http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112608376-B
Outgoing Links
Predicate | Object |
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classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K47-542 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-57563 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-575 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-107 |
filingDate | 2020-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2022-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2022-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-112608376-B |
titleOfInvention | Preparation method of active peptide Apelin |
abstract | The invention relates to a preparation method of an active peptide Apelin, which comprises the step of connecting 2- (4-chlorphenyl) -2, 2-difluoroacetic acid by a solid phase synthesis method after the Apelin is prepared by the solid phase synthesis method. The active peptide Apelin (2- (4-chlorphenyl) -2, 2-difluoroacetic acid-QRPRLSHKGPMPF) is obtained by a solid phase synthesis method, and the activity of the active peptide Apelin obtained based on the method can be further improved while the half-life period is prolonged. |
priorityDate | 2020-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 65.