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Desvenlafaxine succinate hydrate

Catalog No. T6188   CAS 386750-22-7
Synonyms: O-Desmethylvenlafaxine succinate hydrate, WY 45233 Succinate, Desvenlafaxine Succinate

Desvenlafaxine succinate hydrate (WY 45233 Succinate) is an antidepressant of the serotonin-norepinephrine reuptake inhibitor (SNRI).

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Desvenlafaxine succinate hydrate Chemical Structure
Desvenlafaxine succinate hydrate, CAS 386750-22-7
Pack Size Availability Price/USD Quantity
5 mg In stock $ 35.00
10 mg In stock $ 50.00
25 mg In stock $ 88.00
50 mg In stock $ 115.00
100 mg In stock $ 196.00
500 mg In stock $ 487.00
1 mL * 10 mM (in DMSO) In stock $ 45.00
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Purity: 99.39%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Desvenlafaxine succinate hydrate (WY 45233 Succinate) is an antidepressant of the serotonin-norepinephrine reuptake inhibitor (SNRI).
Targets&IC50 5-HT:40.2 nM(Ki), Norepinephrine:558.4 nM(Ki)
In vitro Desvenlafaxine succinate is the succinate salt monohydrate of O-desmethylvenlafaxine, an active metabolite of venlafaxine. Desvenlafaxine Succinate is a serotonin-norepinephrine reuptake inhibitor and is the active metabolite of the antidepressant venlafaxine. Similar to venlafaxine, Desvenlafaxine Succinate inhibits the neuronal uptake of serotonin and norepinephrine. Desvenlafaxine Succinate shows weak binding affinity (62% inhibition at 100 μM) at the human dopamine (DA) transporter. Desvenlafaxine Succinate inhibits [3H]5-HT or [3H]NE uptake for the hSERT or hNET with IC50 of 47.3 and 531.3 nM, respectively.[1] Desvenlafaxine Succinate has the potential to inhibit CYP2D6, which could result in increased concentrations of drugs metabolized through this pathway. Induction of CYP3A4 is also possible with Desvenlafaxine Succinate, which could impact the metabolism of drugs metabolized via this enzyme. [2]
In vivo Desvenlafaxine Succinate rapidly penetrates the male rat brain and hypothalamus. Desvenlafaxine Succinate significantly increases extracellular NE levels compared with baseline in the male rat hypothalamus but had no effect on DA levels using microdialysis. [1] Desvenlafaxine Succinate exhibits a linear and dose-proportional pharmacokinetic single-dose profile in a dose range from 100 to 600 mg/day. The absolute bioavailability of the oral formulation is 80.5%.[2]
Synonyms O-Desmethylvenlafaxine succinate hydrate, WY 45233 Succinate, Desvenlafaxine Succinate
Molecular Weight 399.48
Formula C20H33NO7
CAS No. 386750-22-7

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 50 mg/mL (125.16 mM)

TargetMolReferences and Literature

1. Deecher DC, et al. J Pharmacol Exp Ther, 2006, 318(2), 657-665. 2. Sopko MA Jr, et al. Ann Pharmacother, 2008, 42(10), 1439-1446.

Related compound libraries

This product is contained In the following compound libraries:
Inhibitor Library Drug Repurposing Compound Library GPCR Compound Library Anti-Cancer Drug Library Anti-Cancer Approved Drug Library Anti-Neurodegenerative Disease Compound Library Target-Focused Phenotypic Screening Library Anti-Cancer Compound Library CNS-Penetrant Compound Library Bioactive Compound Library

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Keywords

Desvenlafaxine succinate hydrate 386750-22-7 GPCR/G Protein Neuroscience 5-HT Receptor Serotonin Transporter Norepinephrine Desvenlafaxine succinate Hydrate O-Desmethylvenlafaxine succinate hydrate WY 45233 Succinate Inhibitor O-Desmethylvenlafaxine succinate Hydrate inhibit WY45233 Succinate O-Desmethylvenlafaxine succinate SERT Desvenlafaxine Succinate 5-HTT WY-45233 Succinate SLC6A4 inhibitor

 

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