Zinc Ionophores

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Zinc ionophores are compounds that bind on zinc, and transport the extracellular Zn2+ ions across the cell membrane, and are researched for their anticancer and antiviral tendencies.[1][2] Examples of Zinc Ionophores are Hinokitiol (HK) and Pyrithione (PT) and have been found to inhibit human mengovirus, rhinovirus, and coxsackievirus multiplication effectively.[3] Chloroquine has also been identified as a Zinc Ionophore that portrays its anticancer capability, and it has been considered as a potential anticancer agent.[4]

Antiviral Activity

Zinc Ionophores, Hinokitiol, and Pyrithione are useful in the inhibition of Picornavirus replication through the interference with the viral polyprotein proper processing.[5] Hinokitiol and Pyrithione also result in a swift importation of extracellular Zn2+ ions into the cells, which increases the inhibition against Picornavirus infection.[6]

Anticancer Activity

The ability to bind on Zinc ions allows Zinc ionophores to cause apoptosis within cancer cells.[7] Zinc Ionophores kill cancer cells via ways such as proteasome inhibition and lysosomal disruption, and thus, have proven to be potential anticancer agents.[8]

References