhibitors are also described.
priorityDate 2000-03-01-04:00^^<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: 421.