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filingDate 2000-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2004-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4adcd31e3b2ff98f8bcc39b8eb11755a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0924238925f2d489ab6de51c25dbd740
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8f6977df5a366198752fcb938255a3f3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d1b625e5fb6dbd07db96e144cad27535
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_950de802da23d33641f68d1e4492a703
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2e6de93399b16fca8512d7b71b40edec
publicationDate 2004-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2209728-T3
titleOfInvention TETRAHYDRO-BENZO (D) AZEPINAS AND ITS USE AS ANTAGONISTS OF METABOTROPIC GLUTAMATE RECEPTORS.
abstract Compounds of the ** formula ** wherein R1 means hydrogen, C1-7 alkyl, oxygen, halogen, or -OR, -O (C3-C6) cycloalkyl, -O (CHR) n- (C3-C6) cycloalkyl, -O (CHR) nCN, -O (CHR) nCF3, -O (CHR) - (CHR) nNR2, -O (CHR) (CHR) nOR, -O (CHR) n-C2-7 alkenyl, -OCF3, -OCF2-R, -OCF2-C2-7 alkenyl, -OCHRF, -OCHF-C2-7 alkenyl, -OCF2CRF2, -OCF2Br, -O (CHR) nCF2Br, -O (CHR) n-phenyl, where the group Phenyl may optionally be substituted independently of one another by one to three C1-7 alkyl, C1-7 alkoxy, halogen, nitro or cyano groups, as well as their pharmaceutically acceptable salts in their racemic and optically active form.
priorityDate 1999-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 724.