http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9139565-B2

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filingDate 2011-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5f8ce102535ead17d965b9b56ad1fa88
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_893b8388d6d9454456d363ea13b17abb
publicationDate 2015-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-9139565-B2
titleOfInvention Histone deacetylase (HDAC) inhibitors targeting prostate tumors and methods of making and using thereof
abstract Compounds of Formula (I), and methods of making and using thereof, are described herein; wherein AR is an aryl group, ZBG is a Zinc Binding Group, and other substituents are as defined herein. The compounds can be administered as a pharmaceutically acceptable salt, prodrug, or solvate. The compounds may be useful to treat and/or prevent hyperproliferative disorders which may include hormone sensitive and hormone refractory prostate cancers. The compounds can be formulated with a pharmaceutically acceptable carrier and, optionally one or more pharmaceutically acceptable excipients, for enteral or parenteral administration.
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type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 1412.