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filingDate 1998-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9c7a40e445c36d721e897978b9c5b930
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8d21329ff0d03e7f705912a334336643
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad4ef552f203773f53582ba1f8b0eb45
publicationDate 1999-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0895989-A1
titleOfInvention 1-[4-(Substituted alkoxy)benzyl] naphthalene compounds having estrogen inhibitory activity
abstract A class of substituted benzylnaphthylene compounds ofnthe structuren nwhere R 1 and R 2 are independently hydrogen, alkyl of one tonsix carbon atoms, acyl of two to six carbon atoms, ornphenacyl; X is -(CH 2 ) 1-6 ; Y is absent or is selected fromn1,4-piperazinylene; ureido; N-(lower alkyl)ureido; N'-(lowernalkyl)ureido; or N, N'-(di-lower alkyl ureido; and Z is 1-,n2- or 3-pyrrolidinyl; 1-, 2-, or 3-[1-(lower alkyl)npyrrolidinyl]; 1- 2-,3- or 4-piperidinyl; 1-, 2-, 3- or 4-[1-lowernalkyl)piperidinyl]; N,N-dialkyl; 1-azepinyl; 1- orn2-naphthylamino, 4-morpholinyl, dimethyl-4-morpholinyl, 3-azaspiro[5.5]undecan-3-yl;npyrrolidinon-1-yl; unsubstitutednphenyl; or phenyl substituted with acyl of two to fourncarbon atoms, alkyl of one to four carbon atoms, halo, ornalkoxy of one to four carbon atoms; with the proviso that nnis not 2 or 3 when Z is 1-pyrrolidinyl, 1-piperidinyl, 1-azepinyl,n4-morpholinyl, N,N-dimethylamino or N,N-diethylamino;nare selective estrogen receptor modulators useful innthe prophylaxis or treatment of breast cancer.
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type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393946
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231889027
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413551482

Total number of triples: 918.