Names | |
---|---|
IUPAC name 3′,4′,5,7-Tetrahydroxyflavone | |
Systematic IUPAC name 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one | |
Other names Luteolol Digitoflavone Flacitran Luteoline | |
Identifiers | |
3D model (JSmol) | |
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.007.038 |
KEGG | |
PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
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Properties | |
C15H10O6 | |
Molar mass | 286.239 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Luteolin is a flavone, a type of flavonoid, with a yellow crystalline appearance. [1]
Luteolin is the main yellow dye from the Reseda luteola plant, used for dyeing since at least the first millennium B.C. Luteolin was first isolated in pure form, and named, in 1829 by the French chemist Michel Eugène Chevreul. [2] [3] [4] The luteolin empirical formula was determined by the Austrian chemists Heinrich Hlasiwetz and Leopold Pfaundler in 1864. [5] [6] In 1896, the English chemist Arthur George Perkin proposed the correct structure for luteolin. [7] Perkin's proposed structure for luteolin was confirmed in 1900 when the Polish-Swiss chemist Stanislaw Kostanecki (1860–1910) and his students A. Różycki and J. Tambor synthesized luteolin. [8] [9]
Luteolin is most often found in leaves, but it is also present in rinds, barks, clover blossoms, and ragweed pollen. [1] It has also been isolated from the aromatic flowering plant, Salvia tomentosa in the mint family, Lamiaceae . [10]
Dietary sources include celery, broccoli, artichoke, green pepper, parsley, thyme, dandelion, perilla, chamomile tea, carrots, olive oil, peppermint, rosemary, navel oranges, and oregano. [11] [12] It can also be found in the seeds of the palm Aiphanes aculeata . [13]
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