http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2001505578-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K5-06078 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-065 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-04 |
| filingDate | 1997-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2001-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2001505578-A |
| titleOfInvention | Peptide synthesis using sulfonyl protecting groups |
| abstract | (57) [Summary]nMethods and compositions for synthesizing peptides having a sulfonyl protecting group are provided. In this method, an amino acid having α-amino protected by a sulfonyl group is contacted with a second amino acid monomer unit under conjugation conditions so that the protected amino acid and the second amino acid monomer unit can be combined by a peptide bond. The contacting step can be repeated one more time to obtain a peptide of the desired length. Also provided are methods of regiospecific modification using the present sulfonyl protecting groups. The method is particularly useful for solid phase peptide synthesis. |
| priorityDate | 1996-12-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 109.