Luteoliflavan

In the world of Luteoliflavan, there are endless aspects to discover and explore. From its origins to its relevance today, Luteoliflavan has captured the attention of millions of people around the world. Whether through its influence on popular culture, its impact on society or its importance in times past, Luteoliflavan continues to spark interest and generate debate. In this article, we will delve into the fascinating world of Luteoliflavan, exploring its different facets and unraveling its meaning in the current context. From its evolution over the years to its role in people's lives, Luteoliflavan is a topic that deserves to be analyzed from various perspectives to understand its true magnitude.

Luteoliflavan
Names
IUPAC name
(2S)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-5,7-diol
Other names
3',4',5,7-tetrahydroxyflavan
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
  • InChI=1S/C15H14O5/c16-9-6-12(18)10-2-4-14(20-15(10)7-9)8-1-3-11(17)13(19)5-8/h1,3,5-7,14,16-19H,2,4H2/t14-/m0/s1 checkY
    Key: GWCPBEMISACTHQ-AWEZNQCLSA-N checkY
  • C1CC2=C(C=C(C=C2OC1C3=CC(=C(C=C3)O)O)O)O
Properties
C15H14O5
Molar mass 274.272 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).

Luteoliflavan is a flavan, a type of neoflavonoid (a polyphenolic compound).[1] Its chemical formula is C15H14O5. The compound has been found in Malus domestica, Malus pumila, and Camellia sinensis.[2][3] Luteoliflavan is a tetrahydroxyflavan, in which the four hydroxy groups are located at positions 3', 4', 5, and 7.[4] The compound plays a role as a plant metabolite.

Synthesis

Luteoliflavan can be prepared via both natural biosynthetic pathways in plants and synthetic organic chemistry methods.[5]

Uses

Luteoliflavan offers diverse biological activities that have led to its exploration in various medical applications: cancer therapy, diabetes management, neurological disorders.[6]

References

  1. ^ "NP-MRD: Showing NP-Card for luteoliflavan (NP0144784)". np-mrd.org. Retrieved 3 April 2025.
  2. ^ Daayf, Fouad; Lattanzio, Vincenzo (21 January 2009). Recent Advances in Polyphenol Research, Volume 1. John Wiley & Sons. p. 221. ISBN 978-1-4443-0241-7. Retrieved 3 April 2025.
  3. ^ Roemmelt, Susanne; Zimmermann, Norbert; Rademacher, Wilhelm; Treutter, Dieter (1 October 2003). "Formation of novel flavonoids in apple (Malus×domestica) treated with the 2-oxoglutarate-dependent dioxygenase inhibitor prohexadione-Ca". Phytochemistry. 64 (3): 709–716. doi:10.1016/S0031-9422(03)00389-3. ISSN 0031-9422. Retrieved 3 April 2025.
  4. ^ Kuete, Victor (19 June 2013). Medicinal Plant Research in Africa: Pharmacology and Chemistry. Newnes. p. 491. ISBN 978-0-12-405936-8. Retrieved 4 April 2025.
  5. ^ "Buy Luteoliflavan | 446-06-0". Smolecule. Retrieved 4 April 2025.
  6. ^ "Buy Luteoliflavan | 446-06-0 | BenchChem". benchchem.com. Retrieved 3 April 2025.


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