Citalopram hydrobromide
Chemical Name: 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-5-isobenzofurancarbonitrile hydrobromide
Purity: ≥99%
Biological Activity
Citalopram hydrobromide is a highly selective and potent 5-HT uptake inhibitor with no effect on noradrenalin or dopamine uptake (IC50 values are 1.8, 8800 and 41000 nM respectively). Has negligible activity at a wide range of receptors.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Additional Information
Background References
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Olanzapine: preclinical and clinical profiles of a novel antipsychotic agent.
Tollefson and Taylor
CNS Drug Reviews, 2000;6:303 -
Effect of chronic administration of the selective serotonin (5-HT) uptake inhibitor citalopram on extracellular 5-HT and apparent autoreceptor sensitivity in rat forebrain in vivo.
Auerbach and Hjorth
Naunyn Schmiedebergs Arch.Pharmacol., 1995;352:597 -
Inhibition of 5-hydroxytryptamine reuptake by the antidepressant citalopram in the locus coeruleus modulates the rat brain noradrenergic transmission in vivo.
Mateo et al.
Neuropharmacology, 2000;39:2036 -
Citalopram - pharmacological profile of a specific serotonin uptake inhibitor with antidepressant activity.
Hyttel
Prog.Drug Metabolism. Eds. Bridges, J. W. & Ch, 1982;6:277 -
Effect of chronic administration of the selective serotonin (5-HT) uptake inhibitor cital. on extracellular 5-HT and apparent autoreceptor sensitivity in rat forebrain in vivo.
Auerbach and Hjorth
Naunyn Schmiedebergs Arch.Pharmacol., 1995;352:597 -
Inhibition of 5-hydroxytryptamine reuptake by the antidepressant cital. in the locus coeruleus modulates the rat brain noradrenergic transmission in vivo.
Mateo et al.
Neuropharmacology, 2000;39:2036
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Citations for Citalopram hydrobromide
The citations listed below are publications that use Tocris products. Selected citations for Citalopram hydrobromide include:
14 Citations: Showing 1 - 10
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Cocaine Inhibition of Synaptic Transmission in the Ventral Pallidum Is Pathway-Specific and Mediated by Serotonin.
Authors: Matsui and Alvarez
Cell Rep 2018;23(13):3852
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Serotonergic mechanisms involved in antidepressant-like responses evoked by GLT-1 blockade in rat infralimbic cortex.
Authors: Gasull-Camôs Et al.
Neuropharmacology 2018;139:41
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Psychopharmacological characterisation of the successive negative contrast effect in rats.
Authors: Phelps Et al.
Mol Ther 2015;232:2697
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Brain Histamine Is Crucial for Selective Serotonin Reuptake Inhibitors' Behavioral and Neurochemical Effects.
Authors: Munari Et al.
Psychopharmacology (Berl) 2015;18:pyv045
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Enhanced responsiveness to selective serotonin reuptake inhibitors during lactation.
Authors: Jury Et al.
PLoS One 2015;10:e0117339
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Discovery of novel-scaffold monoamine transporter ligands via in silico screening with the S1 pocket of the serotonin transporter.
Authors: Nolan Et al.
ACS Chem Neurosci 2014;5:784
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The role of GluN2A and GluN2B subunits on the effects of NMDA receptor antagonists in modeling schizophrenia and treating refractory depression.
Authors: Jiménez-Sánchez Et al.
Neuropsychopharmacology 2014;39:2673
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A translational rodent assay of affective biases in depression and antidepressant therapy.
Authors: Stuart Et al.
Neuropsychopharmacology 2013;38:1625
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Differential regulation of MeCP2 phosphorylation in the CNS by DA and serotonin.
Authors: Hutchinson Et al.
Cardiovasc Res 2012;37:321
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Gene therapy by targeted adenovirus-mediated knockdown of pulmonary endothelial Tph1 attenuates hypoxia-induced pulmonary hypertension.
Authors: Morecroft Et al.
PLoS One 2012;20:1516
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In vivo effects of a combined 5-HT1B receptor/SERT antagonist in experimental pulmonary hypertension.
Authors: Morecroft Et al.
Int J Neuropsychopharmacol 2010;85:593
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Recovery of motoneuron and locomotor function after spinal cord injury depends on constitutive activity in 5-HT2C receptors.
Authors: Murray Et al.
Nat Med 2010;16:694
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Neonatal antidepressant exposure has lasting effects on behavior and serotonin circuitry.
Authors: Maciag Et al.
Neuropsychopharmacology 2006;31:47
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Evidence that the deficit in sexual behavior in adult rats neonatally exposed to cital. is a consequence of 5-HT1 receptor stimulation during development.
Authors: Maciag Et al.
Brain Res 2006;1125:171
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