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Cat. No. M2343
AM-2201 Structure
Size Price Availability Quantity
1mg USD 150 In stock
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Quality Control
Biological Activity

AM-2201 is a potent synthetic cannabinoid (CB) with Ki values of 1.0 and 2.6 nM for the CB1 and CB2 receptors, respectively. AM-2201 acts as a potent but nonselective full agonist for the cannabinoid receptor. The physiological actions and metabolism of AM2201 have not been characterized.

Customer Product Validations & Biological Datas
Source Drug Alcohol Depend (2017). Figure 2. AM2201
Method s.c.
Cell Lines Rats
Concentrations 0.1 – 0.3 mg/kg
Incubation Time 3 h
Results THC and XLR-11 were the least potent of the cannabinoids, while CP55,940 was the most potent. JWH-018 and AM2201 had comparable potency at increasing BP and were intermediate between CP55,940 and THC.
Conversion of different model animals based on BSA (Value based on data from FDA Draft Guidelines)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of resveratrol used for a mouse (22.4 mg/kg) to a dose based on the BSA for a rat, multiply 22.4 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for resveratrol of 11.2 mg/kg.

Chemical Information
Molecular Weight 359.44
Formula C24H22FNO
CAS Number 335161-24-5
Purity 100.00%
Storage at -20°C

Characteristics of the designer drug and synthetic cannabinoid receptor agonist AM-2201 regarding its chemistry and metabolism.
Hutter M, et al. J Mass Spectrom. 2013 Jul;48(7):885-94. PMID: 23832945.

First European case of convulsions related to analytically confirmed use of the synthetic cannabinoid receptor agonist AM-2201.
McQuade D, et al. Eur J Clin Pharmacol. 2013 Mar;69(3):373-6. PMID: 22936123.

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