http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1207769-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8c646f75c4f7c6349f35c8fe01934921
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1f10e62b06b86a5b58dfc7dc134830d2
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P11-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-337
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-32
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4427
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-337
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-333
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-535
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P11-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-495
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-40
filingDate 1983-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1986-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0d7fba127c5572f546aff1136e70f226
publicationDate 1986-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1207769-A
titleOfInvention Pyrrolacetic amides having antiinflammatory activity
abstract "Pyrrolacetic amides having antiinflammatory acitivity" ABSTRACT OF THE DISCLOSURES N-monosubstituted and N,N-disubstituted amides of the 1-methyl-5-p-toluoylpyrrole-2-acetic acid, which are active as antiinflammatory, analgesic, antipyretic, antisecretive and antitussive agents, are disclosed. These amides are prepared by reacting an amine with an activated derivative of the 1-methyl-5-p-toluoylpyrrole-2--acetic acid of formula wherein X is an activating group suitable for promoting the formation of an amide bond.
priorityDate 1982-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID4498
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419485992
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID452902004
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397808
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9688
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425879072
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456171974
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393349
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448120584
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6101
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394811
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID10116
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453637368
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID179929
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14887622
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419493982
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID179929
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID402
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID452419213
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5509
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14284
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397310
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397365
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21886435
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID164963
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414865843
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID10116
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420280108
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559526
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70378573
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10942334
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419556970
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID85690582
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19840469
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420238519
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419524163
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419480928
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523291
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID947
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453876754
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID977
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18624872
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5733
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID4498
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID86740697
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453835784

Total number of triples: 74.