http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-8304923-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_39ae96c0ecc22ff90ff986371a3cea0f
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K5-0215
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P37-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C237-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C237-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C237-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P37-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-22
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/C07C271-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K5-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-195
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-27
filingDate 1981-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1983-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-8304923-A1
titleOfInvention A PROCEDURE FOR THE PREPARATION OF A PEPTIDE.
abstract PROCEDURE FOR OBTAINING PEPTIDES AND THEIR PHYSIOLOGICALLY COMPATIBLE SALTS, OF FORMULA (I), IN WHICH R, R, R, R AND R MAY BE SEVERAL TYPES OF RADICALS. IT CONSISTS OF THE REACTION OF A COMPOUND OF FORMULA (II), OR A SALT OF THE SAME, WITH A COMPOUND OF FORMULA (III) OR A SALT OF THE SAME, IN WHICH R <A IS ALCANOYL OR ARALKANOYL; R <A IS PROTECTED CARBOXI; R <A IS AMINO PROTECTOR GROUP; AND R 3 AND R HAVE THE SAME MEANING AS IN FORMULA (I); FOLLOWED BY THE ELIMINATION REACTION OF THE PROTECTIVE GROUPS. THE FORMATION REACTION OF THE PEPTIDIC BOND IS EFFECTED IN AN INERT SOLVENT, IN THE PRESENCE OF A CONDENSING AGENT, UNDER ANHYDROUS CONDITIONS, AT A TEMPERATURE -20 C AND THE AMBIENT. THESE COMPOUNDS HAVE PHARMACOLOGICAL APPLICATIONS FOR THEIR ANTITUMORAL ACTIVITY AND AS INTERMEDIATES FOR THE SYNTHESIS OF OTHER COMPOUNDS WITH BIOLOGICAL ACTIVITY.
priorityDate 1980-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID783
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397365
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425193155
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458396411

Total number of triples: 32.