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filingDate 2000-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_18b48d6e55a965e2134fe1c9c3e790af
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f47aa5644e0bbef016ea62866a714e14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d94f4814ef02d5431a14c211071834e2
publicationDate 2003-02-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-0203839-A2
titleOfInvention 4-Phenyl-1-piperazinyl, piperidinyl and tetrahydropyridyl derivatives, pharmaceutical compositions containing them and their use
abstract The present invention relates to a novel group of halogen-substituted 4-phenyl-1-piperazinyl, piperidinyl, and tetrahydropyridyl derivatives having affinity for dopamine D4 receptors and D3 receptors. The compounds of the invention can be used to treat certain psychiatric and neurological disorders, including psychosis. In the compounds of the present invention, W is a carbon atom or a nitrogen atom or a methine group, and refers to a dotted line chemical bond from W when W is a carbon atom and does not represent a chemical bond when W is nitrogen or methine; R 1 and R 2 are independently hydrogen or halogen, with the proviso that at least one of R 1 and R 2 is halogen; R3 is hydrogen or halogen or alkyl, alkenyl, alkynyl, trifluoromethyl, alkoxy, aryloxy, aralkoxy, hydroxy, amino, alkylamino, dialkylamino, nitro or cyano; n is 2, 3, 4 or 5; X is oxygen or sulfur or carbonyl, thiocarbonyl, methylene, sulfinyl or sulfonyl; and Q is a group of formula (II) wherein Z is a 3- or 4-membered chain, wherein the chain members are selected from the group consisting of carbon, nitrogen, methine, methylene, carbonyl, and amine, with the proviso that only one of the chain moieties may be the nitrogen atom or imino group, and the Z chain may optionally contain one or two double bonds; R4, R5, R6, R7, R8 and R9 are independently hydrogen or halogen, or trifluoromethyl, nitro, cyano, alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylsulfonyl, hydroxy, hydroxyalkyl; , amino, alkylamino, dialkylamino, acyl, aminocarbonyl, alkylaminocarbonyl or dialkylaminocarbonyl; with the proviso that X is O or S when the Q group is attached via a nitrogen atom. The invention also encompasses pharmaceutical compositions containing the compounds. HE
priorityDate 1999-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457814461
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425386533
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10328
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID100861193
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID282365
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22029307
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2794881
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID141044595
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22029306
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID449204550
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421684627
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11952876
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394670
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID297
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22029333
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421687962
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11952837
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID402
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22029336
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419536132
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410893834
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421683324
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11952836
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22029335
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4829
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP51904
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421683321
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419533573
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP35395
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22029330
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ6UC74
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ28318
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421684625
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11952838
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421683329
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22029332
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID87111
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID452451264
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421613102
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22029331
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP48249
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13572639
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421613087
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9QZL1
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22029325

Total number of triples: 338.