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Doxepin (Hydrochloride)

Doxepin hydrochloride is an orally active tricyclic antidepressant agent. Doxepin hydrochloride is a potent and selective histamine receptor H1 antagonist. Doxepin hydrochloride is also a potent CYP450 inhibitor and significantly inhibits CYP450 2C19 and 1A2[1][2]. Doxepin inhibits reuptake of serotonin and norepinephrine as a tricyclic antidepressant[3].. Doxepin has therapeutic effects in atopic dermatitis, chronic urticarial, can improve cognitive processes, protect central nervous system[4].. Doxepin has also been proposed as a protective factor against oxidative stress[5]..

Product Specifications

CAS Number

[1229-29-4]

UNSPSC

12352005

Hazard Statement

H301, H361

Target

Cytochrome P450; Histamine Receptor

Type

Reference compound

Related Pathways

GPCR/G Protein; Immunology/Inflammation; Metabolic Enzyme/Protease; Neuronal Signaling

Applications

Neuroscience-Neuromodulation

Field of Research

Neurological Disease; Cancer

Assay Protocol

https://www.medchemexpress.com/doxepin-hydrochloride.html

Purity

99.84

Solubility

DMSO : ≥ 100 mg/mL|H2O : ≥ 50 mg/mL

Smiles

CN(C)CC/C=C1C2=CC=CC=C2OCC3=CC=CC=C/13.Cl

Molecular Formula

C19H22ClNO

Molecular Weight

315.84

Precautions

H301, H361

References & Citations

[1]http://pdsp.med.unc.edu/pdsp.php|[2]Hajak, G., et al., Doxepin in the treatment of primary insomnia: a placebo-controlled, double-blind, polysomnographic study. J Clin Psychiatry, 2001. 62 (6) : p. 453-63.|[3]AnnemiekVermeeren, etal. Effects of the use of hypnotics on cognition. Progress in brain research vol. 190 (2011) : 89-103. |[4]G Hajak, etal. Doxepin in the treatment of primary insomnia: a placebo-controlled, double-blind, polysomnographic study. The Journal of clinical psychiatry vol. 62,6 (2001) : 453-63.|[5]Mahsa Gharzi, etal. Effects of different doses of doxepin on passive avoidance learning in rats. Advanced biomedical research vol. 2 66. 30 Jul. 2013.|[6]Jimei Bu, etal. Mechanism underlying the effects of doxepin on β-amyloid -induced memory impairment in rats. Iran J Basic Med Sci. 2017 Sep;20 (9) :1044-1049.

Shipping Conditions

Room Temperature

Storage Conditions

4°C (Powder, sealed storage, away from moisture)

Scientific Category

Reference compound1

Clinical Information

Launched

Isoform

H1 Receptor

Citation 01

Antiviral Res. 2025 Dec:244:106307.|Cell Commun Signal. 2023 May 25;21 (1) :123.|Pharm Res. 2025 Aug;42 (8) :1315-1329.|Virus Res. 2022 Aug:317:198816.|J Appl Toxicol. 2023 Oct;43 (10) :1421-1435.|Nat Commun. 2022 Nov 10;13 (1) :6796.

Available Sizes

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