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	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Acetylfentanyl</id>
	<title>Acetylfentanyl - Revision history</title>
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	<updated>2026-04-26T16:29:30Z</updated>
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		<id>https://wikimd.org/index.php?title=Acetylfentanyl&amp;diff=5831449&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
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		<updated>2024-05-27T01:22:51Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;[[File:Acetylfentanyl.svg|thumb|Acetylfentanyl|right]] [[File:Acetylfentanyl 3D BS.png|thumb|Acetylfentanyl 3D BS.png]] {{Short description|Synthetic opioid analgesic}}&lt;br /&gt;
{{Drugbox&lt;br /&gt;
| verifiedrevid = 477318705&lt;br /&gt;
| image = Acetylfentanyl.svg&lt;br /&gt;
| width = 200&lt;br /&gt;
| image2 = &lt;br /&gt;
| width2 = &lt;br /&gt;
| tradename = &lt;br /&gt;
| synonyms = &lt;br /&gt;
| IUPAC_name = N-Phenyl-N-[1-(2-phenylethyl)piperidin-4-yl]acetamide&lt;br /&gt;
| CAS_number = 3258-84-2&lt;br /&gt;
| ATC_prefix = &lt;br /&gt;
| ATC_suffix = &lt;br /&gt;
| PubChem = 62157&lt;br /&gt;
| DrugBank = &lt;br /&gt;
| ChemSpiderID = 55980&lt;br /&gt;
| UNII = &lt;br /&gt;
| KEGG = &lt;br /&gt;
| ChEBI = &lt;br /&gt;
| ChEMBL = &lt;br /&gt;
| IUPHAR_ligand = &lt;br /&gt;
| C=21 | H=26 | N=2 | O=1&lt;br /&gt;
| smiles = CC(=O)N(C1CCN(CC1)CC2=CC=CC=C2)C3=CC=CC=C3&lt;br /&gt;
| StdInChI = 1S/C21H26N2O/c1-18(24)23(20-10-6-2-7-11-20)21-13-16-22(17-14-21)15-19-8-4-3-5-9-19/h2-11,21H,12-17H2,1H3&lt;br /&gt;
| StdInChIKey = YXKTVDFXDRQTKV-UHFFFAOYSA-N&lt;br /&gt;
| StdInChI_Ref = &lt;br /&gt;
| StdInChIKey_Ref = &lt;br /&gt;
}}&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Acetylfentanyl&amp;#039;&amp;#039;&amp;#039; is a [[synthetic opioid]] analgesic that is an analog of [[fentanyl]]. It is a potent [[agonist]] of the [[mu-opioid receptor]] and has been associated with numerous [[overdose]] deaths.&lt;br /&gt;
==Chemical structure and properties==&lt;br /&gt;
Acetylfentanyl is chemically similar to [[fentanyl]], with the primary difference being the presence of an acetyl group in place of the [[propionyl group]] found in fentanyl. Its [[IUPAC name]] is N-Phenyl-N-[1-(2-phenylethyl)piperidin-4-yl]acetamide. The molecular formula is C21H26N2O.&lt;br /&gt;
==Pharmacology==&lt;br /&gt;
Acetylfentanyl acts as a potent [[agonist]] at the [[mu-opioid receptor]], which is responsible for its analgesic and euphoric effects. It is estimated to be 5 to 15 times more potent than [[heroin]] and about 80 times more potent than [[morphine]]. The drug&amp;#039;s high potency increases the risk of [[overdose]] and [[respiratory depression]].&lt;br /&gt;
==Medical use==&lt;br /&gt;
Acetylfentanyl has no approved medical use and is not prescribed for any condition. It is often encountered as a [[designer drug]] and is sometimes found in [[illicit drug]] supplies, either alone or mixed with other substances.&lt;br /&gt;
==Legal status==&lt;br /&gt;
The legal status of acetylfentanyl varies by country. In many jurisdictions, it is classified as a controlled substance due to its high potential for abuse and lack of accepted medical use. For example, in the [[United States]], it is classified as a [[Schedule I]] substance under the [[Controlled Substances Act]].&lt;br /&gt;
==Health risks==&lt;br /&gt;
The primary health risks associated with acetylfentanyl are related to its potency and potential for overdose. Symptoms of overdose may include severe [[respiratory depression]], [[sedation]], [[coma]], and death. [[Naloxone]] can be used to reverse the effects of an acetylfentanyl overdose, but multiple doses may be required due to the drug&amp;#039;s potency.&lt;br /&gt;
==See also==&lt;br /&gt;
* [[Fentanyl]]&lt;br /&gt;
* [[Opioid]]&lt;br /&gt;
* [[Designer drug]]&lt;br /&gt;
* [[Overdose]]&lt;br /&gt;
==References==&lt;br /&gt;
{{Reflist}}&lt;br /&gt;
[[Category:Opioids]]&lt;br /&gt;
[[Category:Synthetic opioids]]&lt;br /&gt;
[[Category:Designer drugs]]&lt;br /&gt;
[[Category:Analgesics]]&lt;br /&gt;
[[Category:Schedule I controlled substances]]&lt;br /&gt;
[[Category:Mu-opioid receptor agonists]]&lt;br /&gt;
{{medicine-stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
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