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Product Details

Product introduction：

Cas: 66981-73-5

Appearance: White or almost white microcrystalline powder

MF: C₂₃H₂₉ClN₂O₄S

Overview: Product description:
Tianeptine is a drug used for treating major depressive episodes (mild, moderate, or severe). It has structural similarities to the tricyclic antidepressants, but it has different pharmacological properties. Tianeptine is a selective serotonin reuptake enhancer (SSRE), opposite to the action of SSRIs. One review points to the cancellative effects of tianeptine and fluoxetine coadministration on serotonin reuptake. Another suggests that long-term administration of tianeptine has no effect on serotonin pathways. Tianeptine enhances the extracellular concentration of dopamine in the nucleus accumbens and modulates the D2 and D3 dopamine receptors. There is also action on the NMDA and AMPA receptors.
Tianeptine also known as stablon, is a drug primarily used in the treatment of Major depressive disorder. It has also been used to treat irritable bowel syndrome and asthma. Tianeptine has antidepressant and anti-anxiety properties.

Tianeptine has a variety of effects on the body, including motivation enhancement, anxiety suppression, cognitive euphoria, focus enhancement, rejuvenation, and cognitive fatigu.

Associated Conditions: Major Depressive Disorder (MDD)

Application: Tia free acid is tricyclic antidepressants that have antidepressant effects by acting on the serotonin system. In animal experiments, they can increase the spontaneous activity of pyramidal cells in the hippocampus and accelerate their recovery after inhibition of function. It can increase the reabsorption of serotonin by neurons in the cerebral cortex and hippocampus

Other chemical names: Coaxil, Stablon,

7-[(3-chloro-6,11-dihydro-6-methyldibenzo[c,f][1,2]thiazepin-11-yl)-amino]heptanoic acid s,s-dioxide

Certificate of analysia

TEST ITEM	SPECIFICATION	RESULT
Appearance	White or almost white microcrystalline powder	White powder
Solubility	Insoluble in the water and methanol	Complies
Identification	Should comply	Complies
Related substance	Individual impurity: Not more than0.1%	0.06%
	Total impurities: Not more than 0.5%	0.13%
Residue on ignation	Not more than 0.2%	0.02%
Loss on drying	Not more than 1.0%	0.09%
Heavy metal	Not more than 20ppm	＜ 20ppm
Assay (on anhydrous basis)	Not less than 99.0%	99.35%
Conclusion : Conform to per enterprise standard

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