56287-61-7
Chemical Structure
(S)-Viloxazine hydrochloride
Synonym(s): (S)-Viloxazin hydrochloride; (S)-Emovit hydrochloride
- CAS No.: 56287-61-7
- Formula:C13H20ClNO3
- Molecular Weight:273.76
IUPAC Name: (S)-2-((2-ethoxyphenoxy)methyl)morpholine hydrochloride
InChIKey: HJOCKFVCMLCPTP-MERQFXBCSA-N
SMILES: CCOC1=CC=CC=C1OC[C@@H]2CNCCO2.Cl
Biological Activity: (S)-Viloxazine hydrochloride is the isomer of Viloxazine hydrochloride (HY-125784). Viloxazine hydrochloride is the hydrochloride salt form of Viloxazine (HY-W380450). Viloxazine (Viloxazin) hydrochloride is a norepinephrine reuptake inhibitor and a potent 5-HT2C agonist agent and 5-HT2B antagonist，EC50 for 5-HT2C b> is 32 μM，and the IC50 for 5-HT2B is 27 μM. Viloxazine hydrochloride's mechanism of action primarily involves serotonergic and noradrenergic pathways. Viloxazine hydrochloride is used in antidepressant research[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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(S)-Viloxazine hydrochloride | 99.90% | (S)-Viloxazine hydrochloride is the isomer of Viloxazine hydrochloride (HY-125784). Viloxazine hydrochloride is the hydrochloride salt form of Viloxazine (HY-W380450). Viloxazine (Viloxazin) hydrochloride is a norepinephrine reuptake inhibitor and a potent 5-HT2C agonist agent and 5-HT2B antagonist，EC50 for 5-HT2C b> is 32 μM，and the IC50 for 5-HT2B is 27 μM. Viloxazine hydrochloride's mechanism of action primarily involves serotonergic and noradrenergic pathways. Viloxazine hydrochloride is used in antidepressant research. | ||||||||||||||||||||
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(S)-Viloxazine-d5 hydrochloride | 98.19% | (S)-Viloxazine-d5 (hydrochloride) is the deuterium labeled (S)-Viloxazine hydrochloride. | ||||||||||||||||||||
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References
- [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. [Content Brief]
- [2]. Pinder RM, et al. Viloxazine: a review of its pharmacological properties and therapeutic efficacy in depressive illness. Drugs. 1977 Jun;13(6):401-21. [Content Brief]
