| Weight | 237.299 g/mol |
|---|---|
| Formula | C13H19NO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 5 |
viloxazine (46817-91-8)
Vivalan · Viloxazine Hydrochloride · Emovit
Score:
#218 in Neurology
,
#993 in Neuroscience
,
#4350 in Biology
,
#5489 in Chemistry
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- Antidepressants and cognition: comparative effects of moclobemide, viloxazine and maprotiline (Psychopharmacology, 1992)
- Metabolism of some "second"- and "fourth"-generation antidepressants: iprindole, viloxazine, bupropion, mianserin, maprotiline, trazodone, nefazodone, and venlafaxine. (Cellular and Molecular Neurobiology, 1999)
- Effects of viloxazine, an antidepressant agent, on biogenic amine uptake mechanisms and related activities (Canadian Journal of Physiology and Pharmacology, 1976)
- Effects of viloxazine, its optical isomers and its major metabolites on biogenic amine uptake mechanisms in vitro and in vivo. (European Journal of Pharmacology, 1978)
- Viloxazine hydrochloride in narcolepsy: a preliminary report. (Sleep, 1986)
- Simultaneous Determination of Viloxazine, Venlafaxine, Imipramine, Desipramine, Sertraline, and Amoxapine in Whole Blood: Comparison of Two Extraction/Cleanup Procedures for Capillary Gas Chromatography with Nitrogen-Phosphorus Detection (Journal of Analytical Toxicology, 2002)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Vivalan
- Viloxazine Hydrochloride
- Emovit
- Viloxazine Oxalate (1:1)
- Astra Brand of Viloxazine Hydrochloride
- ICI58,834
- Viloxazine Hydrochloride, (S)-Isomer
- Viloxazine Hydrochloride, (R)-Isomer
- Viloxazine, (S)-Isomer
- ICI-58,834
- Viloxazine, (R)-Isomer
- Viloxazine, (+-)-Isomer
- AstraZeneca Brand of Viloxazine Hydrochloride
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SMILESCCOC1=CC=CC=C1OCC2CNCCO2
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InChIKeyYWPHCCPCQOJSGZ-UHFFFAOYSA-N
- Pubchem - viloxazine
- Wikipedia - viloxazine
Viloxazine (trade names Vivalan, Emovit, Vivarint and Vicilan) is a morpholine derivative and is a selective norepinephrine reuptake inhibitor (NRI). It was used as an antidepressant in some European countries, and produced a stimulant effect that is similar to the amphetamines, except without any signs of dependence. It was discovered and brought to market in 1976 by Imperial Chemical Industries and was withdrawn from the market in the early 2000s for business reasons.
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