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		<title>HU-210 - Revision history</title>
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		<updated>2026-05-01T14:23:01Z</updated>
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		<id>http://www.wikiweed.com/index.php?title=HU-210&amp;diff=1260&amp;oldid=prev</id>
		<title>Adm1n: Created page with &quot;HU-210 is a synthetic cannabinoid that was first synthesized in 1988 from (1R,5S)-myrtenol by a group led by Professor Raphael Mechoulam at the Hebrew University. HU-210 is 10...&quot;</title>
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				<updated>2015-02-14T13:29:24Z</updated>
		
		<summary type="html">&lt;p&gt;Created page with &amp;quot;HU-210 is a synthetic cannabinoid that was first synthesized in 1988 from (1R,5S)-myrtenol by a group led by Professor Raphael Mechoulam at the Hebrew University. HU-210 is 10...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;HU-210 is a synthetic cannabinoid that was first synthesized in 1988 from (1R,5S)-myrtenol by a group led by Professor Raphael Mechoulam at the Hebrew University. HU-210 is 100 to 800 times more potent than natural THC from cannabis and has an extended duration of action. HU-210 is the (–)-1,1-dimethylheptyl analog of 11-hydroxy- Δ8- [[tetrahydrocannabinol]]; in some references it is called 1,1-dimethylheptyl- 11-hydroxytetrahydrocannabinol. The abbreviation &amp;quot;HU&amp;quot; stands for Hebrew University.&lt;br /&gt;
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The (+) enantiomer of HU-210 has almost all of the cannabinoid activity, with the (−) enantiomer HU-211 being inactive as a cannabinoid but instead acting as an NMDA antagonist having neuroprotective effects.&lt;br /&gt;
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HU-210 promotes proliferation, but not differentiation, of cultured embryonic hippocampal neural stem and progenitor cells likely via a sequential activation of [[CB1]] receptors, Gi/o proteins, and ERK signaling. It was also indicated by this increased neural growth to entail antianxiety and antidepressant effects.&lt;br /&gt;
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HU-210, alongside other synthetic cannabinoids like WIN 55,212-2 and JWH-133, is implicated in preventing the inflammation caused by amyloid beta proteins involved in Alzheimer's disease, in addition to preventing cognitive impairment and loss of neuronal markers. This anti-inflammatory action is induced through the activation of [[cannabinoid receptors]], which prevents microglial activation that elicits the inflammation. In addition, cannabinoids completely abolish neurotoxicity related to microglia activation in rat models.&lt;br /&gt;
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HU-210 is a potent analgesic with many of the same effects as natural [[THC]].&lt;br /&gt;
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== Recreational use ==&lt;br /&gt;
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According to the U.S. Customs and Border Protection, HU-210 was discovered in Spice Gold incense products seized at the US border in January 2009. Over 100 pounds of Spice products were seized based on this finding. HU-210 was also detected in three Spice products in the UK, as reported in June 2009.&lt;br /&gt;
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== Legal status ==&lt;br /&gt;
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'''United States'''&lt;br /&gt;
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HU-210 is a schedule I controlled substance under the Controlled Substances Act. &lt;br /&gt;
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To view national schedule, see: List of Schedule I drugs (US), &lt;br /&gt;
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'''New Zealand'''&lt;br /&gt;
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Banned in New Zealand as of 8 May 2014. &lt;br /&gt;
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== Other HU Cannabinoids ==&lt;br /&gt;
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*[[HU-211]]&lt;br /&gt;
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*[[HU-239]]&lt;br /&gt;
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*[[HU-243]]&lt;br /&gt;
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*[[HU-308]]&lt;br /&gt;
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*[[HU-320]]&lt;br /&gt;
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*[[HU-331]]&lt;br /&gt;
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*[[HU-336]]&lt;br /&gt;
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*[[HU-345]]&lt;br /&gt;
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== See also ==&lt;br /&gt;
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*[[CP 47,497]]&lt;br /&gt;
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*[[JWH-018]]&lt;/div&gt;</summary>
		<author><name>Adm1n</name></author>	</entry>

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