Difference between revisions of "ADB-FUBINACA"

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(Created page with "'''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...")
 
 
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'''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.
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'''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 (drug)|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.
  
 
==See also==
 
==See also==

Latest revision as of 04:33, 14 April 2015

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 andSTS-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.

See also