| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_204ea9f0f83d1c51a916e46a41a6a14a |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-99
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00 |
| filingDate |
2002-08-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_34ff06b4aadccd8fb7b6981b877754fb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eca4c733dda805b6e3e41d00aed653d1 |
| publicationDate |
2004-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
JP-2004083427-A |
| titleOfInvention |
Cyclic hexapeptide and proteasome inhibitor |
| abstract |
An object of the present invention is to provide a novel cyclic hexapeptide having a proteasome inhibitory activity. Kind Code: A1 A novel cyclic hexapeptide having a structure of cyclo (-X-phenylalanyl-prolyl-X-phenylalanyl-prolyl) was synthesized and found to exhibit proteasome inhibitory activity. X represents an α-amino acid residue, whose side chain functional group may be protected or modified. |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008518622-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-116162135-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113150077-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-116162135-A |
| priorityDate |
2002-08-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |