http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104003939-B

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Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D235-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P13-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4184
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
filingDate 2014-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2017-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-104003939-B
titleOfInvention Diaryl substitution thiohydantoin class compound and preparation method and application
abstract The invention discloses diaryl substitution thiohydantoin class compound, structure is as shown in logical formula (I): Wherein, R 1 It is hydrogen, halogen or trifluoromethyl;R 2 It is hydrogen, halogen, trifluoromethyl, itrile group or alkoxy;R 3 It is hydrogen, halogen or itrile group;R 4 It is hydrogen or halogen;R 5 It is hydrogen, halogen, methyl, N methylcarbamoyls, N ethyls amine formyl, N isopropylamines formoxyl, N cyclopropylamine formoxyls.Diaryl substitution thiohydantoin class compound, especially 7b 7g of the invention, 7i 7k, 7m 7p, 7r 7t have stronger GIA, can be used for preparing antineoplastic to hormone-independent prostate cancer cell LNCaP.
priorityDate 2014-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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