(S)-Duloxetine hydrochloride
Chemical Name: (+)-(S)-N-Methyl-3-(1-naphthyloxy)-3-(2-thienyl)propanamine hydrochloride
Purity: ≥99%
Biological Activity
(S)-Duloxetine hydrochloride is a high affinity, competitive 5-HT and noradrenaline (NA) re-uptake inhibitor (Ki values are 8.5 and 45 nM for 5-HT and NA reuptake respectively in cortical synaptosomes; IC50 values are 28 and 46 nM for 5-HT and NA reuptake respectively in rat hippocampal slices). Also blocks dopamine reuptake (Ki = 300 nM in striatal synaptosomes). Exhibits antidepressant and anxiolytic effects. Orally bioavailable.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.
Background References
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LY227942, an inhibitor of serotonin and NE uptake: biochemical pharmacology of a potential antidepressant drug.
Wong et al.
Life Sci., 1988;43:2049 -
Blockade of the serotonin and NE uptake processes by duloxetine: in vitro and in vivo studies in the rat brain.
Kasamo et al.
J.Pharmacol.Exp.Ther., 1996;277:278
Product Datasheets
Citations for (S)-Duloxetine hydrochloride
The citations listed below are publications that use Tocris products. Selected citations for (S)-Duloxetine hydrochloride include:
4 Citations: Showing 1 - 4
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Mitochondrial and Neuronal Dysfunctions in L1 Mutant Mice.
Authors: Melitta Et al.
Int J Mol Sci 2022;23
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Directed Evolution of a Selective and Sensitive Serotonin Sensor via Machine Learning.
Authors: Henry A Et al.
Cell 2020;183:1986-2002.e26
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Effect of monoamine reuptake inhibition and α1 blockade on respiratory arrest and death following electroshock-induced seizures in mice.
Authors: Gordon F Et al.
Epilepsia 2019;60:495-507
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Chronic treatment with pra. or dulox. lessens concurrent anxiety-like behavior and alcohol intake: evidence of disrupted noradrenergic signaling in anxiety-related alcohol use.
Authors: Skelly and Weiner
Brain Behav 2014;4:468
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