Chemical Name: 2-(Acetyloxy)-N,N,N-trimethylethanaminium chloride
Biological ActivityEndogenous neurotransmitter. Acts at nicotinic and muscarinic acetylcholine receptors.
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Tocris products are intended for laboratory research use only, unless stated otherwise.
The cholinergic 'pitfall': acetylcholine, a universal cell molecule in biological systems, including humans.
Wessler et al.
Citations for Acetylcholine chloride
The citations listed below are publications that use Tocris products. Selected citations for Acetylcholine chloride include:
5 Citations: Showing 1 - 5
Basal Forebrain Cholinergic-induced Activation of Cholecystokinin Inhibitory Neurons in the Basolateral Amygdala.
Authors: Lee and Kim
Exp Neurobiol 2019;28:320
Improved adductor function after canine recurrent laryngeal nerve injury and repair using muscle progenitor cells.
Authors: Paniello Et al.
Stem cell-derived tissue-engineered constructs for hemilaryngeal reconstruction.
Authors: Halum Et al.
Ann Otol Rhinol Laryngol 2014;123:124
Membrane potential measurements of isolated neurons using a voltage-sensitive dye.
Authors: Fairless Et al.
PLoS One 2013;8:e58260
Label-free cell phenotypic assessment of the biased agonism and efficacy of agonists at the endogenous muscarinic M3 receptors.
Authors: Deng Et al.
J Pharmacol Toxicol Methods 2013;68:323
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C57BL6 mice were administered with LPS (5 mg/kg) alone or in combination with Empagliflozin (1 µM) for 16 h. Afterwards mice were sacrificed and aortic rings were isolated. Norepinephrine pre-contracted rings were incubated with indicated (in Image) concentrations of Acetylcholine chloride (ACh) to follow endothelial relaxation.
We used it as an analytical standard for quantification of acetylcholine in brain tissue.