http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2018071290-A1

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filingDate 2016-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_28d27f303d85f7d17f51cb78c4db16e1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2d8c51f3041f325365a8c223b12fc504
publicationDate 2018-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2018071290-A1
titleOfInvention Solid Pharmaceutical Formulation of PARP Inhibitors and Use Thereof
abstract The present invention provides a solid pharmaceutical formulation of PARP inhibitors and its use thereof, and more specifically a solid dispersion powder including 5-fluoro-1-(4-fluoro-3-(4-(pyrimidin-2-yl)piperazine-1-carbonyl)benzyl)quinazoline-2,4(1H,3H)-dione and polymers, wherein the content of polymers is from about 50 wt % to about 80 wt %, and wherein less than 10 wt % of 5-fluoro-1-(4-fluoro-3-(4-(pyrimidin-2-yl)piperazine-1-carbonyl)benzyl)quinazoline-2,4(1H,3H)-dione is in crystalline form. The present invention also provides a method for preparing the solid dispersion powder, a pharmaceutical composition including the solid dispersion powder and the use of the pharmaceutical composition for treating diseases caused by PARP activity abnormalities.
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226408603
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5329102
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID3355109
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559251
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226395671
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419492167
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP54107
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226395672
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448969875
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP04931
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Total number of triples: 395.