Viloxazine

From WikiMD.org
Jump to navigation Jump to search

Viloxazine

Viloxazine (pronounced: vi-lox-a-zine) is a Selective Norepinephrine Reuptake Inhibitor (NRI) that was previously used as an antidepressant. Viloxazine was discovered and developed in the 1970s by Imperial Chemical Industries (ICI), which merged into AstraZeneca in 1993.

Etymology

The term "Viloxazine" is derived from the systematic (IUPAC) name: 2-[(2-Ethoxyphenoxy)methyl]morpholine. The name is a combination of parts of its chemical structure, which includes a morpholine ring and an ethoxyphenyl group.

Usage

Viloxazine was used in some European countries for the treatment of depression until it was discontinued due to unprofitability. It is currently being investigated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) and Narcolepsy by Supernus Pharmaceuticals.

Mechanism of Action

Viloxazine inhibits the reuptake of norepinephrine, thereby increasing the amount of norepinephrine in the brain. This is thought to help alleviate symptoms of depression and ADHD.

Related Terms

External links

Esculaap.svg

This WikiMD article is a stub. You can help make it a full article.


Languages: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski