The rhizomes of Ferula communis yielded three antibacterial sesquiterp
enes, namely, the new daucane ester 14-(o-hydroxycinnamoyloxy)-dauc-4,
8-diene (1), ferulenol (2) and ferchromone (3). Compound 1 exhibited s
ignificant activity against Gram-positive bacteria, while 3 was found
to be less active. Compound 2, on the other hand, demonstrated potent
activity against Mycobacterium organisms, and its corresponding C-4-ac
etoxy derivative 9 was found to retain the same activity as well. In a
ddition, the rhizomes yielded a number of inactive compounds, includin
g 2-nor-1,2-secoferulenol, elemicin, colladonin, feselol and compounds
4 and 5. Structural assignments were largely based on the spectral da
ta, especially the 2D NMR COSY and HETCOR experiments. (C) 1998 John W
iley & Sons, Ltd.