AB-CHMINACA
Chemical compound
From Wikipedia, the free encyclopedia
AB-CHMINACA is an indazole-based synthetic cannabinoid. It is a potent agonist of the CB1 receptor (Ki = 0.78 nM) and CB2 receptor (Ki = 0.45 nM) and fully substitutes for Δ9-THC in rat discrimination studies, while being 16x more potent.[3][4] Continuing the trend seen in other cannabinoids of this generation, such as AB-FUBINACA and AB-PINACA, it contains a valine amino acid amide residue as part of its structure, where older cannabinoids contained a naphthyl or adamantane residue.
- BR: Class F2 (Prohibited psychotropics)[1]
- CA: Schedule II
- DE: Anlage II (Authorized trade only, not prescriptible)
- UK: Class B
- US: Schedule I
- UN: Psychotropic Schedule II[2]
- Illegal in China and Switzerland
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| Formula | C20H28N4O2 |
| Molar mass | 356.470 g·mol−1 |
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Side effects
Legal status
In 2015, AB-CHMINACA became a Schedule I controlled substance in the United States.[12]
AB-CHMINACA is an Anlage II controlled substance in Germany as of May 2015.[13]
As of October 2015 AB-CHMINACA is a controlled substance in China.[14]
AB-CHMINACA is illegal in Switzerland as of December 2015.[15]
AB-CHMINACA is an illegal substance in Russian Federation.