Phytochemical studies on the leaves of Eucalyptus camaldulensis var. obtusa
have resulted in the isolation of a new triterpenoid camaldulin (3 beta-fo
rmyloxyurs-11-en-28,13 beta-olide) (1) along with ursolic acid lactone acet
ate (2), ursolic acid lactone (3), betulinic acid (4), and beta-sitosterol
3-O-beta-D-glucopyranoside (5). The structures were assigned on the basis o
f 1D and 2D NMR studies. Compounds 1-3 were tested for spasmolytic activity
and were found to possess calcium antagonist activity.