R-1 methanandamide is the most potent CB1 receptor agonist in the methanandamide series. It has a Ki value of 20 nM for the CB1 receptor, which is four-fold lower than that of arachidonoyl ethanolamide (AEA) (Ki =78 nM). In addition, R-1 methanandamide is more resistant than AEA to hydrolytic inactivation by fatty acid amide hydrolase. The Ki value for binding to the CB2 receptor from mouse spleen is 815 nM.
产品描述
The most potent CB1 receptor agonist in the methanandamide series with a Ki value of 20 nM for the CB1 receptor, which is four-fold lower than that of AEA (Ki =78 nM); more resistant than AEA to hydrolytic inactivation by FAAH; binds to the CB2 receptor from murine spleen with a Ki value of 815 nM