Tremetone: Difference between revisions

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[[Category:Benzofurans]]
[[Category:Benzofurans]]
[[Category:Plant toxins]]
[[Category:Plant toxins]]
<gallery>
File:Tremetone_chemical_structure.svg|Chemical structure of Tremetone
File:Synthesis_(Racemate).png|Synthesis of Tremetone (Racemate)
File:Synthesis_(Enantiomeric).png|Synthesis of Tremetone (Enantiomeric)
</gallery>

Latest revision as of 01:40, 18 February 2025

A chemical compound found in certain plants


Chemical Compound
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PubChem CID
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UNII
ChEBI
ChEMBL
Properties
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GHS Pictograms [[File:|50px]]
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NFPA 704 [[File:|50px]]
References

Tremetone is a chemical compound that belongs to the class of benzofuran derivatives. It is notably found in certain species of the Asteraceae family, such as white snakeroot (Ageratina altissima). Tremetone is one of the compounds responsible for the toxic effects associated with these plants.

Chemical structure and properties[edit]

Tremetone is characterized by its benzofuran core structure. The chemical formula of tremetone is C13H12O3. The compound is a colorless solid under standard conditions. Its structure includes a benzene ring fused to a furan ring, with additional functional groups that contribute to its chemical properties.

Occurrence[edit]

Tremetone is primarily found in the white snakeroot plant, which is native to North America. This plant is known for its toxic properties, which were historically responsible for "milk sickness" in humans and animals. Milk sickness occurred when livestock consumed white snakeroot, and the toxin was passed to humans through milk and meat.

Toxicity[edit]

The toxicity of tremetone is attributed to its ability to interfere with metabolic processes in animals. When ingested, it can cause symptoms such as tremors, weakness, and in severe cases, death. The compound affects the mitochondria, disrupting energy production in cells.

Synthesis[edit]

The synthesis of tremetone can be achieved through several chemical pathways. The racemic mixture of tremetone can be synthesized using a series of organic reactions starting from simple precursors. The enantiomeric synthesis involves more complex steps to ensure the production of a specific optical isomer.

Synthesis of racemic tremetone
Synthesis of enantiomeric tremetone

Related pages[edit]

References[edit]

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