http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5762246-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e45efeaa6a34dfd9d44fa29a7fe0c806 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-575 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-16 |
| filingDate | 1980-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9d6b248fef55bf43572fc2fd685eb69a |
| publicationDate | 1982-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-S5762246-A |
| titleOfInvention | Cyclic pentapeptide derivative |
| abstract | NEW MATERIAL:The compound of formulaI(R is H, benzyl or tert-butyl; R 1 is lower alkyl; Tyr is L-tryosine; Ile is L-isoleucine; Gln is L-glutamine; Asn is L-asparagine; Asu is L-aminosuberic acid). n EXAMPLE: The compound of formula II. n USE: Synthetic intermediate for an oxytocic. Extremely useful for the preparation of cargtosin for formula III which is a derivative of oxytosin. n PROCESS: The compound of formulaIis prepared by condensing the compound of formula IV (Bu t is tert-butyl; Z is benzyloxycarbonyl) (starting material) successively with desired peptides or amino acids, and cyclizing the product. n COPYRIGHT: (C)1982,JPO&Japio |
| priorityDate | 1980-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 34.