In the present study, we attempted to compare four petasins, isolated from Petasites formosanus Kitamura, and to look for structure-activity relationships, which may be helpful for synthesizing more active compounds for the treatment of asthma. Four petasins, including petasin, isopetasin, S-petasin and S-isopetasin, concentration-dependently relaxed histamine (10 muM)-, carbachol (0.2 muM)-, KCI (30 mM)-, and leukotriene D-4 (10 nM)-induced precontractions of isolated guinea pig tracheais. The IC50 Values strongly showed that the relaxant effects of the sulfur-containing petasins, S-petasin and S-isopetasin, were more potent than those of non-sulfur-containing petasins, petasin and isopetasin. S-Isopetasin, with IC50 Values around 10 muM, selectively relaxed carbachol- and KCI-induced precontractions, and had almost no effects (IC(50)s > 300 muM) on histamine- and leukotriene D-4-induced precontractions. However, 5-petasin, with IC50 values about 6 -9 muM, non-selectively relaxed the precontractions induced by all these contractile agents. The influence of isomerization of either petasin to isopetasin or S-petasin to S-isopetasin on the relaxant effects is not clear.