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filingDate 1998-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2003-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8d21329ff0d03e7f705912a334336643
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a05191de83622f46c1551290d7d0d41b
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publicationDate 2003-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6509356-B1
titleOfInvention 1-(4-(Substituted alkoxy)benzyl)naphthalene compounds having estrogen inhibitory activity
abstract A class of substituted benzylnaphthylene compounds of the structurewhere R1 and R2 are independently hydrogen, alkyl of one to six carbon atoms, acyl of two to six carbon atoms, or phenacyl; X is -(CH2)1-6; Y is absent or is selected from 1,4-piperazinylene; ureido; N-(lower alkyl)ureido; N'-(lower alkyl)ureido; or N, N'-(di-lower alkyl ureido; and Z is 1-, 2- or 3-pyrrolidinyl; 1-, 2-, or 3-[1-(lower alkyl) pyrrolidinyl]; 1- 2-, 3- or 4-piperidinyl; 1-, 2-, 3- or 4-[1-lower alkyl)piperidinyl]; N,N-dialkyl; 1-azepinyl; 1- or 2-naphthylamino, 4-morpholinyl, dimethyl-4-morpholinyl, 3-azaspiro[5.5]undecan-3-yl; pyrrolidinon-1-yl; unsubstituted phenyl; or phenyl substituted with acyl of two to four carbon atoms, alkyl of one to four carbon atoms, halo, or alkoxy of one to four carbon atoms; with the proviso that n is not 2 or 3 when Z is 1-pyrrolidinyl, 1-piperidinyl, 1-azepinyl, 4-morpholinyl, N,N-dimethylamino or N,N-diethylamino; are selective estrogen receptor modulators useful in the prophylaxis or treatment of breast cancer.
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23555636
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18675919
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231888450
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12020303
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23555635
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID91547831
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18675918
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5460308
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226396344
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID160350948
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2244
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231888449
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID140025927
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18675925
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID136191117
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231888336
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID140025926
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID243467952
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18675924
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226395599
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421757444
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID243457401
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID140025925
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23555640
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18675923
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID136230068
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23555639
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18675922
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID140025931
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23555638
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18675929
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID140025930
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23555637
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18675928
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226394094
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID142295813
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID243508589
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID140025929
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID245465799
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458395906

Total number of triples: 1268.