ArticleslgStudy

chemistry

Manifaxine

Manifaxine is a chemistry topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand Manifaxine rather than just read about it. In short: Manifaxine (developmental code name GW-320,659) is a norepinephrine–dopamine reuptake inhibitor developed by GlaxoSmithKline through structural modification of radafaxine, an isomer of hydroxybupropion and one of the active metabolites of bupropion. Manifaxine was researched for treatment of attention deficit hyperactivity disorder (ADHD) and obesity and was found to be safe, reasonably effective, and well-tolerated…

Manifaxine — main illustration
Manifaxine — illustration

Key takeaways

  • Manifaxine belongs to chemistry; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect Manifaxine to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of Manifaxine from memory before moving on to harder problems.

Reference excerpt

Manifaxine (developmental code name GW-320,659) is a norepinephrine–dopamine reuptake inhibitor developed by GlaxoSmithKline through structural modification of radafaxine, an isomer of hydroxybupropion and one of the active metabolites of bupropion. Manifaxine was researched for treatment of attention deficit hyperactivity disorder (ADHD) and obesity and was found to be safe, reasonably effective, and well-tolerated for both applications. However, no results were reported following these initial trials and development was discontinued.

Synthesis

The Grignard reaction between 3,5-difluorobenzonitrile (1) and ethylmagnesium bromide gives 3,5-difluoropropiophenone (2). Halogenation with molecular bromine occurs at the alpha-keto position providing 2-bromo-3',5'-difluoropropiophenone (3). Intermolecular ring formation with DL-alaninol (2-aminopropanol) completes the synthesis of manifaxine (4).

See also 3,5-Difluoromethcathinone 3-Fluorophenmetrazine

References

Illustrations

Manifaxine illustration
Manifaxine: Synthesis:[4] Patent:[5] See also:[6][7]
Synthesis:[4] Patent:[5] See also:[6][7]

Worked examples

Example 1 — a first encounter with Manifaxine

Start with the simplest possible case. Write down what Manifaxine claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In chemistry, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to Manifaxine before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about Manifaxine ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of Manifaxine

In research
Manifaxine appears in chemistry research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses Manifaxine in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
Manifaxine is common in secondary-school and first-year university syllabi. It links to neighbouring topics 3,5-Difluorophenyl compounds, Abandoned drugs, Beta-Hydroxyamphetamines, so understanding it makes those chapters shorter.
In everyday life
Look for Manifaxine outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.
Ask Teacher Smith questions about this articleOpens your AI tutor with a question about “Manifaxine” →

Affiliate

Preply — study more efficiently by working with a personal tutor. 50% off.

How to study Manifaxine in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Manifaxine means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain Manifaxine out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Manifaxine in simple terms?

Manifaxine (developmental code name GW-320,659) is a norepinephrine–dopamine reuptake inhibitor developed by GlaxoSmithKline through structural modification of radafaxine, an isomer of hydroxybupropion and one of the active metabolites of bupropion. Manifaxine was researched for treatment of attent…

Why does Manifaxine matter?

Because it connects several chemistry ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study Manifaxine?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on Manifaxine.

Tags

  • 3,5-Difluorophenyl compounds
  • Abandoned drugs
  • Beta-Hydroxyamphetamines
  • Drugs developed by GSK plc
  • Drugs not assigned an ATC code
  • Norepinephrine–dopamine reuptake inhibitors
  • Phenylmorpholines
  • Stimulants
  • Tertiary alcohols

Keep exploring