Related references
Note: Only part of the references are listed.Development of VU6019650: A Potent, Highly Selective, andSystemically Active Orthosteric Antagonist of the M5MuscarinicAcetylcholine Receptor for the Treatment of Opioid Use Disorder
Aaron T. Garrison et al.
JOURNAL OF MEDICINAL CHEMISTRY (2022)
Examining the role of muscarinic M5 receptors in VTA cholinergic modulation of depressive-like and anxiety-related behaviors in rats
Eric J. Nunes et al.
NEUROPHARMACOLOGY (2020)
Acute Negative Allosteric Modulation of M5 Muscarinic Acetylcholine Receptors Inhibits Oxycodone Self-Administration and Cue-Induced Reactivity with No Effect on Antinociception
Robert W. Gould et al.
ACS CHEMICAL NEUROSCIENCE (2019)
Crystal structure of the M5 muscarinic acetylcholine receptor
Ziva Vuckovic et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2019)
Muscarinic M5 receptors modulate ethanol seeking in rats
Alice E. Berizzi et al.
NEUROPSYCHOPHARMACOLOGY (2018)
Molecular Mechanisms of Action of M5 Muscarinic Acetylcholine Receptor Allosteric Modulators
Alice E. Berizzi et al.
MOLECULAR PHARMACOLOGY (2016)
M5 Receptor Activation Produces Opposing Physiological Outcomes in Dopamine Neurons Depending on the Receptor's Location
Daniel J. Foster et al.
JOURNAL OF NEUROSCIENCE (2014)
Structural Modifications to Tetrahydropyridine-3-carboxylate Esters en Route to the Discovery of M5-Preferring Muscarinic Receptor Orthosteric Antagonists
Guangrong Zheng et al.
JOURNAL OF MEDICINAL CHEMISTRY (2013)
Muscarinic Acetylcholine Receptor Subtypes as Potential Drug Targets for the Treatment of Schizophrenia, Drug Abuse, and Parkinson's Disease
Ditte Dencker et al.
ACS CHEMICAL NEUROSCIENCE (2012)
Reduced cocaine self-administration in muscarinic M5 acetylcholine receptor-deficient mice
M Thomsen et al.
JOURNAL OF NEUROSCIENCE (2005)
Role for M5 muscarinic acetylcholine receptors in cocaine addiction
A Fink-Jensen et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2003)
Deletion of the M5 muscarinic acetylcholine receptor attenuates morphine reinforcement and withdrawal but not morphine analgesia
AS Basile et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)