The utility of eugenol, a naturally occurring phenolic compound, for various applications is limited due to its
unfavorable properties. Thus, eugenyl acetate is under consideration as a substitute. The immunomodulatory activity of eugenyl
acetate compared to eugenol was investigated. Eugenyl acetate stimulated oxidative burst release from macrophages much more
than eugenol. Eugenol and eugenyl acetate similarly suppressed B-cell proliferation through the T-cell independent pathway, the
same as lipopolysaccharide, as well as the T-cell dependent pathway, the same as pokeweed mitogen. Eugenol effectively
stimulated T-cell proliferation more than eugenyl acetate through the same pathway as concanavalin A. Moreover, both eugenol
and eugenyl acetate showed similar maximal activity in inhibiting interferon γ (IFN-γ) and interleukin-2 (IL-2) production and
stimulating IL-10 secretion. Our findings suggested that eugenyl acetate might be used as a substitute for or accompany eugenol
as a potential therapeutic agent in treating inflammatory diseases and thereby decrease the potential high dose toxicity of eugenol.