Biologically Active Small Molecules

An internal standard for the quantification of arachidonic acid by GC- or LC-MS.

An internal standard for the quantification of arachidonic acid by GC- or LC-MS.

A potent, stable, and selective agonist analog of AEA with a Ki value of 1.4 nM at the isolated rat CB1 receptor 1,400 times more potent at the CB1 compared with the CB2 receptor induces hypothermia in mice with the same efficacy as AEA, in spite

A potent, stable, and selective agonist analog of AEA with a Ki value of 1.4 nM at the isolated rat CB1 receptor 1,400 times more potent at the CB1 compared with the CB2 receptor induces hypothermia in mice with the same efficacy as AEA, in spite

A potent, stable, and selective agonist analog of AEA with a Ki value of 1.4 nM at the isolated rat CB1 receptor 1,400 times more potent at the CB1 compared with the CB2 receptor induces hypothermia in mice with the same efficacy as AEA, in spite

A potent, stable, and selective agonist analog of AEA with a Ki value of 1.4 nM at the isolated rat CB1 receptor 1,400 times more potent at the CB1 compared with the CB2 receptor induces hypothermia in mice with the same efficacy as AEA, in spite

Arachidonamide is an analog of AEA that lacks the hydroxyethyl moiety. It is hydrolyzed by FAAH more effectively than AEA but exhibits significantly weaker binding to the human CB1 receptor with a Ki value of 9.

Arachidonamide is an analog of AEA that lacks the hydroxyethyl moiety. It is hydrolyzed by FAAH more effectively than AEA but exhibits significantly weaker binding to the human CB1 receptor with a Ki value of 9.

Arachidonamide is an analog of AEA that lacks the hydroxyethyl moiety. It is hydrolyzed by FAAH more effectively than AEA but exhibits significantly weaker binding to the human CB1 receptor with a Ki value of 9.

Arachidonamide is an analog of AEA that lacks the hydroxyethyl moiety. It is hydrolyzed by FAAH more effectively than AEA but exhibits significantly weaker binding to the human CB1 receptor with a Ki value of 9.

A potent, stable, and selective agonist analog of AEA with a Ki value of 2.2 nM at the isolated rat CB1 receptor 325 times more potent at the CB1 receptor compared with the CB2 receptor induces hypothermia in mice with the same efficacy as AEA, in

A potent, stable, and selective agonist analog of AEA with a Ki value of 2.2 nM at the isolated rat CB1 receptor 325 times more potent at the CB1 receptor compared with the CB2 receptor induces hypothermia in mice with the same efficacy as AEA, in