http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008266349-A

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filingDate 2008-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7dacfd78beb75b8005baf765f1c1b6b2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3ae9ac82bfda58064eee2e59a495973f
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d24e7984a7bb73b341d1ad1858a98e4e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a5bb5756902ddd7673f859606c7bd4ad
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2a27a766c20889bda43b19a490b6d5f4
publicationDate 2008-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2008266349-A
titleOfInvention Substituted thiazole derivatives having a 3-pyridyl group, method for producing the same, and use thereof
abstract The present invention provides a pharmaceutical composition having a steroid C 17,20 lyase inhibitory activity and useful as a preventive / therapeutic agent for tumors such as prostate disease and breast cancer. SOLUTION: Formula: (In the formula, A 1 represents an optionally substituted aromatic hydrocarbon group or an optionally substituted heterocyclic group, one of A 2 and A 3 is a hydrogen atom, a halogen atom, A C 1-4 aliphatic hydrocarbon group which may have a substituent or a carboxyl group which may be esterified, an aromatic carbon which the other of A 2 and A 3 may have a substituent A hydrogen group or an optionally substituted heterocyclic group is shown, but at least one of A 1 , A 2 and A 3 is an optionally substituted 3-pyridyl group). A steroid C 17,20 lyase inhibitor comprising the compound represented by the formula: [Selection figure] None
priorityDate 2000-12-08-04:00^^<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: 1044.