Following an earlier demonstration of an antiviral effect against vari
cella-zoster virus (VZV, human herpesvirus 3) using 2-hydroxymyristic
acid (2-hydroxytetradecanoic acid; 2-HM), an inhibitor of protein myri
stoylation, both 2-HM and 2-hydroxypalmitic acid (2-hydroxyhexadecanoi
c acid; 2-HP) have been tested against a range of viruses. Although bo
th compounds inhibit the replication of varicella-zoster virus (VZV; h
uman herpesvirus 3) they do not inhibit the replication of closely rel
ated herpesviruses. They do, however, inhibit the replication of both
poliovirus (a member of the Picornaviridae) and the human immunodefici
ency virus type 1 (HIV-1; a member of the Retroviridae), Neither compo
und is toxic to adherent cells by dye uptake assay, although limited t
oxicity is apparent to non-adherent cell lines at high concentrations,
The mechanisms underlying these effects are discussed, A diminished e
ffect of 2-hydroxymyristic acid when the compound is dissolved in dime
thyl sulphoxide (DMSO) rather than ethanol is reported, and the implic
ations for the use of DMSO as a 'universal solvent' for compound scree
ning noted. Finally, it is suggested that targeting of 'virus-essentia
l' cellular functions may provide an alternative route for inhibiting
viral replication.