N-Phenethyl-14-ethoxymetopon: Difference between revisions
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== N-Phenethyl-14-ethoxymetopon == | |||
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File:N-Phenethyl-14-ethoxymetopon.svg|N-Phenethyl-14-ethoxymetopon structure | |||
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Latest revision as of 22:16, 16 February 2025
N-Phenethyl-14-ethoxymetopon is a potent opioid analgesic drug that is structurally related to metopon and the morphinan family. It was developed by a team at the University of Alberta in the late 1990s.
Chemistry[edit]
N-Phenethyl-14-ethoxymetopon is a derivative of metopon, which itself is a derivative of hydromorphone. It is synthesized by replacing the N-methyl group of metopon with a phenethyl group, and the 14-hydroxy group with an ethoxy group. This modification results in a drug that is approximately 60 times more potent than morphine in its analgesic effects.
Pharmacology[edit]
Like other opioids, N-Phenethyl-14-ethoxymetopon acts on the mu opioid receptor to produce its analgesic effects. It is thought to be a full agonist at this receptor, meaning it can fully activate the receptor to produce its maximum possible response.
Clinical Use[edit]
Despite its potency, N-Phenethyl-14-ethoxymetopon is not currently used in clinical practice. Its development was primarily for research purposes, to better understand the structure-activity relationships of opioid drugs. However, its high potency and long duration of action suggest that it could potentially be useful in the treatment of severe chronic pain.
See Also[edit]
References[edit]
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N-Phenethyl-14-ethoxymetopon[edit]
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N-Phenethyl-14-ethoxymetopon structure
