Viloxazine
CAS No. 46817-91-8
Viloxazine( —— )
Catalog No. M35400 CAS No. 46817-91-8
Viloxazine (Viloxazin) (Viloxazin) is a dual-action compound that functions as a norepinephrine reuptake inhibitor and exhibits potent agonistic activity towards 5-HT 2C receptors while acting as an antagonist for 5-HT 2B receptors.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 296 | Get Quote |
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| 5MG | 418 | Get Quote |
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| 10MG | 616 | Get Quote |
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| 25MG | 908 | Get Quote |
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| 50MG | 1279 | Get Quote |
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| 100MG | 1683 | Get Quote |
|
| 500MG | 3357 | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameViloxazine
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NoteResearch use only, not for human use.
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Brief DescriptionViloxazine (Viloxazin) (Viloxazin) is a dual-action compound that functions as a norepinephrine reuptake inhibitor and exhibits potent agonistic activity towards 5-HT 2C receptors while acting as an antagonist for 5-HT 2B receptors.
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DescriptionViloxazine (Viloxazin) is a norepinephrine reuptake inhibitor, also a potent 5-HT2C agonist and 5-HT2B antagonist with an EC50 of 32 μM and an IC50 of 27 μM for 5-HT2C and 5-HT2B, respectively. The mechanism of action of Viloxazine predominantly involves serotonergic and noradrenergic pathways. Viloxazine can be used for researching depression.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayGPCR/G Protein
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Target5-HT Receptor
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Recptor5-HT Receptor | Norepinephrine
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Research Area——
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Indication——
Chemical Information
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CAS Number46817-91-8
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Formula Weight237.29
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Molecular FormulaC13H19NO3
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Purity>98% (HPLC)
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Solubility——
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SMILESO(CC1CNCCO1)C2=C(OCC)C=CC=C2
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Yu C, et al. New Insights into the Mechanism of Action of Viloxazine: Serotonin and Norepinephrine Modulating Properties. J Exp Pharmacol. 2020 Aug 25;12:285-300.?
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Viloxazine
Viloxazine (Viloxazin) (Viloxazin) is a dual-action compound that functions as a norepinephrine reuptake inhibitor and exhibits potent agonistic activity towards 5-HT 2C receptors while acting as an antagonist for 5-HT 2B receptors.
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