http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1687259-B1

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filingDate 2004-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5714b05db0b63c315cd4785793214698
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a615269361a8538a7b72dec8b5c16e03
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_683eddfb3e4874502ece9cb6e90eced4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_06bc1eff48b55e72cbf0611fe9db517e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_376b124b006b01c9e9beb15f08444323
publicationDate 2007-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1687259-B1
titleOfInvention Cyclopentyl derivates
abstract This invention is related to novel cyclopentyl derivatives of the following general formula (I) <CHEM> wherein X is methylene, oxygen, sulphur or a NR<7> group; R<1>   is a straight or branched C1-C8 alkyl or C3-C8 alkenylene or C3-C8 alkynylene chain, optionally substituted with CF3, phenyl, phenoxy or naphthyl, the aromatic rings optionally substituted by one or more C1-C4 alkyl, halogens, trifluoromethyl, hydroxy or C1-C4 alkoxy groups; R<2>, R<3>   are independently hydrogen, a C1-C3 alkyl chain,halogen, trifluoromethyl, hydroxy or C1-C4 alkoxy groups; R<4>, R<5>, R<6>, R<7>   are independently hydrogen or C1-C6 alkyl; and the pharmaceutically acceptable salts thereof that are active as sodium and/or calcium channel modulators and therefore useful in preventing, alleviating and curing a wide range of pathologies, including, but not limited to, neurological, psychiatric, cardiovascular, inflammatory, ophthalmic, urologic, metabolic and gastrointestinal diseases, where the above mechanisms have been described as playing a pathological role.
priorityDate 2003-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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