Movatterモバイル変換

[0]ホーム
URL:

Jump to content
WikipediaThe Free Encyclopedia
Search

MMB-CHMICA

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
MMB-CHMICA
Clinical data
Other namesAMB-CHMICA
Legal status
Legal status
Identifiers
  • MethylN-{[1-(cyclohexylmethyl)-1H-indol-3-yl]carbonyl}-L-valinate
CAS Number
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC22H30N2O3
Molar mass370.493 g·mol−1
3D model (JSmol)
  • CC(C)[C@@H](C(=O)OC)NC(=O)c1cn(c2c1cccc2)CC3CCCCC3
  • InChI=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
  • Key:ROWZIXRLVUOMCJ-FQEVSTJZSA-N

MMB-CHMICA (AMB-CHMICA) is adesigner drug andsynthetic cannabinoid.[1][2][3] In 2018, it was the sixth-most common synthetic cannabinoid identified in drugs seized by theDrug Enforcement Administration.[4]

References

[edit]
  1. ^Göl E, Çok I (January 2019). "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.doi:10.1016/j.forsciint.2018.11.003.PMID 30502695.S2CID 56176934.
  2. ^Mardal M, Dalsgaard PW, Qi B, Mollerup CB, Annaert P, Linnet K (April 2018)."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.doi:10.1016/j.jchromb.2018.03.016.PMID 29549742.
  3. ^Wagmann L, Stiller RG, Fischmann S, Westphal F, Meyer MR (October 2022)."Going deeper into the toxicokinetics of synthetic cannabinoids: in vitro contribution of human carboxylesterases".Archives of Toxicology.96 (10):2755–2766.doi:10.1007/s00204-022-03332-z.PMC 9352624.PMID 35788413.S2CID 250281976.
  4. ^"Emerging Threat Report: Annual 2018"(PDF). Special Testing and Research Laboratory, Drug Enforcement Administration.
Phytocannabinoids
(comparison)
Cannabibutols
Cannabichromenes
Cannabicyclols
Cannabidiols
Cannabielsoins
Cannabigerols
Cannabiphorols
Cannabinols
Cannabitriols
Cannabivarins
Delta-3-tetrahydrocannabinols
Delta-4-tetrahydrocannabinols
Delta-7-tetrahydrocannabinols
Delta-8-tetrahydrocannabinols
Delta-9-tetrahydrocannabinols
Delta-10-Tetrahydrocannabinols
Delta-11-Tetrahydrocannabinols
Miscellaneous cannabinoids
Active metabolites
Endocannabinoids
Synthetic
cannabinoid
receptor
agonists /
neocannabinoids
Classical cannabinoids
(dibenzopyrans)
Non-classical
cannabinoids
Adamantoylindoles
Benzimidazoles
Benzoylindoles
Cyclohexylphenols
Eicosanoids
Indazole-3-
carboxamides
Indole-3-carboxamides
Indole-3-carboxylates
Naphthoylindazoles
Naphthoylindoles
Naphthoylpyrroles
Naphthylmethylindenes
Naphthylmethylindoles
Phenylacetylindoles
Pyrazolecarboxamides
Tetramethylcyclo-
propanoylindazoles
Tetramethylcyclo-
propanoylindoles
Others
AllostericCBRTooltip Cannabinoid receptorligands
Endocannabinoid
enhancers
(inactivation inhibitors)
Anticannabinoids
(antagonists/inverse
agonists/antibodies)
Retrieved from "https://en.wikipedia.org/w/index.php?title=MMB-CHMICA&oldid=1292486775"
Categories:
Hidden categories:
[8]ページ先頭
©2009-2025 Movatter.jp