| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_84d9adaa7e7ce01ce8020f5c721aba10 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K7-23
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P5-00 |
| classificationIPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-23
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P5-00 |
| filingDate |
1993-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate |
1997-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fa5cf9dbd452976f1961b03662351466
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7e5cd071e44e54cf2118cb00cd65dc24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_791ec4791dbc665b6ba1fc53c58c553b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_760eb25676e99d395248a5cd9e25546b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b2158644b6634be4261eca5247893d4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_715b160fae0b8a12e479f387cbb0dbfd |
| publicationDate |
1997-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
US-5698522-A |
| titleOfInvention |
6-position modified decapeptide LHRH antagonists |
| abstract |
PCT No. PCT/US93/11628 Sec. 371 Date Jun. 1, 1995 Sec. 102(e) Date Jun. 1, 1995 PCT Filed Nov. 30, 1993 PCT Pub. No. WO94/13313 PCT Pub. Date Jun. 23, 1994The present invention provides a class of decapeptide compounds which are potent antagonists of LHRH activity and which have the structure A1-D2-E3-G4-J5-L6-M7-Q8-R9-T10. The compounds of the percent invention are characterized by having an OMEGA -amino-functionalized side chain on the D-aminoacyl residue at position 6. The OMEGA -amino group of this side chain is further derivatized by the attachment of an extending group which likewise has a terminal amino group which is capped by an acyl group. |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6395559-B1 |
| priorityDate |
1992-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |