Lucanthone
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Lucanthone is a chemical compound that was initially developed as an antischistosomal agent. It is a thioxanthone derivative and was used in the mid-20th century for the treatment of schistosomiasis, a disease caused by parasitic worms.
History[edit | edit source]
Lucanthone was first synthesized in the 1940s by the pharmaceutical industry as a potential treatment for schistosomiasis. It was one of the first drugs to be used for this purpose, and it was widely used until the 1980s when it was replaced by praziquantel, a more effective and safer drug.
Mechanism of Action[edit | edit source]
The exact mechanism of action of lucanthone is not fully understood. However, it is believed to work by inhibiting the DNA repair mechanisms of the schistosome parasite, leading to its death. It is also thought to interfere with the parasite's ability to metabolize glucose, which is essential for its survival.
Side Effects and Safety[edit | edit source]
Lucanthone is known to have several side effects, including nausea, vomiting, and abdominal pain. It can also cause more serious side effects such as liver damage and neurotoxicity. Due to these side effects and the development of safer alternatives, lucanthone is no longer widely used in the treatment of schistosomiasis.
Current Research[edit | edit source]
Despite its drawbacks, lucanthone has recently attracted interest as a potential anticancer agent. Some studies have suggested that it may be effective in treating certain types of brain tumors, although more research is needed in this area.
See Also[edit | edit source]
References[edit | edit source]
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Contributors: Prab R. Tumpati, MD