46817-91-8

Viloxazine Chemical Structure
46817-91-8

Chemical Structure

Viloxazine

Synonym(s): Viloxazin; Emovit

  • CAS No.: 46817-91-8
  • Formula:C13H19NO3
  • Molecular Weight:237.29

IUPAC Name: 2-((2-ethoxyphenoxy)methyl)morpholine

InChIKey: YWPHCCPCQOJSGZ-UHFFFAOYSA-N

SMILES: CCOC1=C(C=CC=C1)OCC2OCCNC2

Biological Activity: Viloxazine is a non-brain-penetrant, selective norepinephrine transporter (NET) inhibitor (IC50= 0.26 μM) and 5-HT receptor modulator. Viloxazine antagonizes 5-HT2B receptors (Ki=4.2 μM) and agonizes 5-HT2C receptors (EC50= 32 μM), respectively, and enhances 5-HT neurotransmission by modulating 5-HT2B/C receptors. Viloxazine also competitively inhibits NET from increasing NE and DA levels in the synaptic cleft, and can be used in the study of attention deficit hyperactivity disorder (ADHD)[1][2][3].

Cat. No. Product Name Purity Description Pricing
HY-W380450
Viloxazine 99.15% Viloxazine is a non-brain-penetrant, selective norepinephrine transporter (NET) inhibitor (IC50= 0.26 μM) and 5-HT receptor modulator. Viloxazine antagonizes 5-HT2B receptors (Ki=4.2 μM) and agonizes 5-HT2C receptors (EC50= 32 μM), respectively, and enhances 5-HT neurotransmission by modulating 5-HT2B/C receptors. Viloxazine also competitively inhibits NET from increasing NE and DA levels in the synaptic cleft, and can be used in the study of attention deficit hyperactivity disorder (ADHD).
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HY-W380450R
Viloxazine (Standard) ≥98% Viloxazine is a non-brain-penetrant, selective norepinephrine transporter (NET) inhibitor (IC50= 0.26 μM) and 5-HT receptor modulator. Viloxazine antagonizes 5-HT2B receptors (Ki=4.2 μM) and agonizes 5-HT2C receptors (EC50= 32 μM), respectively, and enhances 5-HT neurotransmission by modulating 5-HT2B/C receptors. Viloxazine also competitively inhibits NET from increasing NE and DA levels in the synaptic cleft, and can be used in the study of attention deficit hyperactivity disorder (ADHD).
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USD 0.00

This product is a controlled substance and not for sale in your territory.

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