21 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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1,3-Disubstituted and 1,3,3-trisubstituted adamantyl-ureas with isoxazole as soluble epoxide hydrolase inhibitors.
University of California Davis
Optimized inhibitors of soluble epoxide hydrolase improve in vitro target residence time and in vivo efficacy.
University of California Davis
Synthesis and Evaluation of Quinazolines as Inhibitors of the Bacterial Cell Division Protein FtsZ.
University of California Davis
Orally bioavailable potent soluble epoxide hydrolase inhibitors.
University of California Davis
Novel flavonoids with antiproliferative activities against breast cancer cells.
University of California Davis
Selectively targeting T- and B-cell lymphomas: a benzothiazole antagonist of alpha4beta1 integrin.
University of California Davis
Design, synthesis, and biological activity of 1,3-disubstituted ureas as potent inhibitors of the soluble epoxide hydrolase of increased water solubility.
University of California Davis
Development of potent inhibitors of the human microsomal epoxide hydrolase.
University of California Davis
Bioisosteric substitution of adamantane with bicyclic lipophilic groups improves water solubility of human soluble epoxide hydrolase inhibitors.
University of California Davis
Imidazolidine-2,4,5- and pirimidine-2,4,6-triones - New primary pharmacophore for soluble epoxide hydrolase inhibitors with enhanced water solubility.
University of California Davis
Click-based synthesis of triazolobithiazole ΔF508-CFTR correctors for cystic fibrosis.
University of California Davis
Structure-activity relationships of cyanoquinolines with corrector-potentiator activity in ΔF508 cystic fibrosis transmembrane conductance regulator protein.
University of California Davis
Fluorinated ΔF508-CFTR correctors and potentiators for PET imaging.
University of California Davis
Pyrazolylthiazole as DeltaF508-cystic fibrosis transmembrane conductance regulator correctors with improved hydrophilicity compared to bithiazoles.
University of California Davis
Identification and optimization of soluble epoxide hydrolase inhibitors with dual potency towards fatty acid amide hydrolase.
University of California Davis
Adamantyl thioureas as soluble epoxide hydrolase inhibitors.
University of California Davis
Orally Available Soluble Epoxide Hydrolase/Phosphodiesterase 4 Dual Inhibitor Treats Inflammatory Pain.
University of California Davis
