Zinc pyrithione is believed to have antiviral activity by acting as a zinc
ionophore, facilitating the transport of zinc cations across cellular membranes and into the cytoplasm. This increase in intracellular zinc levels has been shown to suppress viral replication within in vitro cell culture models across several viral families (including
coronaviruses,
coxsackieviruses, and
rhinoviruses) by interfering with RNA-dependent
RNA polymerase (RdRp) activity, inhibiting
RNA synthesis, and disrupting the proteolytic processing of viral nonstructural polyproteins. Beyond these effects, it appears to inhibits the expression of essential genes in certain viruses in vitro, specifically the
immediate early gene ICP4 and the late gene glycoprotein D (gD), effectively halting the viral life cycle at multiple stages. Zinc pyrithione also influences the cellular
ubiquitin-proteasome system (UPS) to degrade
IκBα, which prevents the activation of
NF-κB, a signaling pathway that viruses like
herpes simplex virus typically exploit to facilitate their own replication within the host cell. == See also ==