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filingDate 1996-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b33adf279dcf0ef6849d3717b1c9513
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9cf65da26404caedcb7e190baac1bbfb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_123b8ffcaf5460cda2002f105db51a95
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_123e73e40f33cd0f4b9dbb3faea3fa9d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5ea65773b0cbcd5b07839bf1fdc21b8f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fcb9fa3693b0b369da99f23c84383617
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_87e0384ab9d6f439d7ca52dbbaecbfa6
publicationDate 2004-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-223601-B1
titleOfInvention 5-HT receptor antagonist indole derivatives
abstract The compounds of the present invention and their pharmaceutically acceptable salts of formula (I) are P1 and P2 phenyl or heterocyclic; A bond is an optionally substituted chain or A is optionally substituted phenyl or heterocyclic; R1 and R2 are hydrogen, optionally alkyl, alkenyl, alkynyl, alkylthio, cyano, nitro, halogen, trifluoromethyl, pentafluoroethyl, NR12R13, CONR12R13, NR12COR13, S (O) pNR12R13, formyl, trifluoromethoxy, trifluoromethylthio, COR14, CH2R14, CH2OR14, CO2R14 or OR14, wherein p1 or 2, R12, R13 and R14 are hydrogen, alkyl, optionally substituted aryl; or aryl (C 1 -C 6) alkyl; n and m are 0, 1 or 2; R3 is hydrogen or alkyl; R4 is a group of formula (i), X and Y are nitrogen, or one is nitrogen and the other is CR5 or one is CR5 and the other is carbon or CR5; R5, R6, R7 and R8 are hydrogen; substituted alkyl, alkenyl, cycloalkyl, cycloalkylalkoxy, alkynyl, cycloalkoxy, cycloalkylalkyl, alkylthio, cycloalkylthio, cycloalkylalkylthio, alkoxy, hydroxy; , halogen, nitro, trifluoromethoxy, trifluoromethylthio, trifluoromethylsulfonyl, fluorosulfonyl, formyl, alkanoyl, cyano, phenyl or thienyl, NR12R13, CONR12R13 or CO2R14, R12, R13 and R14 are as defined for R1; or R6 and R7 are part of an optionally substituted ring group; and R9 and R10 are hydrogen or alkyl. The present invention encompasses processes for the preparation of the compounds, pharmaceutical compositions containing the compounds, and the use of the compounds and pharmaceutical compositions for the treatment of central nervous system disorders such as anxietas. ŕ
priorityDate 1995-02-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 517.