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		<title>A-796,260 - Revision history</title>
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		<updated>2026-04-28T16:10:55Z</updated>
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	<entry>
		<id>http://www.wikiweed.com/index.php?title=A-796,260&amp;diff=1366&amp;oldid=prev</id>
		<title>Adm1n: Created page with &quot;'''A-796,260''' is a drug developed by Abbott Laboratories that acts as a potent and selective cannabinoid CB2 receptor agonist. Replacing the aromatic 3-benzoyl or 3-...&quot;</title>
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				<updated>2015-02-15T11:10:36Z</updated>
		
		<summary type="html">&lt;p&gt;Created page with &amp;quot;&amp;#039;&amp;#039;&amp;#039;A-796,260&amp;#039;&amp;#039;&amp;#039; is a drug developed by Abbott Laboratories that acts as a potent and selective &lt;a href=&quot;/Cannabinoid&quot; title=&quot;Cannabinoid&quot;&gt;cannabinoid&lt;/a&gt; &lt;a href=&quot;/CB2_receptor&quot; title=&quot;CB2 receptor&quot;&gt;CB2 receptor&lt;/a&gt; agonist. Replacing the aromatic 3-benzoyl or 3-...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;'''A-796,260''' is a drug developed by Abbott Laboratories that acts as a potent and selective [[cannabinoid]] [[CB2 receptor]] agonist. Replacing the aromatic 3-benzoyl or 3-naphthoyl group found in most indole derived cannabinoids with the 3-tetramethylcyclopropylmethanone group, imparts significant selectivity for CB2, and A-796,260 was found to be a highly selective CB2 agonist with little affinity for [[CB1]], having a CB2 Ki of 4.6 nM vs 945 nM at CB1.[1] It has potent analgesic and anti-inflammatory actions in animal models, being especially effective in models of neuropathic pain, but without producing [[cannabis]]-like behavioral effects.&lt;br /&gt;
&lt;br /&gt;
==See also==&lt;br /&gt;
&lt;br /&gt;
* [[A-834,735]]&lt;br /&gt;
* [[A-836,339]]&lt;br /&gt;
* [[JWH-200]]&lt;br /&gt;
* [[UR-144]]&lt;br /&gt;
* [[XLR-11 (drug)|XLR-11]]&lt;/div&gt;</summary>
		<author><name>Adm1n</name></author>	</entry>

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