http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1646385-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6e29526f284c0155fd79806c9dd5a1c7
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-4535
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4535
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K-
filingDate 2004-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_19b6d8c562c52cd4c9e0946214ed866c
publicationDate 2006-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1646385-A2
titleOfInvention Use of benzothiopenes to treat and prevent prostate cancer
abstract Disclosed herein is a method for treating and preventing prostate cancer, and particularly androgen-independent prostate cancer, the method including administering to a mammal a benzothiopene having Formula (I) or pharmaceutically acceptable salts or prodrugs thereof, wherein R and R1, are each independently selected from the group consisting of hydrogen, -COR2, -COR3, and R4; R2 is selected from the group consisting of hydrogen, C1-C14 alkyl, C1-C3 chloroalkyl, C1-C3 fluoroalkyl, C5-C7 cycloalkyl, C1-C4 alkoxy, and phenyl; R3 is phenyl with at least one substitution selected from the group consisting of C1-C4 alkyl, C1-C4 alkoxy, hydroxy, nitro, chloro, fluoro, trichloromethyl, and trifluoromethyl; R4 is selected from the group consisting of C1-C4 alkyl, C5-C7 cycloalkyl, and benzyl; and R5 is selected from the group consisting of oxygen and -C=O. The method may further include the administration of an estrogen lowering drug to enhance efficacy of the compound of the present invention.
priorityDate 2003-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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