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filingDate 2003-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2008-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a50a2dbaecf6697dd511cc0b5da0485a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e649447a2196f504909067399d64b65c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_97fca1051e817db19ca4f12142f9eed1
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publicationDate 2008-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7453010-B2
titleOfInvention Phenylcyclohexylpropanolamine derivatives, preparation and therapeutic application thereof
abstract The invention relates to compounds of general formula (I): n n n n n n n n n n n n where R 1 represents H or a (C 1 -C 4 )alkyl, —CO(C 1 -C 4 )alkyl, (C 1 -C 4 )alkylphenyl or —CO-phenyl group, said phenyl optionally being substituted; R 2 represents H, a halogen atom, an —S(O) z (C 1 -C 4 )alkyl group, where z is equal to 0, 1 or 2, an —NHSO 2 (C 1 -C 4 )alkyl group, an —NHSO 2 -phenyl group or an —NHSO 2 —(C 1 -C 4 )alkylphenyl group, said phenyl optionally being substituted; R 3 represents an —X—R 4 group—in which X represents a bond, an oxygen atom or a —CH 2 — group and R 4 represents H or a —CR 5 R 6 —COOR 7 group, where R 5 , R 6 and R 7 independently represent H or a (C 1 -C 4 )alkyl group—a phenyl group optionally substituted or fused with a dioxolane group, a —CO—NR 8 R 9 group—where R 8 represents H, a (C 1 -C 4 )alkyl group or a (C 1 -C 4 )alkyl(C 1 -C 4 )alkoxy group and R 9 represents a (C 1 -C 4 )alkyl(C 1 -C 4 )alkoxy group, a —(CH 2 ) n -A group, where n is equal to 0, 1, 2, 3 or 4 and where A represents an indolyl group, a fluorenyl group or a phenyl group which is substituted, an optionally substituted —NH-phenyl group or a —CH(R 10 )—(CH 2 ) n —COOR 11 group, where n is 0, 1, 2 or 3 and where R 11 represents H or a (C 1 -C 4 )alkyl group and R 10 represents H, a (C 1 -C 4 )alkyl group or a —CH 2 -phenyl group, said phenyl optionally being substituted, or a —COOR 12 group, where R 12 represents H or a (C 1 -C 4 )alkyl group; their process of preparation and their therapeutic application.
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID87485096
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129284402
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393439
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448509792
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419538880
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID142091473
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67749
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9900389
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID455295402
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129625286
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID223960549
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID142016773
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID455295166

Total number of triples: 611.