Luteoliflavan

Luteoliflavan

File:Luteoliflavan.svg
Names
IUPAC name (2S)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-5,7-diol
Other names 3',4',5,7-tetrahydroxyflavan
Identifiers
CAS Number	446-06-0 checkY
3D model (JSmol)	Interactive image
ChEBI	CHEBI:29620
ChemSpider	558684 checkY
ECHA InfoCard
E number
KEGG	C12122
PubChem CID	643542
CompTox Dashboard (EPA)	DTXCID50300289
InChI 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
SMILES C1CC2=C(C=C(C=C2OC1C3=CC(=C(C=C3)O)O)O)O
Properties
Chemical formula	C15H14O5
Molar mass	274.272 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

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

Uses

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