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filingDate 2001-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dbe4be4ececda72c944054da8cc76adc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6b6840df5b4ba406a4c95e808b8da04a
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2730eb4d055f672c506c6ca33137d3f9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_984aafeeac7dd9d640eaa3981e7bec48
publicationDate 2006-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EA-007464-B1
titleOfInvention ANTAGONISTS OF METABOTROPIC GLUTAMAT RECEPTORS
abstract The present invention relates to compounds of the formula (I-A) and (I-B). In a preferred embodiment, X is O; R 1 is C 1-6 alkyl; cycloSalkyl or (cycloSalkyl) C1-6alkyl, wherein one or more hydrogen atoms in the C1-6alkyl or cycloalkylalkyl moieties may optionally be substituted by C1-6alkyloxy, aryl, halogen or thienyl; Is hydrogen; halogen; C1-6alkyl or amino; R and R are independently hydrogen or C1-6alkyl; either R and R, taken together, can form a —RR— group, which is a divalent radical of the formula —Z — CH — CH — CH— or —Z — CH — CH—, where Z is O or NR, where R is C 1-6 alkyl, each divalent the radical is optionally substituted with C1-6alkyl; or R and R, taken together, can form a divalent radical of the formula —CH — CH — CH — CH — CH—; Is hydrogen; Y represents O; and aryl is phenyl optionally substituted with halogen. The present invention also relates to the use of a compound of this invention as a medicament and to the manufacture of a medicament for the treatment or prophylaxis of glutamate-induced diseases of the central nervous system, as well as to pharmaceutical preparations containing such a compound, and to methods for producing such a compound.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2720205-C2
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priorityDate 2000-10-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 393.