| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_07c9542186133097bd6bbb7d92393090 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K5-06078
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K1-063
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K1-064
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D285-125
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-12 |
| classificationIPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-12 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-065
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-125
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-06 |
| filingDate |
1996-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate |
1999-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_832cd6be92ed2a6b422ad99a965d4912
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_36a2c3a62fa0029ce7ffc3b418814d9f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c8dd1dfccdb69f5c7438664b274b80f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1505820c97f115d75a9400c1dfa7a31d |
| publicationDate |
1999-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
US-5900427-A |
| titleOfInvention |
N-heteroarenesulfonyl-protected amino acid reagents for peptide synthesis |
| abstract |
This invention relates to the use of heteroarenesulfonyl groups as protecting groups for amino groups, particularly the amino groups of amino acids, and specifically to nitrogen-protected (N-protected) amino acid reagents, which are particularly well-suited for use in peptide syntheses. In particular, the N-protected amino acid reagent is an N-heteroarenesulfonyl-protected amino acid halide. The heteroarenesulfonyl protecting groups are readily removed under relatively mild conditions. |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2003139379-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6207698-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6235768-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0125257-A2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6441021-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0125257-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6881727-B2 |
| priorityDate |
1996-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |