AM-2232
CAS No. 335161-19-8
AM-2232 ( AM 2232; AM2232; UNII-40KCH8YIKP )
Catalog No. M27408 CAS No. 335161-19-8
AM-2232 is a potent and unselective agonist of the cannabinoid receptors.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
2MG | 128 | Get Quote |
|
5MG | 177 | Get Quote |
|
10MG | 304 | Get Quote |
|
25MG | 516 | Get Quote |
|
50MG | 737 | Get Quote |
|
100MG | 1017 | Get Quote |
|
500MG | 2052 | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameAM-2232
-
NoteResearch use only, not for human use.
-
Brief DescriptionAM-2232 is a potent and unselective agonist of the cannabinoid receptors.
-
DescriptionAM-2232 is a potent and unselective agonist of the cannabinoid receptors.
-
SynonymsAM 2232; AM2232; UNII-40KCH8YIKP
-
PathwayGPCR/G Protein
-
TargetCannabinoid Receptor
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number335161-19-8
-
Formula Weight352.4
-
Molecular FormulaC24H20N2O
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C(c1cn(CCCCC#N)c2ccccc12)c1cccc2ccccc12
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Mahmood BrobbeyOppong, et al. Secondary metabolites from Sterculia lychnophora Hance (Pangdahai). Biochemical Systematics and Ecology, Volume 92, October 2020, 104125.
molnova catalog
related products
-
APD-371
APD-371 (APD371, Olorinab)is a potent, selective and orally available CB2 agonist with EC50 of 6.2 nM; displays no activity against CB1 receptors (EC50>10 uM).
-
Otenabant
A potent, and selective CB1 receptor antagonist with Ki of 0.7 nM/0.12 nM in binding and functional assays respectively; has low affinity (Ki=7600 nM) for human CB2 receptors; reverses cannabinoid agonist mediated responses, reduces food intake, and increases energy expenditure and fat oxidation in rodents.ObesityPhase 3 Discontinued
-
AM-630
A potent and selective inverse agonist for the cannabinoid receptor CB2 with Ki of 32.1 nM, 165-fold selectivity over CB1.