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filingDate 2004-02-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_be4196cfeda6f5e8ceb95ffa99082560
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_29b9f49cad778cc0d970c1a152b3af06
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publicationDate 2006-08-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CO-5670352-A2
titleOfInvention ANILINIC PIPERIDINS REPLACED AS SELECTIVE ANTAGONISTS OF THE CONCENTRATION HORMONE OF MELANINA
abstract 1.- A compound having the structure where R1 is hydrogen, monofluoroalkyl, polyfluoroalkyl or straight or branched C1-C7 alkyl, aryl or heteroaryl, wherein the aryl or heteroaryl is optionally substituted with one or more of -F, -Cl, Br-, -I, -CN, -NO2, -CH3, CF3, -COCH3, -CO2R2, phenyl, phenoxy or straight or branched C1-C7 alkyl; wherein R2 is cyclopropyl or C3 alkyl -C4 straight or branched chain, wherein R3 is aryl or heteroaryl, wherein the aryl or heteroaryl is optionally substituted with one or more of F, -Cl, -Br, -I, -CN, -NO2, C1-alkyl -C7 straight or branched chain; where A is -H, -F, -Cl, -Br, -CN, -NO2, -COR3, -CO2R3, monofluoroalkyl, polyfluoralkyl or C1-C7 straight or branched chain alkyl ; wherein X is O or NH; yen wherein n is an integer from 0 to 5, inclusive. 2. The compound according to claim 1, wherein R1 is aryl optionally substituted with one or more of -F, -Cl, -Br, -I, -CN, -NO2, -COCH3, -CO2R2, or C1-C7 alkyl with straight chain; wherein R3 is phenyl; where A is H; and where X is O.
priorityDate 2001-07-05-04:00^^<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: 90.