Difference between revisions of "QUCHIC"
(Created page with "'''QUCHIC (BB-22 or 1-(cyclohexylmethyl)-1H-indole-3-carboxylic acid 8-quinolinyl ester)''' is a designer drug offered by online vendors as a cannabimimetic agent, and was fir...") |
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| − | '''QUCHIC (BB-22 or 1-(cyclohexylmethyl)-1H-indole-3-carboxylic acid 8-quinolinyl ester)''' is a designer drug offered by online vendors as a cannabimimetic agent, and was first detected being sold in [[Synthetic | + | '''QUCHIC (BB-22 or 1-(cyclohexylmethyl)-1H-indole-3-carboxylic acid 8-quinolinyl ester)''' is a designer drug offered by online vendors as a cannabimimetic agent, and was first detected being sold in [[Synthetic Cannabis]] products in Japan in early 2013, and subsequently also in New Zealand. The structure of QUCHIC appears to utilise an understanding of structure-activity relationships within the indole class of cannabimimetics, although its design origins are unclear. QUCHIC, along with [[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 analogues, or the amide of [[SDB-001]] and its analogues. No information regarding the in vitro or in vivo activity of QUCHIC has been published, and only anecdotal reports are known of its pharmacology in humans or other animals. |
==See also== | ==See also== | ||
Latest revision as of 03:31, 15 February 2015
QUCHIC (BB-22 or 1-(cyclohexylmethyl)-1H-indole-3-carboxylic acid 8-quinolinyl ester) is a designer drug offered by online vendors as a cannabimimetic agent, and was first detected being sold in Synthetic Cannabis products in Japan in early 2013, and subsequently also in New Zealand. The structure of QUCHIC appears to utilise an understanding of structure-activity relationships within the indole class of cannabimimetics, although its design origins are unclear. QUCHIC, along with 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 analogues, or the amide of SDB-001 and its analogues. No information regarding the in vitro or in vivo activity of QUCHIC has been published, and only anecdotal reports are known of its pharmacology in humans or other animals.
