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ADB-FUBINACA
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ADB-FUBINACA : ウィキペディア英語版
ADB-FUBINACA

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 and has been reported to be a a potent agonist of the CB1 receptor and CB2 receptor with a EC50 value of 1.2 nM and 3.5 nM respectively.〔(Buchler IP et al, INDAZOLE DERIVATIVES. WO 2009/106982 )〕 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.
An analogue of ADB-FUBINACA, ADSB-FUB-187, containing a more functionalized carboxamide substituent was recently reported.
==See also==

* 5F-AB-PINACA
* 5F-ADB
* 5F-AMB
* 5F-APINACA
* AB-CHFUPYCA
* AB-FUBINACA
* AB-PINACA
* ADB-CHMINACA
* ADB-PINACA
* ADBICA
* ADSB-FUB-187
* APINACA
* MDMB-CHMICA
* MDMB-FUBINACA
* PF-03550096
* PX-3

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「ADB-FUBINACA」の詳細全文を読む



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