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Talopram (hydrochloride)

Talopram hydrochloride is a selective inhibitor for norepinephrine transporter (NET), that inhibits 63% human NET at 100 nM[1].

Product Specifications

CAS Number

7013-41-4

UNSPSC

12352005

Hazard Statement

H302

Target

Monoamine Transporter

Type

Reference compound

Related Pathways

Membrane Transporter/Ion Channel

Applications

Neuroscience-Neuromodulation

Field of Research

Neurological Disease

Assay Protocol

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

Smiles

CC1(C)OC(CCCNC)(C2=CC=CC=C2)C3=C1C=CC=C3.Cl

Molecular Formula

C20H26ClNO

Molecular Weight

331.88

Precautions

P264-P270-P330-P501

References & Citations

[1]Eildal JN, et al., From the selective serotonin transporter inhibitor citalopram to the selective norepinephrine transporter inhibitor talopram: synthesis and structure-activity relationship studies. J Med Chem. 2008 May 22;51 (10) :3045-8.

Shipping Conditions

Room temperature

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Frequently Asked Questions

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