MMB-CHMICA explained
| Iupac Name: | Methyl N--L-valinate |
| Width: | 150 |
| Legal Ca: | Schedule II |
| Legal De: | NpSG |
| Legal Uk: | PSA |
| Legal Us: | Schedule I |
| Cas Number: | 1971007-94-9 |
| Unii: | HEN6ZCR7GD |
| Chemspiderid: | 68896113 |
| Synonyms: | AMB-CHMICA |
| C: | 22 |
| H: | 30 |
| N: | 2 |
| O: | 3 |
| Smiles: | CC(C)[C@@H](C(=O)OC)NC(=O)c1cn(c2c1cccc2)CC3CCCCC3 |
| Stdinchi: | 1S/C22H30N2O3/c1-15(2)20(22(26)27-3)23-21(25)18-14-24(13-16-9-5-4-6-10-16)19-12-8-7-11-17(18)19/h7-8,11-12,14-16,20H,4-6,9-10,13H2,1-3H3,(H,23,25)/t20-/m0/s1 |
| Stdinchikey: | ROWZIXRLVUOMCJ-FQEVSTJZSA-N |
MMB-CHMICA (AMB-CHMICA) is a designer drug and synthetic cannabinoid.[1] [2] [3] In 2018, it was the sixth-most common synthetic cannabinoid identified in drugs seized by the Drug Enforcement Administration.[4]
Notes and References
- Göl E, Çok I . New psychoactive substances in Turkey: Narcotics cases assessed by the Council of Forensic Medicine between 2016 and 2017 in Ankara, Turkey . Forensic Science International . 294 . 113–123 . January 2019 . 30502695 . 10.1016/j.forsciint.2018.11.003 . 56176934 .
- Mardal M, Dalsgaard PW, Qi B, Mollerup CB, Annaert P, Linnet K . Metabolism of the synthetic cannabinoids AMB-CHMICA and 5C-AKB48 in pooled human hepatocytes and rat hepatocytes analyzed by UHPLC-(IMS)-HR-MSE . Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences . 1083 . 189–197 . April 2018 . 29549742 . 10.1016/j.jchromb.2018.03.016 .
- Wagmann L, Stiller RG, Fischmann S, Westphal F, Meyer MR . Going deeper into the toxicokinetics of synthetic cannabinoids: in vitro contribution of human carboxylesterases . Archives of Toxicology . 96 . 10 . 2755–2766 . October 2022 . 35788413 . 9352624 . 10.1007/s00204-022-03332-z . 250281976 .
- Web site: Emerging Threat Report: Annual 2018 . Special Testing and Research Laboratory, Drug Enforcement Administration .
