The amyrins are three closely related natural chemical compounds of the triterpene class. They are designated ñ-amyrin (ursane skeleton), ò-amyrin (oleanane skeleton), and ô-amyrin. Each is a pentacyclic triterpenol with the chemical formula C<sub>30</sub>H<sub>50</sub>O. They are widely distributed in nature and have been isolated from a variety of plant sources such as epicuticular wax. In plant biosynthesis, ñ-amyrin is the precursor of ursolic acid and ò-amyrin is the precursor of oleanolic acid. All three amyrins occur in the surface wax of tomato fruit. ñ-Amyrin is found in dandelion coffee.
A study demonstrated that ñ,ò-amyrin exhibits long-lasting antinociceptive and anti-inflammatory properties in 2 models of persistent nociception via activation of the cannabinoid receptors CB1 and CB2 and by inhibiting the production of cytokines and expression of NF-úB, CREB, and cyclooxygenase 2.