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filingDate 2005-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a8878c3e3af8836d44722e0ef5400809
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publicationDate 2007-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-PI0507746-A
titleOfInvention compound or a salt, prodrug or solvate thereof, pharmaceutical composition, method of treating glk-mediated diseases, and process for the preparation of a compound
abstract COMPOUND OR A SALT, PRODUCT OR SOLVATE OF THE SAME, PHARMACEUTICAL COMPOSITION, METHOD OF TREATING GLK-MEDIATED DISEASES, AND PROCESS FOR PREPARING A COMPOUND wherein R¬ 1¬ is methoxymethyl; R¬ 2¬ is selected from -C (O) NR¬ 4¬R¬ 5¬, -SOÐR¬ 4¬R¬ 5¬, -S (O) <sym> R¬ 4¬ and HET-2; HET-1 is an optionally substituted 5 or 6 membered C-linked heteroaryl ring; HET-2 is an optionally substituted 4-, 5- or 6-membered C- or N-linked heterocyclyl ring; R¬ 3¬ is selected from halo, fluoromethyl, difluoromethyl, trifluoromethyl, methyl, methoxy and cyano; R¬4¬ is selected, for example, from hydrogen, optionally substituted (1-4C) alkyl and HET-2; R¬5¬ is hydrogen or (1-4C) alkyl or R¬4¬ and R¬5¬ together with the nitrogen atom to which they are attached may form a heterocyclyl ring system as defined by HET-3; HET-3 is, for example, an optionally substituted 4-, 5- or 6-membered saturated or partially unsaturated heterocyclyl ring; p is (regardless of each occurrence) 0, 1 or 2; m is 0 or 1; n is 0, 1 or 2; provided that when m is 0, then n will be 1 or 2 or a salt, prodrug or solvate thereof, are described. Their use as GLK activators, pharmaceutical compositions containing them and processes for their preparation are also described.
priorityDate 2004-02-18-04:00^^<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: 41.