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filingDate 2007-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2d000e3f29e7ef872de709c3fcd85e1d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9173a65704e2ba683ce35ba176ecd1b4
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publicationDate 2011-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2437872-C2
titleOfInvention Substituted phenyl methanone derivatives
abstract FIELD: chemistry. ^ SUBSTANCE: invention relates to novel phenyl methanone derivatives of the formula I: where R1 denote -OR1, heterocycle such as morpholinyl, pyrrolidinyl, tetrahydropyranyl, phenyl, heteoaryl such as pyrazolyl, which are not substituted or substituted with C1-6alkyl, halogen; R1 denote C1-6alkyl, C1-6alkyl substituted with halogen, or denotes a -(CH2)0-saturated C3-6cycloalkyl; R2 denotes -S(O)2-C1-6alkyl, -S(O)2NH-C1-6alkyl, NO2 or CN; R3 denotes pyridinyl, substituted with C1-6alkyl, substituted with halogen, or phenyl which is not substituted or substituted with one to three substitutes selected from a group consisting of C1-6alkyl, C1-6alkoxy, CN, NO2, halogen, C1-6alkyl, substituted with halogen, C1-6alkoxy, substituted with halogen, phenyl, sulphonamide; X denotes -CH2-, -NH-, -CH2O- or -OCH2-; n denotes 1, 2; m denotes 1, 2; o denotes 1 or 1; and pharmaceutically acceptable acid addition salt thereof. ^ EFFECT: compounds have glycine reuptake inhibition which enables their use to prepare a pharmaceutical composition. ^ 9 cl, 2 tbl, 40 ex
priorityDate 2006-06-22-04:00^^<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/compound/CID59030462

Total number of triples: 298.