Curcumin: Difference between revisions

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== Curcumin ==
<gallery>
File:curcumin.svg|Curcumin
File:curcuminKeto.svg|Curcumin Keto
File:Curcumin-enol-3D-balls.png|Curcumin Enol 3D Balls
File:Curcumin-keto-3D-balls.png|Curcumin Keto 3D Balls
File:Kurkumina.jpg|Kurkumina
File:Curcumin_thin_lipid_film.jpg|Curcumin Thin Lipid Film
File:Curcumin_biosynthesis.svg|Curcumin Biosynthesis
File:Curcumin_fluorescence.jpg|Curcumin Fluorescence
</gallery>

Latest revision as of 21:32, 23 February 2025

Curcumin is a bright yellow chemical produced by some plants. It is the principal curcuminoid of turmeric (Curcuma longa), a member of the ginger family, Zingiberaceae. It is sold as an herbal supplement, cosmetics ingredient, food flavoring, and food coloring.

Chemical properties[edit]

Curcumin is a diarylheptanoid, belonging to the group of curcuminoids, which are natural phenols responsible for turmeric's yellow color. It is a tautomeric compound existing in enolic form in organic solvents and as a keto form in water.

Medical research[edit]

Laboratory and clinical research have not confirmed any medical usage for curcumin. It is difficult to study because it is both unstable and poorly bioavailable. It is unlikely to produce useful leads for drug development.

Pharmacokinetics[edit]

Curcumin incorporates several functional groups whose structure was first identified in 1910. The aromatic ring systems, which are phenols, are connected by two α,β-unsaturated carbonyl groups. The diketones form stable enols and are readily deprotonated to form enolates; the α,β-unsaturated carbonyl group is a good Michael acceptor and undergoes nucleophilic addition.

Safety[edit]

As a component of turmeric, curcumin is generally considered safe by the FDA.

See also[edit]

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PubMed
Wikipedia

Curcumin[edit]