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Selective noradrenalin re-uptake inhibitor.
|Storage||Store at RT|
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.
|Solvent||Max Conc. mg/mL||Max Conc. mM|
Preparing Stock Solutions
The following data is based on the product molecular weight 313.87. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
|Concentration / Solvent Volume / Mass||1 mg||5 mg||10 mg|
|0.1 mM||31.86 mL||159.3 mL||318.6 mL|
|0.5 mM||6.37 mL||31.86 mL||63.72 mL|
|1 mM||3.19 mL||15.93 mL||31.86 mL|
|5 mM||0.64 mL||3.19 mL||6.37 mL|
References are publications that support the biological activity of the product.
Pawlowski and Nowak (1987) Biochemical and pharmacological tests for the prediction of ability of monoamine uptake blockers to inhibit the uptake of noradrenaline in-vivo: the effects of desipramine, maprotiline, femoxetine and cital. J.Pharm.Pharmacol. 39 1003 PMID: 2894425
Pinder et al (1977) Maprotiline: A review of its pharmacological properties and therapeutic efficacy in mental depressive states. Drugs 13 321 PMID: 326531
Rodgers et al (1997) Behavioural effects in mice of subchronic chlordiazepoxide, maprot. and fluvox. II. The elevated plus-maze. Pharmacol.Biochem.Behav. 57 127 PMID: 9164563
Merck Index 11 5633
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Citations for Maprotiline hydrochloride
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