| Title : Synthesis and structure-activity relationship of piperidine-derived non-urea soluble epoxide hydrolase inhibitors - Pecic_2013_Bioorg.Med.Chem.Lett_23_417 |
| Author(s) : Pecic S , Pakhomova S , Newcomer ME , Morisseau C , Hammock BD , Zhu Z , Rinderspacher A , Deng SX |
| Ref : Bioorganic & Medicinal Chemistry Lett , 23 :417 , 2013 |
| Abstract : A series of potent amide non-urea inhibitors of soluble epoxide hydrolase (sEH) is disclosed. The inhibition of soluble epoxide hydrolase leads to elevated levels of epoxyeicosatrienoic acids (EETs), and thus inhibitors of sEH represent one of a novel approach to the development of vasodilatory and anti-inflammatory drugs. Structure-activities studies guided optimization of a lead compound, identified through high-throughput screening, gave rise to sub-nanomolar inhibitors of human sEH with stability in human liver microsomal assay suitable for preclinical development. |
| ESTHER : Pecic_2013_Bioorg.Med.Chem.Lett_23_417 |
| PubMedSearch : Pecic_2013_Bioorg.Med.Chem.Lett_23_417 |
| PubMedID: 23237835 |
| Gene_locus related to this paper: human-EPHX2 |
| Gene_locus related to this paper: human-EPHX2 |
Pecic S, Pakhomova S, Newcomer ME, Morisseau C, Hammock BD, Zhu Z, Rinderspacher A, Deng SX (2013)
Synthesis and structure-activity relationship of piperidine-derived non-urea soluble epoxide hydrolase inhibitors
Bioorganic & Medicinal Chemistry Lett
23 :417
Pecic S, Pakhomova S, Newcomer ME, Morisseau C, Hammock BD, Zhu Z, Rinderspacher A, Deng SX (2013)
Bioorganic & Medicinal Chemistry Lett
23 :417