Description: Potent, selective inhibitor of noradrenalin transporters
Alternative Names: Lu 3-010
Chemical Name: 1,3-Dihydro-N,3,3-trimethyl-1-phenyl-1-isobenzofuranpropanamine hydrochloride
Purity: ≥99% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Potent, selective inhibitor of the noradrenalin transporter (NET) (IC50 = 2.9 nM). Exhibits selectivity for NET against SERT (5-HT transporters) and DAT (dopamine transporters). Displays a similar structure but different pharmacological profile to citalopram (Cat. No. 1427).
Compound Libraries
Talopram hydrochloride is also offered as part of the
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Technical Data
M. Wt
331.88
Formula
C20H25NO.HCl
Storage
Desiccate at RT
Purity
≥99% (HPLC)
CAS Number
7013-41-4
PubChem ID
71176
InChI Key
JZXJIRQPHHWYGC-UHFFFAOYSA-N
Smiles
CC2(C)OC(C3=CC=CC=C3)(CCCNC)C1=CC=CC=C12.Cl
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent
Max Conc. mg/mL
Max Conc. mM
Solubility
DMSO
33.19
100
ethanol
33.19
100
water
16.59
50
Preparing Stock Solutions
The following data is based on the product molecular weight 331.88. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
3.01 mL
15.07 mL
30.13 mL
5 mM
0.6 mL
3.01 mL
6.03 mL
10 mM
0.3 mL
1.51 mL
3.01 mL
50 mM
0.06 mL
0.3 mL
0.6 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products' biological activity.
Bogesoet al (1985) 3-phenyl-1-indanamines. Potential antidepressant activity and potent inhibition of dopamine, norepinephrine, and serotonin uptake. J.Med.Chem. 28 1817 PMID: 2999402
Eildalet al (2008) From the selective serotonin transporter inhibitor citalopram to the selective norepinephrine transporter inhibitor talopram: synthesis and structure-activity relationship studies. J.Med.Chem. 51 3045 PMID: 18429609
Schouet al (2006) Synthesis and positron emission tomography evaluation of three norepinephrine transporter radioligands: [C-11]desipramine, [C-11]talopram and [C-11]talsupram. Mol.Imaging Biol. 8 1 PMID: