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Crystal Structure of the Human Cannabinoid Receptor CB1

Cell, 2016-10, Vol.167 (3), p.750-762.e14

2016

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Activation and Signaling Mechanism Revealed by Cannabinoid Receptor-Gi Complex Structures

Cell, 2020-02, Vol.180 (4), p.655-665.e18

2020

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Biased agonists of the kappa opioid receptor suppress pain and itch without causing sedation or dysphoria

Science signaling, 2016-11, Vol.9 (456), p.ra117

2016

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Low Intrinsic Efficacy Alone Cannot Explain the Improved Side Effect Profiles of New Opioid Agonists

Biochemistry (Easton), 2022-09, Vol.61 (18), p.1923-1935

2022

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Hyperactivity in Mice Induced by Opioid Agonists with Partial Intrinsic Efficacy and Biased Agonism Administered Alone and in Combination with Morphine

Biomolecules (Basel, Switzerland), 2023-06, Vol.13 (6), p.935

2023

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A Route to Potent, Selective, and Biased Salvinorin Chemical Space

ACS central science, 2023-08, Vol.9 (8), p.1567-1574

2023

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A novel method for analyzing extremely biased agonism at G protein-coupled receptors

Molecular pharmacology, 2015-05, Vol.87 (5), p.866-877

2015

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Decaf or regular? Energizing the caffeine receptor

Cell, 2021-04, Vol.184 (7), p.1659-1660

2021

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G protein signaling-biased mu opioid receptor agonists that produce sustained G protein activation are noncompetitive agonists

Proceedings of the National Academy of Sciences - PNAS, 2021-11, Vol.118 (48)

2021

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A G protein signaling-biased agonist at the μ-opioid receptor reverses morphine tolerance while preventing morphine withdrawal

Neuropsychopharmacology (New York, N.Y.), 2020-01, Vol.45 (2), p.416-425

2020

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Arrestin recruitment to dopamine D2 receptor mediates locomotion but not incentive motivation

Molecular psychiatry, 2020-09, Vol.25 (9), p.2086-2100

2020

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Synthesis and evaluation of 3,4,5-trisubstituted triazoles as G protein-biased kappa opioid receptor agonists

European journal of medicinal chemistry, 2024-10, Vol.276, p.116627, Article 116627

2024

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G protein signaling-biased agonism at the κ-opioid receptor is maintained in striatal neurons

Science signaling, 2018-08, Vol.11 (542)

2018

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Characterization of structurally novel G protein biased CB1 agonists: Implications for drug development

Pharmacological research, 2017-11, Vol.125 (Pt B), p.161-177

2017

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Approaches to Assess Biased Signaling at the CB1R Receptor

Methods in enzymology, 2017, Vol.593, p.259

2017

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Characterization of kappa opioid receptor mediated, dynorphin-stimulated [35S]GTPγS binding in mouse striatum for the evaluation of selective KOR ligands in an endogenous setting

Neuropharmacology, 2015-12, Vol.99, p.131-141

2015

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Probing the CB1 Cannabinoid Receptor Binding Pocket with AM6538, a High-Affinity Irreversible Antagonist

Molecular pharmacology, 2019-11, Vol.96 (5), p.619-628

2019

Volltextzugriff (PDF)

Probing the CB 1 Cannabinoid Receptor Binding Pocket with AM6538, a High-Affinity Irreversible Antagonist

Molecular pharmacology, 2019-11, Vol.96 (5), p.619-628

2019

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Structure–Activity Relationship Studies of Functionally Selective Kappa Opioid Receptor Agonists that Modulate ERK 1/2 Phosphorylation While Preserving G Protein Over βArrestin2 Signaling Bias

ACS chemical neuroscience, 2015-08, Vol.6 (8), p.1411-1419

2015

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Characterization of structurally novel G protein biased CB 1 agonists: Implications for drug development

Pharmacological research, 2017-11, Vol.125 (Pt B), p.161-177

2017

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Correction to “Structure–Activity Relationship Studies of Functionally Selective Kappa Opioid Receptor Agonists that Modulate ERK 1/2 Phosphorylation While Preserving G Protein Over βArrestin2 Signaling Bias”

ACS chemical neuroscience, 2017-07, Vol.8 (7), p.1628-1628

2017

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A G Protein‐Biased Ligand of the Kappa Opioid Receptor is Antinociceptive and Antipruritic But Does Not Cause Sedation or Dysphoria

The FASEB journal, 2017-04, Vol.31 (S1)

2017

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Crystal Structure of the Human Cannabinoid Receptor CB1

Cell, 2016-10, Vol.167 (3)

2016

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Activation and Signaling Mechanism Revealed by Cannabinoid Receptor-G i Complex Structures

Cell, 2020-02, Vol.180 (4), p.655

2020

Volltextzugriff (PDF)

Crystal Structure of the Human Cannabinoid Receptor CB 1

Cell, 2016-10, Vol.167 (3), p.750

2016

Volltextzugriff (PDF)

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Crystal Structure of the Human Cannabinoid Receptor CB1

Activation and Signaling Mechanism Revealed by Cannabinoid Receptor-Gi Complex Structures

Biased agonists of the kappa opioid receptor suppress pain and itch without causing sedation or dysphoria

Low Intrinsic Efficacy Alone Cannot Explain the Improved Side Effect Profiles of New Opioid Agonists

Hyperactivity in Mice Induced by Opioid Agonists with Partial Intrinsic Efficacy and Biased Agonism Administered Alone and in Combination with Morphine

A Route to Potent, Selective, and Biased Salvinorin Chemical Space

A novel method for analyzing extremely biased agonism at G protein-coupled receptors

Decaf or regular? Energizing the caffeine receptor

G protein signaling-biased mu opioid receptor agonists that produce sustained G protein activation are noncompetitive agonists

A G protein signaling-biased agonist at the μ-opioid receptor reverses morphine tolerance while preventing morphine withdrawal

Arrestin recruitment to dopamine D2 receptor mediates locomotion but not incentive motivation

Synthesis and evaluation of 3,4,5-trisubstituted triazoles as G protein-biased kappa opioid receptor agonists

G protein signaling-biased agonism at the κ-opioid receptor is maintained in striatal neurons

Characterization of structurally novel G protein biased CB1 agonists: Implications for drug development

Approaches to Assess Biased Signaling at the CB1R Receptor

Characterization of kappa opioid receptor mediated, dynorphin-stimulated [35S]GTPγS binding in mouse striatum for the evaluation of selective KOR ligands in an endogenous setting

Probing the CB1 Cannabinoid Receptor Binding Pocket with AM6538, a High-Affinity Irreversible Antagonist

Probing the CB 1 Cannabinoid Receptor Binding Pocket with AM6538, a High-Affinity Irreversible Antagonist

Structure–Activity Relationship Studies of Functionally Selective Kappa Opioid Receptor Agonists that Modulate ERK 1/2 Phosphorylation While Preserving G Protein Over βArrestin2 Signaling Bias

Characterization of structurally novel G protein biased CB 1 agonists: Implications for drug development

Correction to “Structure–Activity Relationship Studies of Functionally Selective Kappa Opioid Receptor Agonists that Modulate ERK 1/2 Phosphorylation While Preserving G Protein Over βArrestin2 Signaling Bias”

A G Protein‐Biased Ligand of the Kappa Opioid Receptor is Antinociceptive and Antipruritic But Does Not Cause Sedation or Dysphoria

Crystal Structure of the Human Cannabinoid Receptor CB1

Activation and Signaling Mechanism Revealed by Cannabinoid Receptor-G i Complex Structures

Crystal Structure of the Human Cannabinoid Receptor CB 1

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