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filingDate 1991-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1999-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_408de7bd1523db347887b0b3f7cbf625
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_318cafdfefb46f2b3b3e3db968fbb431
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ec6d8e6d7127ee32d5efa7675870a20a
publicationDate 1999-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0743302-B1
titleOfInvention Sulfonamide fibrinogen receptor antagonists
abstract Sulphonamido-phenylalkanoic acid derivs. of formula (I), and their salts, are new. In (I), R1 = Het1 opt. substd. NR6R7, R6R7NC- (=NR6)- R6R7NC(=NR6)NH-, R6C(=NR7)NR7- or a gp. (a) or (b); Het1 = a 4-8 member heterocyclic ring contg. 1-4 heteroatoms from N, O, S; R6, R7 = H, 0-10C alkyl or cycloalkyl, both opt. substd. Het2 = 1-4C alkanoylamino, 1-6C alkoxycarbonyl, 0-6C alkylamino; 1-10C alkylsulphonylamino, 4-10C aralkylsulphonylamino, 4-10C aralkyl, 1-10 1-10C alkaryl, 1-10C alkylthio 4-10C aralkylthio, 1-10C alkylsulphinyl, 4-10C aralkylsulphinyl, 1-10C alkylsulphonyl, 4-10C aralkylsulphonyl, aminosulphonyl, 1-10C alkylaminosulphonyl, 4-10C aralkylsulphonylamino, oxo, thio, or 1- or 2-ethenyl or 3- propenyl, all opt. substd.; "alkyl" = from alkane, alkene or alkyne; alkoxy = O-alkyl; aralkyl and alkaryl contain alkyl as defined above and aryl defined below; Het2 = a 5 or 6 membered satd. heterocyclic ring contg. 1-4 heteroatoms from N, O, S; aryl = a mono- or poly-cyclic ring system of 5- and 6-membered aromatic rings contg. 0-4 heteroatoms from N, O, S; R2, R3 = H, aryl, or 0-10C alkyl or cycloalkyl both opt. substd.; R4 = aryl, 1-10C alkyl or cycloalkyl, 4-1UC aralkyl, 1-10C alkoxyalkyl, 1-10C alkaryl, 1-10C alkylthioalkyl, 1-10C alkoxythioalkyl, 1-10C alkylamino, 4-10C aralkylamino, 1-10C alkanoylamino, 4-10C aralkanoylamino, 1-10C alkanoyl, 4-10C aralkanoyl, or 1-10C carboxyalkyl opt. substd. R5 = Het1, COR8, or CSR8; R8 = e.g. OH, 1-10C alkyloxy, 1-10C alkaryloxy, etc. X. Y, Z are opt. substits. and = NR6, O, S, SO, CO, CS CH(OH), SO2, CR6=CR7, CC, Het1, (opt. substd. at any atom with R6), aryl, CONR6, NR6CO, NR6SO2, or SO2NR6; m = 0-10; n = 0-10; and p = 0-3.
priorityDate 1990-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID45051774
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID243
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID136172803
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID135730987
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226395791
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70044577
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID16790
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226396432
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54678486
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129713953
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226399944
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226397116
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127955030
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID229667635
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129129286
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10219638
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226397117
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID227291695
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID134392895
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57260454
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70045189
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10446560
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70047165
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID453
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128165861
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID16211742
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70044691
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6251
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID87059622
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6335613
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID16211353
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID159357
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393970
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11177
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID232908344
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129568515
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393971
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70044694
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID522596
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70042853
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226394558
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID518472
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7371
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID61054
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID232916827
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID517055
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128707670
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19348031
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID232916833
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393245
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57158132
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7799
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7107
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13950370
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127835182
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19348032
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11724
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23665730
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226397856
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15793
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226394110
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID135832627

Total number of triples: 334.