Table 1.
FDA approved and experimental drugs targeting copper metabolism in cancer treatment.
Drug Name | Mechanism | FDA Approval Status | Disease |
---|---|---|---|
D-penicillamine | Binds to copper and leads to its excretion | Yes | Wilson’s disease |
Trientine | Binds to copper and leads to its excretion | Yes | Wilson’s disease |
Zinc acetate | Blocks absorption of copper in the gut | Yes | Wilson’s disease |
Tetrathiomolybdate | Binds to copper and leads to its excretion | No | N/A |
Ethylenediaminetetraacetic acid (EDTA) | Binds to copper and leads to its excretion | Yes | Lead poisoning and iron overload |
Dimercapto-propane sulfonate (DMPS) | Binds to copper and leads to its excretion | No | N/A |
Dimercaptosuccinic acid (DMSA) | Binds to copper and leads to its excretion | Yes | Lead poisoning in children |
Disulfiram (DSF) | Transports copper into cells and leads to its overload | Yes | Alcoholism |
Elesclomol | Transports copper into cells and leads to its overload | No | N/A |
Diacetyl-bis (N4-methylthiosemicarbazone) (ATSM) | Transports copper into cells and leads to its overload | No | N/A |
Glyoxal-bis (N4-methylthiosemicarbazone) (GTSM) | Transports copper into cells and leads to its overload | No | N/A |
N/A, Not applicable.