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Tianeptine sodium salt

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Catalog No. T2402Cas No. 30123-17-2
Alias Tianeptine sodium

Tianeptine sodium salt, a selective serotonin reuptake enhancer (SSRE), is used to treat major depressive episodes.

Tianeptine sodium salt

Tianeptine sodium salt

Copy Product Info
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Purity: 99.82%
Catalog No. T2402Alias Tianeptine sodiumCas No. 30123-17-2
Tianeptine sodium salt, a selective serotonin reuptake enhancer (SSRE), is used to treat major depressive episodes.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$33In StockIn Stock
25 mg$50In StockIn Stock
50 mg$62-In Stock
100 mg$92-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.82%
Color:White
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Product Introduction

Bioactivity
Description
Tianeptine sodium salt, a selective serotonin reuptake enhancer (SSRE), is used to treat major depressive episodes.
In vitro
Tianeptine attenuates behavioral symptoms induced by peripheral, but not central, administration of LPS or IL-1β in rats. It normalizes the scaling ratio of NMDA receptor-mediated to AMPA/kainate receptor-mediated current amplitudes and prevents the stress-induced reduction in NMDA-EPSC inactivation. Tianeptine treatment prevents the increase in corticotropin-releasing factor (CRF) mRNA levels in the dBNST triggered by CMS and reduces CRF mRNA levels in the dBNST of non-stressed rats. In anesthetized rats, Tianeptine blocks stress-induced PB inhibition in the basolateral amygdala's CA1 region without affecting stress-induced LTP enhancement. Tianeptine administration under non-stress conditions enhances PB in the amygdala, hippocampus, and LTP in anesthetized rats. Tianeptine significantly decreases cell apoptosis in the rat temporal cortex and hippocampal dentate gyrus in both control and stressed animals but does not affect the Ammons horn. It notably increases extracellular concentrations of homovanillic acid and vanilmandelic acid in the nucleus accumbens and striatum. Intraperitoneal injection of 2.5 mg/kg Tianeptine in the nucleus accumbens alone increases extracellular dopamine.
SynonymsTianeptine sodium
Chemical Properties
Molecular Weight458.93
FormulaC21H24ClN2NaO4S
Cas No.30123-17-2
SmilesCN1c2ccccc2C(c2c(S1(=O)=O)cc(cc2)Cl)NCCCCCCC(=O)[O-].[Na+]
Relative Density.1.38 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: 45.9 mg/mL (100.02 mM), Sonication is recommended.
DMSO: 4.6 mg/mL (10.02 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 1 mg/mL (2.18 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO/H2O
1mg5mg10mg50mg
1 mM2.1790 mL10.8949 mL21.7898 mL108.9491 mL
5 mM0.4358 mL2.1790 mL4.3580 mL21.7898 mL
10 mM0.2179 mL1.0895 mL2.1790 mL10.8949 mL
H2O
1mg5mg10mg50mg
20 mM0.1089 mL0.5447 mL1.0895 mL5.4475 mL
50 mM0.0436 mL0.2179 mL0.4358 mL2.1790 mL
100 mM0.0218 mL0.1089 mL0.2179 mL1.0895 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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