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		<id>http://www.wikiweed.com/index.php?action=history&amp;feed=atom&amp;title=ADB-FUBINACA</id>
		<title>ADB-FUBINACA - Revision history</title>
		<link rel="self" type="application/atom+xml" href="http://www.wikiweed.com/index.php?action=history&amp;feed=atom&amp;title=ADB-FUBINACA"/>
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		<updated>2026-04-28T19:40:34Z</updated>
		<subtitle>Revision history for this page on the wiki</subtitle>
		<generator>MediaWiki 1.24.1</generator>

	<entry>
		<id>http://www.wikiweed.com/index.php?title=ADB-FUBINACA&amp;diff=3243&amp;oldid=prev</id>
		<title>Adm1n at 11:33, 14 April 2015</title>
		<link rel="alternate" type="text/html" href="http://www.wikiweed.com/index.php?title=ADB-FUBINACA&amp;diff=3243&amp;oldid=prev"/>
				<updated>2015-04-14T11:33:51Z</updated>
		
		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
				&lt;col class='diff-marker' /&gt;
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				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;Revision as of 11:33, 14 April 2015&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 1:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 1:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;'''ADB-FUBINACA''' is a designer drug identified in [[synthetic cannabis]] blends in Japan in 2013. The (S) enantiomer of ADB-FUBINACA is claimed in Pfizer patent WO 2009/106982, with a Ki value of 0.36nM at CB1. ADB-FUBINACA features a carboxamide group at the 3-indazole position, like [[SDB-001]] and[[ STS-135]]. ADB-FUBINACA appears to be the product of rational drug design, since it differs from [[AB-FUBINACA]] only by the replacement of the isopropyl group with a tert-butyl group. The stereochemistry of the tert-butyl side-chain in the illicitly sold product is unresolved. Nothing is known of the pharmacological activity of ADB-FUBINACA in humans or other animals.&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;'''ADB-FUBINACA''' is a designer drug identified in [[synthetic cannabis]] blends in Japan in 2013. The (S) enantiomer of ADB-FUBINACA is claimed in Pfizer patent WO 2009/106982, with a Ki value of 0.36nM at CB1. ADB-FUBINACA features a carboxamide group at the 3-indazole position, like [[SDB-001]] and[[&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;STS-135 (drug)|&lt;/ins&gt;STS-135]]. ADB-FUBINACA appears to be the product of rational drug design, since it differs from [[AB-FUBINACA]] only by the replacement of the isopropyl group with a tert-butyl group. The stereochemistry of the tert-butyl side-chain in the illicitly sold product is unresolved. Nothing is known of the pharmacological activity of ADB-FUBINACA in humans or other animals.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;==See also==&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background-color: #f9f9f9; color: #333333; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #e6e6e6; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;==See also==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Adm1n</name></author>	</entry>

	<entry>
		<id>http://www.wikiweed.com/index.php?title=ADB-FUBINACA&amp;diff=1322&amp;oldid=prev</id>
		<title>Adm1n: Created page with &quot;'''ADB-FUBINACA''' is a designer drug identified in synthetic cannabis blends in Japan in 2013. The (S) enantiomer of ADB-FUBINACA is claimed in Pfizer patent WO 2009/1069...&quot;</title>
		<link rel="alternate" type="text/html" href="http://www.wikiweed.com/index.php?title=ADB-FUBINACA&amp;diff=1322&amp;oldid=prev"/>
				<updated>2015-02-15T02:27:05Z</updated>
		
		<summary type="html">&lt;p&gt;Created page with &amp;quot;&amp;#039;&amp;#039;&amp;#039;ADB-FUBINACA&amp;#039;&amp;#039;&amp;#039; is a designer drug identified in &lt;a href=&quot;/Synthetic_cannabis&quot; title=&quot;Synthetic cannabis&quot;&gt;synthetic cannabis&lt;/a&gt; blends in Japan in 2013. The (S) enantiomer of ADB-FUBINACA is claimed in Pfizer patent WO 2009/1069...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;'''ADB-FUBINACA''' is a designer drug identified in [[synthetic cannabis]] blends in Japan in 2013. The (S) enantiomer of ADB-FUBINACA is claimed in Pfizer patent WO 2009/106982, with a Ki value of 0.36nM at CB1. ADB-FUBINACA features a carboxamide group at the 3-indazole position, like [[SDB-001]] and[[ STS-135]]. ADB-FUBINACA appears to be the product of rational drug design, since it differs from [[AB-FUBINACA]] only by the replacement of the isopropyl group with a tert-butyl group. The stereochemistry of the tert-butyl side-chain in the illicitly sold product is unresolved. Nothing is known of the pharmacological activity of ADB-FUBINACA in humans or other animals.&lt;br /&gt;
&lt;br /&gt;
==See also==&lt;br /&gt;
* [[AB-FUBINACA]]&lt;br /&gt;
* [[ADB-PINACA]]&lt;br /&gt;
* [[ADBICA]]&lt;br /&gt;
* [[APINACA]]&lt;br /&gt;
* [[PF-03550096]]&lt;br /&gt;
* [[SDB-001]]&lt;br /&gt;
* [[STS-135 (drug)|STS-135]]&lt;/div&gt;</summary>
		<author><name>Adm1n</name></author>	</entry>

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