http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2524878-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d709e3167fa2f99a1803c9cfeb0aca63 |
| 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/C07K14-57509 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-23 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K7-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-575 |
| filingDate | 1983-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_291ec7205453ee564916f058757271b4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3098f34d726b1eb9eadbc9d35ad9da8c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fe5827a4cae976321430e6eafa8bce91 |
| publicationDate | 1983-10-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | FR-2524878-A1 |
| titleOfInvention | PEPTIDES WITH BIOLOGICAL ACTIVITY AND MEDICINE CONTAINING THEM |
| abstract | PEPTIDE WITH BIOLOGICAL ACTIVITY AND THE MEDICINAL PRODUCT CONTAINING THEM. THESE PEPTIDES HAVE THE FORMULA: XA-PRO-PRO-ILE-SER-BC-LEU-DEFG-W IN WHICH: X IS H, A PROTECTIVE GROUP OF THE N TERMINAL ATOM OF ACYL, AROMATIC URETHANE, ALIPHATIC URETHANE, ALKYL OR ARALKYL, OR A RESIDUE OF A NATURAL L-AMINO-ACID, THE FREE AMINO GROUP POSSIBLY PROTECTED BY A PROTECTIVE GROUP OF THE N-TERMINAL ATOM; A IS AN L-AMINO ACID RESIDUE OR A GLYCINE RESIDUE; B IS A NEUTRAL L-AMINO ACID RESIDUE; IT IS A NEUTRAL L-AMINO-ACID RESIDUE OR AN ACIDIC L-AMINO-ACID RESIDUE; D IS A L-AMINO-ACID RESIDUE WHICH CONTAINS IN THE SIDE CHAIN AN ALCOHOLIC HYDROXYL GROUP, THE LATEST BEING FREE OR PROTECTED BY A USUAL PROTECTION GROUP FOR THE HYDROXY FUNCTION, THIS PROTECTIVE GROUP BEING A TITYLE, TRUE, TRUE GROUP. BENZYL, 2,4-DICHLOROBENZYL, BENZYLOXYCARBONYL, 2-BROMOBENZYLOXYCARBONYL, T-BUTOXYCARBONYL OR LOWER ACYL; E IS A VALENCIA BOND OR A NEUTRAL L-AMINO-ACID RESIDUE; F IS A VALENCIA BOND OR L-AMINO-ACID RESIDUE; G IS A VALENCIA BOND OR A NEUTRAL L-AMINO-ACID RESIDUE; W IS OH, NH, OR, NHR, NR OR NH-NH-R; R IS AN ALKYL C-C GROUP SUBSTITUTED OR NON-SUBSTITUTED FOR A STRAIGHT CHAIN, A BRANCHED OR CYCLIC CHAIN (INCLUDING A MELTED OR PONTE RING), A PHENYL GROUP OR A C-C ARALKYL GROUP; R IS H, ONE OF THE BODIES SOMEWHAT REPRESENTED BY R, AN ALKYL CC ALIPHATIC GROUP WITH A STRAIGHT CHAIN, WITH A BRANCHED OR CYCLIC CHAIN (POSSIBLY SUBSTITUTED BY OH, NH OR A HALOGEN ATOM), AN ALKENYL CC GROUP, AN AROMATIC ACYL GROUP POSSIBLY SUBSTITUTES IN THE SAME MANNER, A GROUP OF THE ALIPHATIC CC URETHANE TYPE WITH A STRAIGHT CHAIN, A BRANCHED OR CYCLIC CHAIN, A GROUP OF THE AROMATIC URETHANE TYPE. THESE PEPTIDES CAN BE PREPARED BY CLASSIC SYNTHESIS IN SOLUTION OR BY SOLID PHASE SYNTHESIS ON POLYMERIC SUBSTRATES; THEIR PHARMACEUTICALLY ACCEPTABLE SALTS ARE FOR USE IN PHARMACEUTICAL COMPOSITIONS, IN PARTICULAR FOR THE RELEASE OF ACTH AND B-ENDORPHINE AND FOR THE INHIBITION OF THE RELEASE OF PROLACTIN. |
| priorityDate | 1982-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 319.