| Predicate |
Object |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-5325
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K1-061
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K1-062
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-3282 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-53
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-36 |
| filingDate |
2016-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate |
2021-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate |
2021-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
KR-102337328-B1 |
| titleOfInvention |
Systems and Methods for Synthesis of GAP Peptides in Solution Phase |
| abstract |
Disclosed are systems and methods for the synthesis of Fmoc/t Bu solution phase peptides, including the development of novel benzyl-type GAP protecting groups, and uses related thereto. This novel GAP protecting group is used instead of a polymeric support to facilitate C to N Fmoc peptide synthesis without chromatography, recrystallization or polymeric support. GAP groups can be added and removed in high yield. |
| priorityDate |
2015-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |