http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5461128-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c999fee6428152a996011d506925c2d7 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C279-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C239-00 |
| filingDate | 1977-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81197e4db86bb0de1fdedd8421028718 |
| publicationDate | 1979-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-S5461128-A |
| titleOfInvention | Peptide derivative |
| abstract | NEW MATERIAL:Peptide derivative of formula and its acid addition salt (R is serylglycyl, leucylglycyl, glutarylglycyl, tert-alkyloxycarbonylglycyl, valylprolyl or ter-alkyloxycarbonylprolyl). n EXAMPLE: t-Butyloxycarbonyl-glycyl-L-arginine-p-nitroanilide derivative. n USE: Useful as a synthetic substrate having specificity to enzymes such as trpsin, kallikrein, thrombin, urokinase, etc. n PROCESS: The title compound of formula is prepared e.g. by reacting L-arginine- p-nitroanilide di-hydrochloride with t-butyloxycarbonylglycine-N-hydroxysuccinimide ester in a solvent, followed by eliminating the amino- or OH-protecting groups. n COPYRIGHT: (C)1979,JPO&Japio |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6061557-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6332348-B2 |
| priorityDate | 1977-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 48.