Bioactivity | 6-Iodopravadoline (AM630) TFA is a selective cannabinoid CB2 receptor antagonist (Ki=31.2 nM) that displays 165-fold selectivity over CB1 receptors. 6-Iodopravadoline TFA attenuates the ability of a number of cannabinoids to inhibit electrically-evoked twitches of the mouse isolated vas deferens[1][2]. |
In Vivo | 6-Iodopravadoline (AM630) (2, 3 mg/kg, i.p.; Swiss ICR mice) TFA significantly reduces the time spent in the light box compared with vehicle group. 6-Iodopravadoline (AM630) (1, 2 or 3 mg/kg, i.p., twice a day; Swiss ICR mice) TFA produces a significant anxiolytic effect, increasing the time spent in the light box at all of the doses used[3]. |
Name | 6-Iodopravadoline TFA |
Formula | C25H26F3IN2O5 |
Molar Mass | 618.38 |
Transport | Room temperature in continental US; may vary elsewhere. |
Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Reference | [1]. García-Gutiérrez MS, et al. Chronic blockade of cannabinoid CB2 receptors induces anxiolytic-like actions associated with alterations in GABA(A) receptors. Br J Pharmacol. 2012;165(4):951-964. [2]. Pertwee R, et al. AM630, a competitive cannabinoid receptor antagonist. Life Sci. 1995;56(23-24):1949-1955. |