http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101500986-A

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filingDate 2007-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9e7870de6fcd57e4bd6cab5ef59dfbae
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7923b0c4ac625f9b20c219d357a2a7fc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_671bd2b5899f3f81654a735b597a76ad
publicationDate 2009-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-101500986-A
titleOfInvention Di-aromatic substituted amides as inhibitors for GLYT1
abstract The present invention relates to compounds of the general Formula (I) wherein (A) is a 5 or 6-membered aromatic or heteroaromatic ring; R<1>is cycloalkyl or is aryl or heteroaryl, wherein at least one ring is aromatic in nature, unsubstituted or substituted by 1 to 3 substituents selected from the group consisting of halogen, lower alkyl, lower alkyl substituted by halogen, lower alkoxy, lower alkoxy substituted by halogen, -C(O) -lower alkyl, -S(O)2-lower alkyl, nitro or cyano; R<2> is hydrogen or lower alkyl; R<3> is hydrogen or lower alkyl; R<4> is halogen, lower alkyl, lower alkyl substituted by halogen, lower alkoxy, lower alkoxy substituted by halogen or nitro; R<5> is hydrogen, halogen, lower alkyl or lower alkyl substituted by halogen; X is a bond, -(CH2)m-, -CH2O- or -CH2NH-; The dotted line denotes a bond or not; n is 1 or 2; m is 1, 2 or 3; and pharmaceutically acceptable acid addition salts thereof and their use in the treatment of neurological and neuropsychiatric disorders.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103209964-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103288795-A
priorityDate 2006-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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