Orally bioavailable potent soluble epoxide hydrolase inhibitors.
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Soluble epoxide hydrolase as a therapeutic target for cardiovascular diseasesDiscovery of inhibitors of soluble epoxide hydrolase: a target with multiple potential therapeutic indicationsThe molecular structure of epoxide hydrolase B from Mycobacterium tuberculosis and its complex with a urea-based inhibitorSynthesis and structure–activity relationship of piperidine-derived non-urea soluble epoxide hydrolase inhibitorsOptimized inhibitors of soluble epoxide hydrolase improve in vitro target residence time and in vivo efficacyCytochrome P450 epoxygenase pathway of polyunsaturated fatty acid metabolismMammalian soluble epoxide hydrolase is identical to liver hepoxilin hydrolaseSoluble epoxide hydrolase inhibitors and heart failureTargeting epoxides for organ damage in hypertensionSoluble epoxide hydrolase expression in a porcine model of arteriovenous graft stenosis and anti-inflammatory effects of a soluble epoxide hydrolase inhibitorSoluble epoxide hydrolase deficiency alters pancreatic islet size and improves glucose homeostasis in a model of insulin resistancePharmacokinetic optimization of four soluble epoxide hydrolase inhibitors for use in a murine model of inflammationInhibition of soluble epoxide hydrolase contributes to the anti-inflammatory effect of antimicrobial triclocarban in a murine modelInhibition of soluble epoxide hydrolase does not protect against endotoxin-mediated hepatic inflammationSoluble epoxide hydrolase inhibition modulates vascular remodelingInhibition of soluble epoxide hydrolase attenuates hepatic fibrosis and endoplasmic reticulum stress induced by carbon tetrachloride in micePeripheral FAAH and soluble epoxide hydrolase inhibitors are synergistically antinociceptiveInhibition of soluble epoxide hydrolase enhances the anti-inflammatory effects of aspirin and 5-lipoxygenase activation protein inhibitor in a murine modelPharmacokinetic screening of soluble epoxide hydrolase inhibitors in dogsBeneficial effects of soluble epoxide hydrolase inhibitors in myocardial infarction model: Insight gained using metabolomic approachesMultiphoton spectral analysis of benzo[a]pyrene uptake and metabolism in a rat liver cell lineVascular Endothelial Over-Expression of Human Soluble Epoxide Hydrolase (Tie2-sEH Tr) Attenuates Coronary Reactive Hyperemia in Mice: Role of Oxylipins and ω-HydroxylasesEDHF function in the ductus arteriosus: evidence against involvement of epoxyeicosatrienoic acids and 12S-hydroxyeicosatetraenoic acidSymmetric adamantyl-diureas as soluble epoxide hydrolase inhibitors.Inhibition of the soluble epoxide hydrolase promotes albuminuria in mice with progressive renal diseaseInhibition of soluble epoxide hydrolase by trans-4- [4-(3-adamantan-1-yl-ureido)-cyclohexyloxy]-benzoic acid is protective against ischemia-reperfusion injury.VN/14-1 induces ER stress and autophagy in HP-LTLC human breast cancer cells and has excellent oral pharmacokinetic profile in female Sprague Dawley ratsIncorporation of piperazino functionality into 1,3-disubstituted urea as the tertiary pharmacophore affording potent inhibitors of soluble epoxide hydrolase with improved pharmacokinetic properties.Hypoxia-induced pulmonary hypertension: comparison of soluble epoxide hydrolase deletion vs. inhibition.Inhibition of the soluble epoxide hydrolase attenuates monocrotaline-induced pulmonary hypertension in rats.Epoxyeicosatrienoic acid-dependent cerebral vasodilation evoked by metabotropic glutamate receptor activation in vivo.Soluble epoxide hydrolase inhibitor, t-TUCB, protects against myocardial ischaemic injury in rats.Soluble epoxide hydrolase inhibition is antinociceptive in a mouse model of diabetic neuropathy.Structure-activity relationships of substituted oxyoxalamides as inhibitors of the human soluble epoxide hydrolase.Screening a library of 1600 adamantyl ureas for anti-Mycobacterium tuberculosis activity in vitro and for better physical chemical properties for bioavailability.Metabolomics reveals increased isoleukotoxin diol (12,13-DHOME) in human plasma after acute Intralipid infusionThe lipophilic bullet hits the targets: medicinal chemistry of adamantane derivativesSynthesis and biological evaluation of sorafenib- and regorafenib-like sEH inhibitors.Identification of potent inhibitors of the chicken soluble epoxide hydrolase.Development of an online SPE-LC-MS-based assay using endogenous substrate for investigation of soluble epoxide hydrolase (sEH) inhibitors.
P2860
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P2860
Orally bioavailable potent soluble epoxide hydrolase inhibitors.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Orally bioavailable potent soluble epoxide hydrolase inhibitors.
@en
type
label
Orally bioavailable potent soluble epoxide hydrolase inhibitors.
@en
prefLabel
Orally bioavailable potent soluble epoxide hydrolase inhibitors.
@en
P2093
P2860
P356
P1476
Orally bioavailable potent soluble epoxide hydrolase inhibitors.
@en
P2093
Bruce D Hammock
Christophe Morisseau
Hsing-Ju Tsai
Jun-Yan Liu
Sung Hee Hwang
P2860
P304
P356
10.1021/JM070270T
P407
P577
2007-07-06T00:00:00Z