http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2601951-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_27a71ddaaa2f5a8c228fc6cb3f3b3098 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-06 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-415 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-06 |
| filingDate | 1987-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a81a3f528f05f7e81f18bbd04e3156e8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_095ca94623df321d95577e61eabe5425 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1931093a8c6cc1351f2f567e086d6f6e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8a1a739cab96da23ffbdde1932dbe63d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b4d467b93b7133bf27b44df47fc3f610 |
| publicationDate | 1988-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | FR-2601951-A1 |
| titleOfInvention | NOVEL TETRAHYDROCARBAZOLONES, PHARMACEUTICAL COMPOSITION CONTAINING SAME AND PROCESS FOR PREPARING THE SAME |
| abstract | THE PRESENT INVENTION CONCERNS TETRAHYDROCARBAZOLONES OF FORMULA I: (CF DRAWING IN BOPI) R REPRESENTS H OR A GROUP OF CAC ALCOHOL, CAC CYCLOALCOYL, CA CYCLOALCOYL C-ALCOYL EN CYNAC, ALCENYL, PHYLEN CAC, CAC ALCENYL -ALCOYL EN CAC, -COR, -COR, -CONRR OR -SOR (OR R AND R, WHICH MAY BE THE SAME OR DIFFERENT, EACH REPRESENTS A HYDROGEN ATOM, A CAC ALCOHOL GROUP OR A CAC CYCLOALCOYL OR A PHENYL GROUP OR PHENYL-ALCOYL IN CAC IN WHICH THE PHENYL GROUP IS POSSIBLE SUBSTITUTED BY ONE OR MORE GROUPS OF CAC ALCOHYL, CAC ALCOXY OR HYDROXY OR HALOGEN ATOMS, WITH THIS PRECISION THAT R DOES NOT REPRESENT A REPRESENT OF HORSYD ATOMES A -COR OR -SOR GROUP); ONE OF THE GROUPS REPRESENTED BY R, R AND R IS H OR A GROUP ALCOYL IN C A C, CYCLOALCOYL IN C A C, ALCENYL IN C A C OR PHENYL-ALCOYL IN C A C AND EACH OF THE TWO OTHER GROUPS REPRESENTS INDEPENDENTLY A C A C HYDROALCOYL; R REPRESENTS A C A C ALCOHYL, AND THEIR PHYSIOLOGICALLY ACCEPTABLE SALTS AND SOLVATION PRODUCTS. THE COMPOUNDS ARE POWERFUL AND SELECTIVE ANTAGONISTS OF THE EFFECT OF 5-HT IN 5-HT RECEPTORS AND ARE USEFUL, FOR EXAMPLE, IN THE TREATMENT OF PSYCHOTROPIC DISEASES, ANXIETY, AND NAUSEA AND VOMITING . THE PRESENT INVENTION ALSO CONCERNS A PHARMACEUTICAL COMPOSITION CONTAINING THEM AND A PROCESS FOR THEIR PREPARATION. |
| priorityDate | 1986-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 74.