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Volumn 48, Issue 4-5, 2013, Pages 619-627

Substituted phenyl groups improve the pharmacokinetic profile and anti-inflammatory effect of urea-based soluble epoxide hydrolase inhibitors in murine models

Author keywords

Anti inflammation; Bioavailability; Eicosanoids; Metabolic profiling; Pharmacokinetics

Indexed keywords

1 (1 ACETYLPIPERIDIN 4 YL) 3 ADAMANTANYLUREA; 1 (1 METHANESULFONYLPIPERIDIN 4YL) 3 (4 TRIFLUOROMETHOXYPHENYL)UREA; 1 (4 TRIFLUOROMETHOXYPHENYL) 3 (1 CYCLOPROPANECARBOXYLPIPERIDIN 4 YL)UREA; 1 (4 TRIFLUOROMETHOXYPHENYL) 3 [(1YL UREIDO)CYCLOHEXYLOXY]BENZOIC ACID; 1 CHLOROPHENYL 3 (1 PROPIONYLPIPERIDIN 4 YL)UREA; 1 TRIFLUOROMETHOXYPHENYL 3 (1 PROPIONYLPIPERIDIN 4 YL)UREA; 4 [4 [3 (1 ADAMANTYL)UREIDO]CYCLOHEXYLOXY]BENZOIC ACID; ANTIINFLAMMATORY AGENT; EPOXIDE; GAMMA INTERFERON; HYDROLASE INHIBITOR; INTERLEUKIN 6; LIPOPOLYSACCHARIDE; MONOCYTE CHEMOTACTIC PROTEIN 1; OXYLIPIN; TUMOR NECROSIS FACTOR ALPHA; UNCLASSIFIED DRUG;

EID: 84873462464     PISSN: 09280987     EISSN: 18790720     Source Type: Journal    
DOI: 10.1016/j.ejps.2012.12.013     Document Type: Article
Times cited : (64)

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