Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_90a89ac945b13b12c19821f7d438e8d4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ccb9ef26f43ac2907a5b97404cb05707 |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P37-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P11-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P17-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K7-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00 |
classificationIPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P17-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P37-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P11-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-17 |
filingDate |
1988-08-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f844a2005ee1e35d36b13221925c27e3 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_06ce17d7a7698b799733ed9212cfb747 |
publicationDate |
1989-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
WO-8901780-A1 |
titleOfInvention |
Bradykinin antagonist peptides |
abstract |
The substitution of the L-Pro at the 7-position of the peptide hormone bradykinin or other substituted analogs of bradykinin with an aliphatic, cyclic or aromatic amino acid of the D-configuration converts bradykinin agonists into a bradykinin antagonist. The invention further includes additional modifications at other positions within the novel 7-position modified bradykinin antagonists including replacement of arginine in the one and nine positions and sequence deletions analogs and C-terminal and N-terminal extensions, which increase enzyme resistance, antagonist potency and/or specificity of the new bradykinin antagonists. The analogs produced are useful in treating conditions and diseases of the mammal and human body in which an excess of bradykinin or related kinins are produced or injected as by bites into the body. |
isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9713493-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11179424-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2739553-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6468972-B1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0334244-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0334244-A2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5416191-A |
priorityDate |
1987-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |