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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_2730eb4d055f672c506c6ca33137d3f9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_984aafeeac7dd9d640eaa3981e7bec48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6b6840df5b4ba406a4c95e808b8da04a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cd310cdbb0530a88e821212d18682b7e
publicationDate 2004-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SK-5212003-A3
titleOfInvention Metabotropic glutamate receptor antagonists
abstract The present invention concerns compounds of formula. In a preferable embodiment, X represents O; R<1> represents C1-6alkyl; cycloC3-12alkyl or (cycloC3-12alkyl)C1-6alkyl, wherein one or more hydrogen atoms in a C1-6alkyl-moiety or in a cycloC3-12alkyl-moiety optionally may be replaced by C1-6alkyloxy, aryl, halo or thienyl; R<2> represents hydrogen; halo; C1-6alkyl or amino; R<3> and R<4> each independently represent hydrogen or C1-6alkyl; or R<2> and R<3> may be taken together to form -R<2>-R<3>-, which represents a bivalent radical of formula -Z4-CH2-CH2-CH2- or -Z4-CH2-CH2- with Z4 being O or NR<11> wherein R<11> is C1-6alkyl; and wherein each bivalent radical is optionally substituted with C1-6alkyl; or R<3> and R<4> may be taken together to form a bivalent radical of formula -CH2-CH2-CH2-CH2- ; R<5> represents hydrogen; Y represents O; and aryl represents phenyl optionally substituted with halo. The invention also relates to the use of a compound according to the invention as a medicament and in the manufacture of a medicament for treating or preventing glutamate-induced diseases of the central nervous system, as well as formulations comprising such a compound and processes for preparing such a compound.
priorityDate 2000-10-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 418.