Search Results - "Ross, Nicolette C."
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Bias Factor and Therapeutic Window Correlate to Predict Safer Opioid Analgesics
Published in Cell (16-11-2017)“…Biased agonism has been proposed as a means to separate desirable and adverse drug responses downstream of G protein-coupled receptor (GPCR) targets. Herein,…”
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Reactive Oxygen and Targeted Antioxidant Administration in Endothelial Cell Mitochondria
Published in The Journal of biological chemistry (29-12-2006)“…We used fluorescent probes and EPR to study the mechanism(s) underlying reactive oxygen species (ROS) production by endothelial cell mitochondria and the…”
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Mitochondrial targeted coenzyme Q, superoxide, and fuel selectivity in endothelial cells
Published in PloS one (22-01-2009)“…Previously, we reported that the "antioxidant" compound "mitoQ" (mitochondrial-targeted ubiquinol/ubiquinone) actually increased superoxide production by…”
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Optimization of a Series of Mu Opioid Receptor (MOR) Agonists with High G Protein Signaling Bias
Published in Journal of medicinal chemistry (11-10-2018)“…While mu opioid receptor (MOR) agonists are especially effective as broad-spectrum pain relievers, it has been exceptionally difficult to achieve a clear…”
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Physical presence of nor-binaltorphimine in mouse brain over 21 days after a single administration corresponds to its long-lasting antagonistic effect on κ-opioid receptors
Published in The Journal of pharmacology and experimental therapeutics (01-09-2013)“…In the mouse 55°C warm-water tail-withdrawal assay, a single administration of nor-binaltorphimine (nor-BNI; 10 mg/kg i.p.) antagonized κ-opioid receptor (KOR)…”
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Novel opioid cyclic tetrapeptides: Trp isomers of CJ‐15,208 exhibit distinct opioid receptor agonism and short‐acting κ opioid receptor antagonism
Published in British journal of pharmacology (01-02-2012)“…BACKGROUND AND PURPOSE The κ opioid receptor antagonists demonstrate potential for maintaining abstinence from psychostimulant abuse, but existing non‐peptide…”
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The Macrocyclic Peptide Natural Product CJ-15,208 Is Orally Active and Prevents Reinstatement of Extinguished Cocaine-Seeking Behavior
Published in Journal of natural products (Washington, D.C.) (22-03-2013)“…The macrocyclic tetrapeptide natural product CJ-15,208 (cyclo[Phe-d-Pro-Phe-Trp]) exhibited both dose-dependent antinociception and kappa opioid receptor (KOR)…”
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Synthesis of CJ-15,208, a novel κ-opioid receptor antagonist
Published in Tetrahedron letters (20-09-2010)“…A strategy to select linear precursor peptides favoring cyclization was developed and cyclization conditions were optimized. The tryptophan isomers of the…”
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Unexpected Opioid Activity Profiles of Analogues of the Novel Peptide Kappa Opioid Receptor Ligand CJ-15,208
Published in ChemMedChem (05-09-2011)“…An alanine scan was performed on the novel κ opioid receptor (KOR) peptide ligand CJ‐15,208 to determine which residues contribute to the potent in vivo…”
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Synthesis of cyclic tetrapeptide CJ 15,208: a novel kappa opioid receptor antagonist
Published in Advances in experimental medicine and biology (2009)Get more information
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Mu Opioid Receptor Agonists with Dopamine D3 Receptor Antagonism: Toward Developing Analgesics with Less Abuse Potential
Published in The FASEB journal (01-04-2018)“…Opioid analgesics such as morphine are widely used in clinical practice for the management of moderate to severe pain. While they are the gold standard for…”
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Novel opioid cyclic tetrapeptides: Trp isomers of CJ-15,208 exhibit distinct opioid receptor agonism and short-acting [kappa] opioid receptor antagonism
Published in British journal of pharmacology (01-02-2012)“…BACKGROUND AND PURPOSE The [kappa] opioid receptor antagonists demonstrate potential for maintaining abstinence from psychostimulant abuse, but existing…”
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The Macrocyclic Peptide Natural Product CJ-15,208 is Orally Active and Prevents Reinstatement of Extinguished Cocaine Seeking Behavior1
Published in Journal of natural products (Washington, D.C.) (17-01-2013)“…The macrocyclic tetrapeptide natural product CJ-15,208 ( cyclo [Phe-D-Pro-Phe-Trp]) exhibited both dose-dependent antinociception and kappa opioid receptor…”
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