http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0709094-B1
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2ca2e4410855da087e11bf3eea8933fa |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-444 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-4439 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-439 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-4545 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-5377 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-55 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4439 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-444 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-439 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-55 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4545 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5377 |
filingDate | 1995-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2000-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ec86fba228b63a5c77094d4254e20171 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_284d0ee7ac4bab3c6ee4600ed98ad852 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c35fa40f365818e341676305f81c2822 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1f6149290dd43350e79c189d091a21c4 |
publicationDate | 2000-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | EP-0709094-B1 |
titleOfInvention | Tetrahydropyridine oxadiazole or thiadiazole compound for treating anxiety |
abstract | The present invention provides the use of a compound <CHEM> wherein Z1 is oxygen or sulphur; R is hydrogen, halogen, amino, -NHCO-R<2>, C3-7-cycloalkyl, C4-10-(cycloalkylalkyl), -Z<2>-C3-7-cycloalkyl optionally substituted with C1-6-alkyl, -Z<2>-C4-10-(cycloalkylalkyl), -Z<2>-C4-10-(cycloalkenylalkyl), -Z<2>-C4-10-(methylenecycloalkyl-alkyl), -NH-R2, -NR2R3, -NH-OR2, phenyl, phenoxy, benzoyl, benzyloxycarbonyl, tetrahydronaphtyl, indenyl, X, R<2>, -Z<2>R<2>, -SOR<2>, -SO2R<2>, -Z<2>-R<2>-Z<3>-R<3>, -Z<2>-R<2>-Z<3>-R<3>-Z<4>-R<4>, -Z<2>-R<2>CO-R<3>, -Z<2>-R<2>-CO2-R<3>, Z<2>-R<2>-O2C-R<3>, -Z<2>-R<2>-CONH-R<3>, -Z<2>-R<2>-NHCOR<3>, -Z<2>-R<2>-X, -Z<2>-R<2>-Z<3>-X, wherein Z<2>, Z<3>, and Z<4> independently are oxygen or sulphur, and R<2>, R<3> and R<4> independently are straight or branched C1-15-alkyl, straight or branched C2-15-alkenyl, straight or branched C2-15-alkynyl, each of which is optionally substituted with halogen(s), -OH, -CN, -CF3, -SH, -COOH, -NH-R<2>, -NR<2>R<3>, C1-6alkyl ester, one or two phenyl, phenoxy, benzoyl or benzyloxycarbonyl wherein each aromatic group is optionally substituted with one or two halogen, -CN, C1-4-alkyl or C1-4-alkoxy, and X is a 5 or 6 membered heterocyclic group containing one to four N, O or S atom(s) or a combination thereof, which heterocyclic group is optionally substituted at carbon or nitrogen atom(s) with straight or branched C1-6-alkyl, phenyl, benzyl or pyridine, or a carbon atom in the heterocyclic group together with an oxygen atom form a carbonyl group, or which heterocyclic group is optionally fused with a phenyl group; and R<5> and R<6> may be present at any position, including the point of attachment of the thiadiazole or oxadiazole ring, and independently are hydrogen, straight or branched C1-5-alkyl, straight or branched C2-5-alkenyl, straight or branched C2-5-alkynyl, straight or branched C1-10-alkoxy, straight or branched C1-5-alkyl substituted with -OH, -OH, halogen, -NH2 or carboxy; R<1> is hydrogen, straight or branched C1-5-alkyl, straight or branched C2-5-alkenyl or straight or branched C2-5-alkynyl; or a pharmaceutically acceptable salt or solvate thereof; for the manufacture of a medicament for the treatment of anxiety. |
priorityDate | 1994-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 900.