| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3e9445e5e3626f36e932c6451a928250 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S930-16 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K1-107
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K1-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-6555 |
| classificationIPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-113
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-107
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-655
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-575 |
| filingDate |
1980-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate |
1981-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
ES-8200861-A1 |
| titleOfInvention |
PROCEDURE FOR OBTAINING ACILPEPTIDES |
| abstract |
PROCEDURE FOR THE OBTAINING OF ACILPEPTIDES DERIVED FROM SOMATOSTATIN AND ITS ANALOGUES, AS WELL AS NON-TOXIC SALTS AND USABLE PHARMACOLOGICALLY COMPLEXES OF THEM. IT CONSISTS OF REACTING A PEPTIDE WITH AN ALCANCARBOXYL ACID WITH A MAXIMUM OF 18 CARBON ATOMS, OR WITH A REACTIVE DERIVATIVE OF AN A-AMINO ACID, IN WHICH THE AMINO GROUPS ARE PRESENTED IN A PROTECTED FORM AND THE PROTECTIVE GROUPS IN THE DISASSEMBLE . ACILPEPTIDES CAN ALSO BE OBTAINED BY CYCLING A LINEAR PEPTIDE. NON-TOXIC ADDITION SALTS ARE OBTAINED BY TREATING ACILPEPTIDES WITH ORGANIC OR INORGANIC ACIDS. THE ACILPEPTIDES MAY BE PRESENT IN THE FORM OF COMPLEXES, WITH A STRUCTURE NOT FULLY DEFINED, WHICH ARE FORMED BY ADDING CERTAIN ORGANIC OR INORGANIC SUBSTANCES TO THE PEPTIDES. THE PROCESS OFFERS MULTIPLE VARIANTS. FOR USE IN THE OBTAINING OF PREPARATIONS FOR THERAPEUTIC PURPOSES, ESPECIALLY FOR THE TREATMENT OF FUNCTIONAL DISTURBANCES IN WHICH THE SECRETION OF THE GROWTH HORONE OR GLUCAGONE IS HIGHER THAN NORMAL. |
| priorityDate |
1979-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |