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filingDate 2002-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2005-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0924238925f2d489ab6de51c25dbd740
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f51205ece3ac1cdc92d1c512faa6d3f4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_950de802da23d33641f68d1e4492a703
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_037e59f9554c70ff97c56559eee6d3ba
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_571a56049700f9445fe2bc753adf02d4
publicationDate 2005-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2235044-T3
titleOfInvention DERIVATIVES OF DIHIDRO-BENZO (B) (1,4) -DIAZEPIN-2-ONA AS ANTAGONISTS I OF MGLUR2.
abstract Compounds of the general formula ** (Formula) ** wherein R 1 is cyano, C 1-7 fluor-alkyl, C 1-7 alkoxy, C 1-7 fluor-alkoxy or is pyrrol-1-yl, which is unsubstituted or substituted with one to three substituents selected from the group consisting of fluorine, chlorine, cyano, phenyl optionally substituted with halogen, - (CH2) 1-4-hydroxyl, fluor-C1-7 alkyl, C1, 7 alkyl, - (CH2) n- C1-7 alkoxy, - (CH2) nC (O) OR¿, - (CH2) 1-4-NR¿R¿, hydroxy-C1-7 alkoxy, and - (CH2) n-CONR¿R¿; is hydrogen, if R1 is optionally substituted pyrrol-1-yl, as defined above, or is halogen, hydroxyl, C1-7 alkyl, fluorine C1-7 alkyl, C1-7 alkoxy, hydroxymethyl, hydroxyethoxy, C1 alkoxy , 7- (ethoxy) n (n = 1 to 4), C1-7 alkoxymethyl, cyanomethoxy, morpholin-4-yl, thiomorpholin-4-yl, 1-oxothiomorpholin-4-yl, 1, 1-dioxothiomorpholin-4- ilo, 4-oxo-piperidin-1-yl, 4-alkoxy-piperidin-1-yl, 4-hydroxy-piperidin-1-yl, 4-hydroxyethoxy-piperidin-1-yl, 4-C1-alkyl, 7-piperazin -1-yl.
priorityDate 2001-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422383518
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID790333
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419489467
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID153776172
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424736607
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419849152
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413371329
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22224947
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422383519
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22317495
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9867404
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18548787
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9845
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID153776174
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419849156
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18548754
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID159447829
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425998304
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID153776175
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419849157
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18548755
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416014459
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID153776176
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419849158
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18548756
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392451
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18548757
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11816148
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419514433
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411836485
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22224638
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454591293
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424365406
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424346202

Total number of triples: 638.