Acetyldihydrocodeine: Difference between revisions

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[[Category:Analgesics]]
[[Category:Analgesics]]
[[Category:Semi-synthetic opioids]]
[[Category:Semi-synthetic opioids]]
<gallery>
File:Acetyldihydrocodeine.svg|Chemical structure of Acetyldihydrocodeine
File:Acetyldihydrocodeine_ball-and-stick.png|Ball-and-stick model of Acetyldihydrocodeine
</gallery>

Latest revision as of 02:07, 18 February 2025

A semi-synthetic opioid analgesic


Acetyldihydrocodeine
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Acetyldihydrocodeine is a semi-synthetic opioid analgesic that is derived from dihydrocodeine. It is used for the treatment of moderate to severe pain and is known for its effectiveness in pain management.

Pharmacology[edit]

Acetyldihydrocodeine is an opioid that acts primarily on the central nervous system to relieve pain. It binds to the opioid receptors, which are part of the G protein-coupled receptor family, and modulates the perception of pain. The drug is metabolized in the liver and excreted by the kidneys.

Medical uses[edit]

Acetyldihydrocodeine is prescribed for the relief of moderate to severe pain. It is often used in cases where other analgesics, such as nonsteroidal anti-inflammatory drugs (NSAIDs), are not effective. It may also be used in combination with other medications to enhance pain relief.

Side effects[edit]

Common side effects of acetyldihydrocodeine include nausea, vomiting, constipation, drowsiness, and dizziness. Like other opioids, it has the potential for addiction and abuse. Long-term use can lead to tolerance and physical dependence.

Legal status[edit]

The legal status of acetyldihydrocodeine varies by country. In some regions, it is classified as a controlled substance due to its potential for abuse and addiction. It is important for prescribers to adhere to local regulations when prescribing this medication.

Synthesis[edit]

Acetyldihydrocodeine is synthesized from dihydrocodeine through an acetylation process. This involves the introduction of an acetyl group to the dihydrocodeine molecule, enhancing its lipophilicity and potentially altering its pharmacokinetic properties.

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