Search Results - "Le Naour, Morgan"
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1
Bivalent Ligands That Target μ Opioid (MOP) and Cannabinoid1 (CB1) Receptors Are Potent Analgesics Devoid of Tolerance
Published in Journal of medicinal chemistry (11-07-2013)“…Given that μ opioid (MOP) and canabinoid (CB1) receptors are colocalized in various regions of the central nervous system and have been reported to associate…”
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2
Putative Kappa Opioid Heteromers As Targets for Developing Analgesics Free of Adverse Effects
Published in Journal of medicinal chemistry (14-08-2014)“…It is now generally recognized that upon activation by an agonist, β-arrestin associates with G protein-coupled receptors and acts as a scaffold in creating a…”
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3
Effect of 6-Benzoyl-benzothiazol-2-one scaffold on the pharmacological profile of α-alkoxyphenylpropionic acid derived PPAR agonists
Published in Journal of enzyme inhibition and medicinal chemistry (01-01-2020)“…A series of nitrogen heterocycles containing α-ethoxyphenylpropionic acid derivatives were designed as dual PPARα/γ agonist ligands for the treatment of type 2…”
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4
Effect of Oxime Ether Incorporation in Acyl Indole Derivatives on PPAR Subtype Selectivity
Published in ChemMedChem (01-12-2012)“…Compounds that simultaneously activate peroxisome proliferator‐activated receptor (PPAR) subtypes α and γ have the potential to effectively treat dyslipidemia…”
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5
A Fentanyl Vaccine Alters Fentanyl Distribution and Protects against Fentanyl-Induced Effects in Mice and Rats
Published in The Journal of pharmacology and experimental therapeutics (01-02-2019)“…Fentanyl is an extremely potent synthetic opioid that has been increasingly used to adulterate heroin, cocaine, and counterfeit prescription pills, leading to…”
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Reduced Antinociception of Opioids in Rats and Mice by Vaccination with Immunogens Containing Oxycodone and Hydrocodone Haptens
Published in Journal of medicinal chemistry (14-02-2013)“…Prescription opioids abuse and associated deaths are an emerging concern in the USA. Vaccination against prescription opioids may provide an alternative to…”
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7
Opioid Activity of Spinally Selective Analogues of N-Naphthoyl-β-naltrexamine in HEK-293 Cells and Mice
Published in Journal of medicinal chemistry (26-01-2012)“…Using the selective mu–kappa agonist, N-naphthoyl-β-naltrexamine 1, as the prototype ligand, a series of closely related naphthalene analogues were synthesized…”
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