Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6d5d77f66f59d53a3906f98ab95a55ef |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-70571 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-57423 |
classificationIPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-91 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-705 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-53 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K16-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-574 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-005 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K39-395 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-577 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-195 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K49-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K16-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00 |
filingDate |
1998-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a936024a7e99e687679907e4b232bf4b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_25a1139c53769edd8a7fafb368de83a6 |
publicationDate |
1999-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
JP-H1171298-A |
titleOfInvention |
Pharmaceutical and diagnostic compositions containing neuropeptide antagonists |
abstract |
(57) [Summary] (Modified) [PROBLEMS] To provide a method of using a neuropeptide antagonist. SOLUTION: The polypeptide having the features of 1) to 6). 1) A single-chain glycopolypeptide rich in mannose side chains. 2) Selective binding to bombesyl-type polypeptide. 3) molecular weight 75-85 kDa. 4) Isoelectric point 6.4-6.9. 5) The molecular weight of the core protein obtained using endo-β-N-glucosaminidase from Flavobacterium meningosepticum is about 42 Kd. 6) 3-15 mM, preferably 5-10 mM Mg ++ The equilibrium dissociation constant at 15 ° C. was 1.9 × 10 −10 M by kinetic analysis using a membrane preparation obtained by disrupting Swiss 3T3 cells in an aqueous medium containing 2.1 × 10 −10 M by coupling). |
priorityDate |
1988-03-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |