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		<id>http://www.wikiweed.com/index.php?action=history&amp;feed=atom&amp;title=QUPIC</id>
		<title>QUPIC - Revision history</title>
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		<updated>2026-04-28T17:41:55Z</updated>
		<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>http://www.wikiweed.com/index.php?title=QUPIC&amp;diff=1375&amp;oldid=prev</id>
		<title>Adm1n: Created page with &quot;'''QUPIC (PB-22 or 1-pentyl-1H-indole-3-carboxylic acid 8-quinolinyl ester)''' is a designer drug offered by online vendors as a cannabimimetic agent, and detected being sold...&quot;</title>
		<link rel="alternate" type="text/html" href="http://www.wikiweed.com/index.php?title=QUPIC&amp;diff=1375&amp;oldid=prev"/>
				<updated>2015-02-15T11:36:08Z</updated>
		
		<summary type="html">&lt;p&gt;Created page with &amp;quot;&amp;#039;&amp;#039;&amp;#039;QUPIC (PB-22 or 1-pentyl-1H-indole-3-carboxylic acid 8-quinolinyl ester)&amp;#039;&amp;#039;&amp;#039; is a designer drug offered by online vendors as a cannabimimetic agent, and detected being sold...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;'''QUPIC (PB-22 or 1-pentyl-1H-indole-3-carboxylic acid 8-quinolinyl ester)''' is a designer drug offered by online vendors as a cannabimimetic agent, and detected being sold in [[Synthetic Cannabis]] products in Japan in 2013.The structure of QUPIC appears to use an understanding of structure-activity relationships within the indole class of cannabimimetics, although its design origins are unclear. QUPIC represents a structurally unique synthetic cannabinoid chemotype, since it contains an ester linker at the indole 3-position, rather than the precedented ketone of [[JWH-018]] and its analogs, or the amide of [[SDB-001]] and its analogs. No information regarding the in vitro activity of QUPIC has been published, however one in vivo study found [[PB-22]] to cause seizures in humans and dogs. QUPIC is an analog of JWH-018 which differs by having 8-hydroxyquinoline replacing the naphthalene group of JWH-018. QUPIC is now found in many herbal incense and potpourri products.&lt;br /&gt;
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== Detection ==&lt;br /&gt;
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A forensic standard of PB-22 is available, and the compound has been posted on the Forendex website of potential drugs of abuse.&lt;br /&gt;
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== Legal status ==&lt;br /&gt;
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As of 9 May 2014, PB-22 is no longer legal in New Zealand.&lt;br /&gt;
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In January 2014, QUPIC was designated as a Schedule I controlled substance in the United States.&lt;br /&gt;
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In Ohio, QUPIC is illegal.&lt;br /&gt;
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Florida also has banned QUPIC/P-22.&lt;br /&gt;
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Since 13.Dezember 2014 it is also illegal in Germany because of adding the substance to the BtMG Anlage II.&lt;br /&gt;
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==See also==&lt;br /&gt;
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* [[5F-PB-22]]&lt;br /&gt;
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* [[QUCHIC]]&lt;br /&gt;
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* [[SDB-001]]&lt;/div&gt;</summary>
		<author><name>Adm1n</name></author>	</entry>

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