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filingDate 2001-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d78e03cc1e994a21bd7dace1921ad8ff
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_571a56049700f9445fe2bc753adf02d4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0924238925f2d489ab6de51c25dbd740
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_01d467c8ab43b6003a42cf8de7b47771
publicationDate 2002-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2415673-A1
titleOfInvention Tetrazole derivatives
abstract The present invention is concerned with 2H-tetrazole-5-yl-amide derivatives of general formula (I) wherein R1 signifies hydrogen, lower alkyl, -(CH2)n-CF3, - (CH2)n-CHF2, -(CH2)n-CN, -(CH2)n-cycloalkyl, -(CH2)n-O-lower alkyl, -(CH2)n- O- cycloalkyl or -(CH2)n-C(O)O-lower alkyl; R2 signifies hydrogen, lower alkyl, lower alkoxy, halogen, -C(O)-lower alkyl, -C(O)OH, -C(O)O-lower alkyl, -NR3R 4 or -C(O)-NR3R4 and wherein R3 and R4 may be independently from each other hydrogen or lower alkyl; X signifies -O-, -S-, -CH2, -OCH2- or two hydrogen atoms not forming a bridge; and n signifies 0, 1, 2, 3 or 4; as well as with their pharmaceutically acceptable salts. It has been found that the compound s of general formula (I) are group 1 metabotropic glutamate receptor agonists (mGluR) and are therefore useful in the treatment of corresponding CNS- disorders.
priorityDate 2000-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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