Adm1n: /* See also */

2015-04-14T11:20:53Z

‎See also

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2015-04-14T11:13:43Z

‎See also

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2015-04-14T11:13:10Z

‎See also

Adm1n at 11:20, 15 February 2015

2015-02-15T11:20:45Z

Adm1n: Created page with "See at Cannabicyclohexanol"

2015-02-15T10:28:14Z

Created page with "See at Cannabicyclohexanol"

New page

See at [[Cannabicyclohexanol]]

@@ Line 52: / Line 52: @@
 * [[CP 55,244]]
 * [[CP 55,940]]
-* [[CP-945,598]]
+* [[Otenabant|CP-945,598]]
 * [[9-nor-9β-Hydroxyhexahydrocannabinol|HHC]]
 * [[O-1871]]

@@ Line 49: / Line 49: @@
 * [[Cannabicyclohexanol|(C8)-CP 47,497]]
 * [[(C9)-CP 47,497]]
-* [[CP 50,556-1]]
+* [[Levonantradol|CP 50,556-1]]
 * [[CP 55,244]]
 * [[CP 55,940]]

@@ Line 47: / Line 47: @@
 * [[(C6)-CP 47,497]]
-* [[(C8)-CP 47,497]]
+* [[Cannabicyclohexanol|(C8)-CP 47,497]]
 * [[(C9)-CP 47,497]]
 * [[CP 50,556-1]]

← Older revision		Revision as of 11:20, 15 February 2015
Line 1:		Line 1:
−	See at [[~~Cannabicyclohexanol~~]]	+	'''CP 47,497 or (C7)-CP 47,497''' is a [[cannabinoid]] receptor agonist drug, developed by Pfizer in the 1980s. It has analgesic effects and is used in scientific research. It is a potent [[CB1]] agonist with a Kd of 2.1nM.
		+
		+
		+	== Homologue ==
		+
		+	On the 19th of January 2009, the University of Freiburg in Germany announced that an analog of CP 47,497 is the main active ingredient in the herbal "incense" product Spice, specifically the 1,1-dimethyloctyl homologue of CP 47,497. Both the dimethylheptyl and dimethyloctyl homologues were detected in different batches, with considerable variation in the concentration present in different samples that were analysed. The weaker dimethylhexyl and dimethylnonyl homologues were not found in any batches of smoking blends tested, but have been legally scheduled alongside the others in some jurisdictions, to forestall any potential use for this purpose. The 1,1-dimethyloctyl homologue of CP 47,497 is in fact several times more potent than the parent compound, which is somewhat unexpected as the 1,1-dimethylheptyl is the most potent substituent in classical cannabinoid compounds such as [[HU-210]]. The unapproved use of these compounds in herbal smoking blends has led to a resurgence in legitimate scientific research into their use, and consequently the C8 homologue of CP 47,497 has been assigned a proper name, [[cannabicyclohexanol]].
		+
		+
		+	== Legal status ==
		+
		+	'''Germany'''
		+
		+	On 22 January 2009, CP 47,497 was added to the German controlled drug schedules ("Betäubungsmittelgesetz"), along with its dimethylhexyl, dimethyloctyl and dimethylnonyl homologues.
		+
		+
		+	'''France'''
		+
		+	CP 47,497 and its C6, C8, and C9 homologues were made illegal in France on 24 February 2009.
		+
		+
		+	'''Latvia'''
		+
		+	CP 47,497 and its C6, C8, and C9 homologues were made illegal in Latvia on 28 November 2009.
		+
		+
		+	'''Lithuania'''
		+
		+	CP 47,497 and its C6, C8, and C9 homologues were made illegal in Lithuania on 5 June 2009.
		+
		+
		+	'''Sweden'''
		+
		+	CP 47,497 and its C6, C7, C8, and C9 homologues were made illegal in Sweden on 15 September 2009.
		+
		+
		+	'''Romania'''
		+
		+	CP 47,497 and its C6, C7, C8, and C9 homologues were made illegal in Romania on 15 February 2010.(Illegal Substances in Romania after 15.02.2010
		+
		+
		+	'''United States'''
		+
		+	As of March 1, 2011, it is a schedule 1 drug.
		+
		+
		+	==See also==
		+
		+	* [[(C6)-CP 47,497]]
		+	* [[(C8)-CP 47,497]]
		+	* [[(C9)-CP 47,497]]
		+	* [[CP 50,556-1]]
		+	* [[CP 55,244]]
		+	* [[CP 55,940]]
		+	* [[CP-945,598]]
		+	* [[9-nor-9β-Hydroxyhexahydrocannabinol\|HHC]]
		+	* [[O-1871]]

CP 47,497 - Revision history

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Adm1n at 11:20, 15 February 2015

Adm1n: Created page with "See at Cannabicyclohexanol"