http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0719253-B1

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filingDate 1994-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2004-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f289ca091dea91e03fa5cfc160c32fdf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_93e1e3f0e02fc2944591c6400f019701
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d7a34dec93d03273037e5c7ff537bcf9
publicationDate 2004-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0719253-B1
titleOfInvention 3-amino-5-carboxy-substituted piperidines and 3-amino-4-carboxy-substituted pyrrolidines as tachykinin antagonists
abstract A compound of the chemical formula (I) and its pharmaceutically acceptable salt, wherein Y is C2-C4 alkylene; Z is a valence bond or C1-C6 alkylene; R<1> is substituted or unsubstituted aryl (e.g., phenyl and naphthyl) or heteroaryl (e.g., thienyl and furyl); R<2> is hydrogen or C1-C6 alkyl; R<3> is hydrogen, hydroxy or the like; R<4> is substituted or unsubstituted benzyl or the like. Typical examples are (2S*,3S*,4S*,5R*)-4-Carboxy-3-[N-(5-Isopropyl-2-methoxy-benzyl)amino]-5-methyl-2-phenylpyrrolidine and (2S*,3S*,5S*)-5-Carboxy-3-[N-(2-methoxy-5-trifluoromethoxybenzyl)amino]-2-phenylpiperidine. The novel substituted azaheterocyclecarboxylic acids in this invention have excellent substance P antagonistic activity and are thus useful for the treatement of gastrointestinal disorders, central nervous system disorders, allergy, inflammatory diseases, asthma, pain, emesis or migraine in mammals, especially humans.
priorityDate 1993-09-17-04:00^^<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/substance/SID245099657
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69936688
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54001762
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID135752319
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226394201
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393570
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57116319
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69822724
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID136076275
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID56988295
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127996738
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57262255
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6775
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10387
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15454929
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69902804
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID135808272
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15454928
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID56974186
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129945642
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID53663914
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127780464

Total number of triples: 319.