35604-67-2

Viloxazine hydrochloride Chemical Structure
35604-67-2

Chemical Structure

Viloxazine hydrochloride

Synonym(s): Viloxazin hydrochloride; Emovit hydrochloride

  • CAS. Nr.: 35604-67-2
  • Formula:C13H20ClNO3
  • Molecular Weight:273.76

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

InChIKey: HJOCKFVCMLCPTP-UHFFFAOYSA-N

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

Biological Activity: Viloxazine hydrochloride 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].

Art. -Nr. Produktname Reinheit Beschreibung Pricing
HY-125784
Viloxazine hydrochloride 98.94% Viloxazine hydrochloride 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-125784S
(rac)-Viloxazine-d5 hydrochloride (rac)-Viloxazine-d5 (hydrochloride) is the deuterium labeled (rac)-Viloxazine hydrochloride.
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