首页> 外国专利> Piperidinyl, indolyl, pirinidyl, morpholinyl and benzimidazolyl urea derivatives as inhibitors of soluble epoxide hydrolase for the treatment of hypertension, inflammations and other diseases

Piperidinyl, indolyl, pirinidyl, morpholinyl and benzimidazolyl urea derivatives as inhibitors of soluble epoxide hydrolase for the treatment of hypertension, inflammations and other diseases

机译:哌啶基,吲哚基,哌啶基,吗啉基和苯并咪唑基脲衍生物可作为可溶性环氧化物水解酶的抑制剂,用于治疗高血压,炎症和其他疾病

摘要

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.
机译:式(I)化合物;其中R是选自由C 1 -C 6烷基,芳基C 1 -C 6烷基,C 1 -C 7环烷基和杂环基组成的组的成员,Y选自由键,C(R),NR 3和O组成的组; Y选自由键,NR和O组成的组;每个R 1,R 2和R 3独立地选自H,烷基和COR; A是杂环基,任选地被1-2个R取代基取代; L选自由直接键,C 1 -C 6亚烷基,C 1杂亚烷基,C 1 -C 7亚环烷基,亚芳基,杂亚芳基,-CO-,-SO-和-Se-组成的组;要求保护的R选自H,C 1 -C 6烷基,C 1 -C 6烯基,C 1 -C 6炔基,C 1-杂烷基,芳基C 1 -C 6烷基,C 1,环烷基和杂环基。这些化合物是可溶性环氧化物水解酶(sEH)的抑制剂,可用于治疗高血压,炎症,成人呼吸窘迫综合征;糖尿病并发症;晚期肾脏疾病;雷诺综合症和关节炎。

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