http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H10147598-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8af19d05c71d306141bc1fdbd2f05f39 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-585 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-575 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-23 |
| filingDate | 1996-11-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4ef278408ff9f918bafcf50bc0ea752f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5f68090110f7ef991d362ff447e7ff6a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae7e9e0faf3b67e7faa8982cfde5c37a |
| publicationDate | 1998-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H10147598-A |
| titleOfInvention | Glycosyl calcitonin derivatives, their preparation and intermediates |
| abstract | (57) [Summary] (Modified) [Problem] Not only can the activity and function of calcitonin be improved, but it can also be used as a raw material for the synthesis of calcitonin having a long natural sugar chain utilizing the sugar chain transfer reaction of endoglycosidase. Provided is a derivative in which N-acetylglucosamine is glycosylated on calcitonin and a technique for producing the same. Kind Code: A1 N-acetylglucosamine is added to the nitrogen atom of the side chain amide group of the asparagine residue at the 3-position of eel calcitonin. A glycosyl calcitonin derivative represented by the following formula, wherein (GlcNAc) is glycosylated, and a method for producing the same. And an intermediate represented by the following formula. (In the formula, Acm represents an acetamidomethyl group.) |
| priorityDate | 1996-11-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 81.