Structure-based optimization of arylamides as inhibitors of soluble epoxide hydrolase
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Discovery of inhibitors of soluble epoxide hydrolase: a target with multiple potential therapeutic indicationsImpact of soluble epoxide hydrolase and epoxyeicosanoids on human healthDiscovery of MK-8718, an HIV Protease Inhibitor Containing a Novel Morpholine Aspartate Binding GroupInhibition of soluble epoxide hydrolase by fulvestrant and sulfoxidesFragment Screening of Soluble Epoxide Hydrolase for Lead Generation-Structure-Based Hit Evaluation and Chemistry Exploration18F-FNDP for PET Imaging of Soluble Epoxide Hydrolase (sEH)Incorporation of piperazino functionality into 1,3-disubstituted urea as the tertiary pharmacophore affording potent inhibitors of soluble epoxide hydrolase with improved pharmacokinetic properties.Structure-activity relationships of substituted oxyoxalamides as inhibitors of the human soluble epoxide hydrolase.The role of epoxide hydrolases in health and disease.Single-residue posttranslational modification sites at the N-terminus, C-terminus or in-between: To be or not to be exposed for enzyme accessFörster resonance energy transfer competitive displacement assay for human soluble epoxide hydrolase.Investigating Structural Requirements for the Antiproliferative Activity of Biphenyl Nicotinamides.Investigation of the binding mode of 1, 3, 4-oxadiazole derivatives as amide-based inhibitors for soluble epoxide hydrolase (sEH) by molecular docking and MM-GBSA.Microsomal cytochrome P450 as a target for drug discovery and repurposing.1-Aryl-3-(1-acylpiperidin-4-yl)urea inhibitors of human and murine soluble epoxide hydrolase: structure-activity relationships, pharmacokinetics, and reduction of inflammatory pain.Discovery of the first dual inhibitor of the 5-lipoxygenase-activating protein and soluble epoxide hydrolase using pharmacophore-based virtual screeningMolecular Imaging of Hydrolytic Enzymes Using PET and SPECT.1-(1-acetyl-piperidin-4-yl)-3-adamantan-1-yl-urea (AR9281) as a potent, selective, and orally available soluble epoxide hydrolase inhibitor with efficacy in rodent models of hypertension and dysglycemiaA systematic analysis of atomic protein-ligand interactions in the PDB.Novel piperidine-derived amide sEH inhibitors as mediators of lipid metabolism with improved stability.Metabolism-guided drug designIn Vitro and In Silico Insights into sEH Inhibitors with Amide-Scaffold from the Leaves of Capsicum chinense Jacq
P2860
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P2860
Structure-based optimization of arylamides as inhibitors of soluble epoxide hydrolase
description
2009 nî lūn-bûn
@nan
2009 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Structure-based optimization of arylamides as inhibitors of soluble epoxide hydrolase
@ast
Structure-based optimization of arylamides as inhibitors of soluble epoxide hydrolase
@en
Structure-based optimization of arylamides as inhibitors of soluble epoxide hydrolase
@nl
type
label
Structure-based optimization of arylamides as inhibitors of soluble epoxide hydrolase
@ast
Structure-based optimization of arylamides as inhibitors of soluble epoxide hydrolase
@en
Structure-based optimization of arylamides as inhibitors of soluble epoxide hydrolase
@nl
prefLabel
Structure-based optimization of arylamides as inhibitors of soluble epoxide hydrolase
@ast
Structure-based optimization of arylamides as inhibitors of soluble epoxide hydrolase
@en
Structure-based optimization of arylamides as inhibitors of soluble epoxide hydrolase
@nl
P2093
P356
P1476
Structure-based optimization of arylamides as inhibitors of soluble epoxide hydrolase
@en
P2093
Alison Kukulka
Anne B Eldrup
Chuk C Man
David Joseph
Fariba Soleymanzadeh
Ingo Muegge
Keith McKellop
Neil A Farrow
Steven J Taylor
Stéphane De Lombaert
P304
P356
10.1021/JM9005302
P407
P577
2009-10-08T00:00:00Z