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Targeting the OXE receptor with a selective antagonist inhibits allergen‐induced pulmonary inflammation in non‐human primates

British journal of pharmacology, 2022-01, Vol.179 (2), p.322-336

2022

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The eosinophil chemoattractant 5-oxo-ETE and the OXE receptor

Progress in lipid research, 2013-10, Vol.52 (4), p.651-665

2013

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Targeting the OXE receptor as a potential novel therapy for asthma

Biochemical pharmacology, 2020-09, Vol.179, p.113930-113930, Article 113930

2020

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5-Oxo-ETE and the OXE receptor

Prostaglandins & other lipid mediators, 2009-09, Vol.89 (3), p.98-104

2009

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Concise Syntheses of Microsomal Metabolites of a Potent OXE (Oxoeicosanoid) Receptor Antagonist

Chemical and Pharmaceutical Bulletin, 2023/07/01, Vol.71(7), pp.534-544

2023

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Ligand-controlled switch in diastereoselectivities: catalytic asymmetric construction of spirocyclic pyrrolidine-azetidine/oxe(thie)tane derivatives

Chemical communications (Cambridge, England), 2019-06, Vol.55 (51), p.7346-7349

2019

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Biological Roles of 5-Oxo-6,8,11,14-Eicosatetraenoic Acid and the OXE Receptor in Allergic Diseases: Collegium Internationale Allergologicum Update 2024

International archives of allergy and immunology, 2024, Vol.185 (4), p.301-310

2024

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Metabolism of anti-inflammatory OXE (oxoeicosanoid) receptor antagonists by nonhuman primates

European journal of pharmaceutical sciences, 2022-05, Vol.172, p.106144-106144, Article 106144

2022

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First Report of Diaporthe oxe on Peroba Rosa in Brazil

Plant disease, 2020-06, Vol.104 (6), p.1861-1861

2020

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Novel highly potent OXE receptor antagonists with prolonged plasma lifetimes that are converted to active metabolites in vivo in monkeys

British journal of pharmacology, 2020-01, Vol.177 (2), p.388-401

2020

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In vivo α-hydroxylation of a 2-alkylindole antagonist of the OXE receptor for the eosinophil chemoattractant 5-oxo-6,8,11,14-eicosatetraenoic acid in monkeys

Biochemical pharmacology, 2017-08, Vol.138, p.107-118

2017

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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)

Journal of medicinal chemistry, 2018-07, Vol.61 (14), p.5934-5948

2018

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Pharmacokinetics and Metabolism of Selective Oxoeicosanoid (OXE) Receptor Antagonists and Their Effects on 5‑Oxo-6,8,11,14-eicosatetraenoic Acid (5-Oxo-ETE)-Induced Granulocyte Activation in Monkeys

Journal of medicinal chemistry, 2016-11, Vol.59 (22), p.10127-10146

2016

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A biased ligand for OXE-R uncouples Gα and Gβγ signaling within a heterotrimer

Nature chemical biology, 2012-07, Vol.8 (7), p.631-638

2012

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Two Potent OXE‑R Antagonists: Assignment of Stereochemistry

ACS medicinal chemistry letters, 2014-07, Vol.5 (7), p.815-819

2014

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Corrigendum to “In vivo α-hydroxylation of a 2-alkylindole antagonist of the OXE receptor for the eosinophil chemoattractant 5-oxo-6,8,11,14-eicosatetraenoic acid in monkeys” [Biochem. Pharmacol. 138 (2017) 107–118]

Biochemical pharmacology, 2018-08, Vol.154, p.174-174

2018

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Metabolism and pharmacokinetics of a potent N-acylindole antagonist of the OXE receptor for the eosinophil chemoattractant 5-oxo-6,8,11,14-eicosatetraenoic acid (5-oxo-ETE) in rats and monkeys

European journal of pharmaceutical sciences, 2018-03, Vol.115, p.88-99

2018

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Ahô-ô-ô-oxe, by Ribeiro Neto

Matraga, 2018-08, Vol.25 (43), p.236-239

Leonardo Davino de Oliveira

2018

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Expression and function of OXE receptor, an eicosanoid receptor, in steroidogenic cells

Molecular and cellular endocrinology, 2013-05, Vol.371 (1-2), p.71-78

2013

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RIBEIRO NETO, Amador. Ahô-ô-ô-oxe

Matraga, 2018-06, Vol.25 (43)

De Oliveira, Leonardo Davino

2018

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In vivo α-hydroxylation of a 2-alkylindole antagonist of the OXE receptor for the eosinophil chemoattractant 5-oxo-6,8,11,14-eicosatetraenoic acid in monkeys1

Biochemical pharmacology, 2017-05, Vol.138, p.107-118

2017

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On the nature of interactions in the F 2 OXe … NCCH 3 complex: Is there the Xe(IV)N bond?

Journal of computational chemistry, 2016-07, Vol.37 (20), p.1876-1886

2016

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Self-healing inside a scratch of oxetane-substituted chitosan-polyurethane (OXE-CHI-PUR) networks

Journal of materials chemistry, 2011-01, Vol.21 (38), p.14473-14486

2011

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On the nature of interactions in the F^sub 2^OXe...NCCH^sub 3^ complex: Is there the Xe(IV) - N bond?

Journal of computational chemistry, 2016-07, Vol.37 (20), p.1876

2016

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Optimal synthetic conditions for oxetane-substituted chitosan (OXE-CHI) and polyethylene glycol (PEG) network self-healing agent

Materials express, 2017-10, Vol.7 (5), p.411-416

2017

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Targeting the OXE receptor with a selective antagonist inhibits allergen‐induced pulmonary inflammation in non‐human primates

The eosinophil chemoattractant 5-oxo-ETE and the OXE receptor

Targeting the OXE receptor as a potential novel therapy for asthma

5-Oxo-ETE and the OXE receptor

Concise Syntheses of Microsomal Metabolites of a Potent OXE (Oxoeicosanoid) Receptor Antagonist

Ligand-controlled switch in diastereoselectivities: catalytic asymmetric construction of spirocyclic pyrrolidine-azetidine/oxe(thie)tane derivatives

Biological Roles of 5-Oxo-6,8,11,14-Eicosatetraenoic Acid and the OXE Receptor in Allergic Diseases: Collegium Internationale Allergologicum Update 2024

Metabolism of anti-inflammatory OXE (oxoeicosanoid) receptor antagonists by nonhuman primates

First Report of Diaporthe oxe on Peroba Rosa in Brazil

Novel highly potent OXE receptor antagonists with prolonged plasma lifetimes that are converted to active metabolites in vivo in monkeys

In vivo α-hydroxylation of a 2-alkylindole antagonist of the OXE receptor for the eosinophil chemoattractant 5-oxo-6,8,11,14-eicosatetraenoic acid in monkeys

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)

Pharmacokinetics and Metabolism of Selective Oxoeicosanoid (OXE) Receptor Antagonists and Their Effects on 5‑Oxo-6,8,11,14-eicosatetraenoic Acid (5-Oxo-ETE)-Induced Granulocyte Activation in Monkeys

A biased ligand for OXE-R uncouples Gα and Gβγ signaling within a heterotrimer

Two Potent OXE‑R Antagonists: Assignment of Stereochemistry

Corrigendum to “In vivo α-hydroxylation of a 2-alkylindole antagonist of the OXE receptor for the eosinophil chemoattractant 5-oxo-6,8,11,14-eicosatetraenoic acid in monkeys” [Biochem. Pharmacol. 138 (2017) 107–118]

Metabolism and pharmacokinetics of a potent N-acylindole antagonist of the OXE receptor for the eosinophil chemoattractant 5-oxo-6,8,11,14-eicosatetraenoic acid (5-oxo-ETE) in rats and monkeys

Ahô-ô-ô-oxe, by Ribeiro Neto

Expression and function of OXE receptor, an eicosanoid receptor, in steroidogenic cells

RIBEIRO NETO, Amador. Ahô-ô-ô-oxe

In vivo α-hydroxylation of a 2-alkylindole antagonist of the OXE receptor for the eosinophil chemoattractant 5-oxo-6,8,11,14-eicosatetraenoic acid in monkeys1

On the nature of interactions in the F 2 OXe … NCCH 3 complex: Is there the Xe(IV)N bond?

Self-healing inside a scratch of oxetane-substituted chitosan-polyurethane (OXE-CHI-PUR) networks

On the nature of interactions in the F^sub 2^OXe...NCCH^sub 3^ complex: Is there the Xe(IV) - N bond?

Optimal synthetic conditions for oxetane-substituted chitosan (OXE-CHI) and polyethylene glycol (PEG) network self-healing agent

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