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filingDate 2001-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2010-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b21500fa13f2bbde97732750f4f59c8b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_47606d15bd40781659ae8a2527bd1c1b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3ef212d5a40a03f55ff57d192ff37755
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f45ef57bc10945f4825a1af9eea7ce9
publicationDate 2010-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2398765-C1
titleOfInvention Azacyclic compounds to be used in treating serotonin-mediated diseases
abstract FIELD: medicine, pharmaceutics. n SUBSTANCE: invention refers to new compounds of formula (I) , where Z means where R means hydrogen, C 4 -C 6 cycloalkyl group attached either through one of ring carbon atoms, or through a lower alkylene group attached to the ring, or a linearly chained or branched lower alkyl group or a lower hydroxyalkyl group, or a lower aminoalkyl group, or a phenyl(lower alkyl) group optionally substituted with 1-2 substitutes chosen from lower alkyl, lower alkoxy, halogen and hydroxy, or heteroaryl(lower alkyl)group where heteroaryl is chosen from the group consisting from thienyl, substituted with lower alkyl group, imidazolyl, and thiazolyl substituted with the lower alkyl group; n means 0 or 1; or Z means a group where R means the lower alkyl group; X 1 means methylene or NH group; and X 2 means methylene; or X 1 means methylene and X 2 means methylene or a bond; or X 1 means methylene, and X 2 means O, S or a bond; Y 1 means methylene, and Y 2 means methylene, vinylene, ethylene, or a bond; Ar 1 means unsubstituted or substituted phenyl; Ar 2 means unsubstituted or substituted phenyl, unsubstituted or substituted thienyl, unsubstituted or substituted furyl, unsubstituted or substituted pyridyl; and when Ar 1 and Ar 2 are substituted, each Ar 1 and Ar 2 are independently substituted with one or more substituted chosen from lower alkyl, lower alkoxy, hydroxy, lower hydroxyalkyl, halogen, di- and trihaloalkyl, di- and trihaloalkoxy, mono- and dialkylamino, alkilthio, alkyl ester and nitro; provided that Ar 1 and Ar 2 do not simultaneously mean unsubstituted phenyl; W means oxygen or sulphur; or to their pharmaceutically acceptable salts; provided those specified in cl. 1 of the patent claim. Besides the invention concerns the compounds chosen from the group, to compounds of formula (I), to pharmaceutical compositions, to a method of inhibition of monoamine receptor activity, to a method of inhibition of monoamine receptor activation, to a method of treating a diseased state associated with serotonin receptor, to a method of treating schizophrenia, to a method of treating migraine, and also to a method of treating psychosis. n EFFECT: preparation of the new biologically active compounds capable to inhibit monoamine receptor activity. n 65 cl, 140 ex, 5 tbl
priorityDate 2000-03-06-04:00^^<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: 753.