CAS 30123-17-2 Tianeptine sodium salt Stable Supply

Product Name Tianeptine sodium salt
CAS NO 30123-17-2
Molecular Formula C21H24ClN2NaO4S
Molecular Weight 458.93
Melting point 1800C
Boiling Point 609.2 °C at 760 mmHg
Flash Point 322.2 °C
Density 1.38
Solubility DMSO: ≥20mg/mL
Appearance solid
Storage Desiccate at RT
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CAS 30123-17-2 Tianeptine sodium salt Stable Supply high purity
Product Name Tianeptine sodium salt
Synonyms 7-[(3-chloro-6,11-dihydro-6-methyl-dibenzo[c,f][1,2]thiazepine-11-yl)amino]heptanoic acid s,s dioxide sodium salt; S-1574; 3-Chloro-6,11-dihydro-6-methyl-11-[6-(sodiooxycarbonyl)hexylamino]dibenzo[c,f][1,2]thiazepine 5,5-dioxide; Stablon; [7-[(3-Chloro-6,11-dihydro-6-methyldibenzo[c,f][1,2]thiazepine 5,5-dioxide)-11-ylamino]heptanoic acid]sodium salt;
CAS NO 30123-17-2
Molecular Formula C21H24ClN2NaO4S
Molecular Weight 458.93
Melting point 1800C
Boiling Point 609.2 °C at 760 mmHg
Flash Point 322.2 °C
Density 1.38
Solubility DMSO: ≥20mg/mL
Appearance solid
Storage Desiccate at RT
Payment Western union, Bitcoin, XMR, USDT, TT
Delivery By sea, by air, all express modes (EMS,UPS,DHL,TNT,Fedex), 3-5 days after payment
Shipping adress Provide your valid and correct destination address info with post office code, phone number and consignee
Package Choose the most appropriate way according to quantity and safety degree
CAS 30123-17-2 Description

Tianeptine sodium salt is a salt of Tianeptine. Tianeptine is an atypical antidepressant. It is an agonist of the μ-opioid receptor (MOR; EC50s = 194 and 641 nM for human and mouse receptors, respectively, in a BRET assay for G protein activation) and also has effects on the glutamate system. Tianeptine (30 mg/kg) decreases immobility in the forced swim test in wild-type, but not MOR knockout mice, indicating antidepressant-like activity dependent on MORs. It increases locomotor activity at a dose of 30, but not 10 mg/kg, in the open field test and increases paw withdrawal latency in the hot-plate test in mice. Tianeptine modulates AMPA receptor activity by increasing phosphorylation of the AMPA receptor GluR1 subunit in the frontal cortex and hippocampal CA3 region in mice. It prevents increases in glial glutamate transporter 1 (GLT-1) expression induced by chronic restraint stress in the hippocampal CA3 region in rats when administered at a dose of 10 mg/kg per day for 21 days.5It also reverses increases in extracellular glutamate levels induced by acute restraint stress in the basolateral nucleus of the amygdala in rats.

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