Place of Origin: | Shaanxi, China (Mainland) |
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Brand Name: | XABC |
Certification: | ISO9001 |
Model Number: | XABC3056 |
Minimum Order Quantity: | 10g |
Price: | $3.6/g-$4.7/g |
Packaging Details: | 25kg carton drum (32cm*58cm)or 1kg foil bag (10cm*15cm) or by request of clients |
Delivery Time: | 1-3 work days |
Payment Terms: | T/T, L/C, Western Union, MoneyGram |
Supply Ability: | 500kg per Month |
Appearance: | White Powder | Grade: | Medicine Grade |
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Sample: | Avaliable | Purity: | 99% |
Storage: | Cool And Dry | Shelf Life: | 2 YEARS |
Product Name: | Tianeptine Acid Cas 66981-73-5 |
CAS: | 66981-73-5 |
MF : | C21H24ClN2NaO4S |
Grade Standard : | Pharmaceutical grade |
Specification: | 99% |
Appearance: | Off- white to white powder |
All types : | Tianeptine; Tianeptine Sodium; Tianeptine sulfate |
sample: | Available |
Storage: | Stored in cool & dry place Kept away from strong light and heat |
Shelf Life: | 2 years when properly stored |
Tianeptine sodium salt is a salt of Tianeptine. Tianeptine, a tricyclic compound, is a selective facilitator of 5-HT (serotonin; sc-201146) uptake in vitro and in vivo. Additionally, Tianeptine is reported to act as a selective inhibitor of dopamine uptake . Tianeptine does not have a noted effect on monoamine uptake. In a study utilizing purified synaptosomes from rat brain, Tianeptine was reported to enhance serotonin uptake in selective brain regions. Purified synaptosomes were obtained from rats and incubated with tritium-labeled 5-HT and Tianeptine in vitro . The synaptosomes were then analyzed for uptake and release of 5-HT via a liquid scintillation.
Tianeptine Acid has antidepressant and anxiolytic (anti-anxiety) properties with a relative lack of sedative, anticholinergic and cardiovascular adverse effects, thus suggesting it is particularly suitable for use in the elderly and in those following alcohol withdrawal; such persons can be more sensitive to the adverse effects of psychotropic drugs. Recent results indicate possible anticonvulsant (anti-seizure) and analgesic (painkilling) activity of tianeptine via immediate or downstream modulation of adenosine A1 receptors (as the effects could be experimentally blocked by antagonists of this receptor).
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