http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2007207053-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/A61K31-437
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-28
filingDate 2007-01-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5d765946d0f18275765aa09d565a13c4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd53ce2c4146d033830f604a531158d1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6d361c8cd448909c6953bdb08cd51e78
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e9a7fd2923c9bdbac3f262bd97957c0e
publicationDate 2012-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2007207053-B2
titleOfInvention Aryl-isoxazol-4-yl-imidazo[1,2-a]pyridine useful for the treatment of Alzheimer's disease via GABA receptors
abstract The present invention is concerned with aryl-isoxazol-4-yl-imidazo[1,2-a]pyridine derivatives of formula (I): wherein R is hydrogen, halogen, hydroxy, lower alkyl, benzyloxy or -O-(CH)-(CO)-5 or 6 membered heteroaryl optionally substituted by aryl or by lower alkyl; R is hydrogen, halogen, lower alkyl, lower alkynyl, amino, -NHC(O)-R or -(CO)-R; R is hydrogen, halogen, cyano, lower alkyl, lower alkynyl, amino, -NHC(O)-R, -(CO)-R, -5 or 6-membered heterocycloalkyl in 1-position, optionally substituted 10 by =O or is a -5 or 6-membered heteroaryl in 1-position; R is hydrogen or -5 or 6-membered heteroaryl; R is lower alkyl or cycloalkyl; R is lower alkoxy or NR'R'', wherein R' and R'' are each independently hydrogen, lower alkyl optionally substituted by hydroxy, lower alkynyl, -(CH)-cycloalkyl, 15 -(CH)-5 or 6-membered heterocycloalkyl or -(CH)-5 or 6-membered heteroaryl; n is 0 to 3; as well as 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 2006-01-17-04:00^^<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/compound/CID24739145
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410517824
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19509
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3373
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID737487
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID86613561
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69072661
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID453308408
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416168351
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID61055
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID338536
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24738991
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID168937
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3438

Total number of triples: 311.