| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1fd3686cb239172b74cee63622184c3c |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-575
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K17-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P37-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K1-065
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P37-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-57581
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-575
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K17-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00 |
| filingDate |
2007-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate |
2013-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4b771b4cddccbb9135c4d6f5feca5dc1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_718467672ea8b2a0b1179f8f4c42b10a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8540657092542189b547c1ff0e783336
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3526bcfe35d0c86df323e8c9c0e805c8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_93832438fcf4fd387b94f12b0e74e0db |
| publicationDate |
2013-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
ES-2399248-T3 |
| titleOfInvention |
Procedure to synthesize thymosins |
| abstract |
Method for obtaining thymosins and / or their pharmaceutically acceptable salts by solid phase synthesis polymeric supports comprising the steps of linearly synthesizing timus derived peptides in solid phase, incorporating less a Thr or Ser in the form of a pseudoproline dipeptide in the sequence, obtain the thymosins by treating peptidyl resin with trifluoroacetic acid, and purify the thymosins by RP-HPLC. The present invention also protects the isolated and / or purified compound obtained by said process as well as the use thereof in the preparation of a medicament. |
| priorityDate |
2006-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |