This study examined the inhibitory effects of trans-cinnamaldehyde (CA), an
aromatic aldehyde derived from Cinnamomi Cortex, on Saccharomyces cerevisi
ae cell wall synthesizing enzymes in vitro. This compound was found to be a
noncompetitive inhibitor of beta-(1,3)-glucan synthase and a mixed inhibit
or of chitin synthase 1 with 50% inhibitory concentrations (IC50) of 0.84 a
nd 1.44 mM, respectively. Chitin synthases 2 and 3 were less sensitive than
chitin synthase 1 to CA. CA can be useful as a model compound of cell wall
inhibitors for the development of effective antifungal agents.