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filingDate 2015-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad1cc66eee4f9574537b3fb6b6784851
publicationDate 2016-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2016034946-A
titleOfInvention New prodrugs of steroidal CYP17 inhibitors / antiandrogens
abstract PROBLEM TO BE SOLVED: To provide a C-17-heterocyclic steroidal drug which is a prodrug having improved oral bioavailability and pharmacokinetics. A prodrug compound represented by Formula I. The compound is a useful inhibitor of the human CYP17 enzyme. (X is benzimidazole; Y is alkyl carboxyl having sulfonyl or phosphoric acid) [Selection] None
priorityDate 2009-02-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392451
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID36752
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID38841
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419547110
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419572553
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450796724
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID947
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID829894
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID34036
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID132971
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419528156
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID829895
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID829897
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9SWE3
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCV4HJ73
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Total number of triples: 455.