http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2006331437-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-28
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-42
filingDate 2006-12-14^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-07-05^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e9a7fd2923c9bdbac3f262bd97957c0e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6d361c8cd448909c6953bdb08cd51e78
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd53ce2c4146d033830f604a531158d1
publicationDate 2012-07-05^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2006331437-B2
titleOfInvention Aryl-Isoxazol-4-yl-Imidazole derivatives
abstract The present invention is concerned with aryl-isoxazol-4-yl-imidazole derivatives of formula (I), wherein R to R are each independently hydrogen or halogen; R is hydrogen, lower alkyl, cycloalkyl, -(CH)-O-lower alkyl or lower alkyl substituted by hydroxy; R is -(CH)-aryl or -(CH)-heteroaryl which are optionally substituted by one or more substituents selected from the group consisting of halogen, cyano, nitro, lower alkyl, lower alkoxy, lower alkylsulfanyl, lower alkyl substituted by halogen, -C(O)-lower alkyl, -C(O)-O-lower alkyl, -NH-C(O)-O-lower alkyl or -C(O)-NH-R', wherein R' is lower alkynyl or lower alkyl substituted by halogen, or is -(CH)-cycloalkyl, -(CH)-heterocyclyl, -(CH)-heteroaryl or -(CH)-aryl, optionally substituted by halogen; R is hydrogen, -C(O)H, -(CH)-O-lower alkyl, -C(O)O-lower alkyl, lower alkyl substituted by hydroxy or halogen, or is cycloalkyl, aryl, or is -(CH)-O-CH-aryl, optionally substituted by halogen or lower alkyl, or is -(CH)-O-CH-heteroaryl, optionally substituted by halogen, lower alkyl or lower alkyl substituted by halogen, or is -(CH)-NH-(CH)-heterocyclyl; n is 0, 1, 2 or 3 m is 0 or 1; o is 1, 2 or 3; as well as with pharmaceutically acceptable acid addition salts thereof. It has been found that this class of compounds show high affinity and selectivity for GABA A α5 receptor binding sites and might be useful as cognitive enhancer or for the treatment of cognitive disorders like Alzheimer's disease.
priorityDate 2005-12-27^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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