PMID

Data

Article Title

Organization

Two Potent OXE-R Antagonists: Assignment of Stereochemistry.

Florida Institute of Technology

Base-dependent formation of cis and trans olefins and their application in the synthesis of 5-oxo-ETE receptor antagonists.

Florida Institute of Technology

Inhibition of 5-oxo-6,8,11,14-eicosatetraenoic acid-induced activation of neutrophils and eosinophils by novel indole OXE receptor antagonists.

Mcgill University

5-Oxo-ETE receptor antagonists.

Florida Institute of Technology

C20-trifluoro-5-oxo-ETE: a metabolically stable 5-oxo-ETE derivative.

Florida Institute of Technology

5-oxo-15-HETE: total synthesis and bioactivity.

Florida Institute of Technology

Novel Highly Potent and Metabolically Resistant Oxoeicosanoid (OXE) Receptor Antagonists That Block the Actions of the Granulocyte Chemoattractant 5-Oxo-6,8,11,14-Eicosatetraenoic Acid (5-oxo-ETE).

Florida Institute of Technology

Synthesis, molecular modelling studies and biological evaluation of new oxoeicosanoid receptor 1 agonists.

Hospital Del Mar Medical Research Institute (Imim)

Structure-activity relationship study ofβ-oxidation resistant indole-based 5-oxo-6,8,11,14-eicosatetraenoic acid (5-oxo-ETE) receptor antagonists.

Florida Institute of Technology

Identification of a novel human eicosanoid receptor coupled to G(i/o).

Tanabe Seiyaku