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filingDate 2007-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_62b22ea5d7765b4c3bc6a497200bb37a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3f230f5b6adb34634c10709d7d7fba8c
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publicationDate 2012-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2007225170-B2
titleOfInvention Piperidinyl, indolyl, pirinidyl, morpholinyl and benzimidazolyl urea derivatives as inhibitors of soluble epoxide hydrolase for the treatment of hypertension, inflammations and other diseases
abstract Compounds of the formula (I); wherein R is a member selected from the group consisting of C-Calkyl, arylC-Calkyl, C-Ccycloalkyl and heterocyclyl, Y is selected from the group consisting of a bond, C(R), NR and O; Y is selected from the group consisting of a bond, NR and O; each R, R and R is independently selected from the group consisting of H, alkyl and COR; A is heterocyclyl, optionally substituted with from 1 to 2 R substituents; L is selected from the group consisting of a direct bond, C-Calkylene, CCheteroalkylene, C-Ccycloalkylene, arylene, heteroarylene, -CO-, -SO- and -Se-; R is selected from the group consisting of H, CCalkyl, C-Calkenyl, C-Calkynyl, C,-Cheteroalkyl, arylC-Calkyl, CC,cycloalkyl and heterocyclyl, are claimed. The compounds are inhibitors of the soluble epoxide hydrolase (sEH) and useful for the treatment of hypertension, inflammation, adult respiratory distress syndrome; diabetic complications; end stage renal disease; Raynaud syndrome and arthritis.
priorityDate 2006-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 561.