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Aurone

Names
IUPAC name 2-Benzylidene-1-benzofuran-3-one
Identifiers
CAS Number	582-04-7
3D model (JSmol)	Interactive image
ChemSpider	533325
PubChem CID	613552
CompTox Dashboard (EPA)	DTXSID70424870
InChI InChI=1S/C15H10O2/c16-15-12-8-4-5-9-13(12)17-14(15)10-11-6-2-1-3-7-11/h1-10HKey: OMUOMODZGKSORV-UHFFFAOYSA-N InChI=1/C15H10O2/c16-15-12-8-4-5-9-13(12)17-14(15)10-11-6-2-1-3-7-11/h1-10HKey: OMUOMODZGKSORV-UHFFFAOYAF
SMILES C1=CC=C(C=C1)C=C2C(=O)C3=CC=CC=C3O2
Properties
Chemical formula	C15H10O2
Molar mass	222.243 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is  ?) Infobox references

Aurone is a heterocyclic chemical compound which is a type of flavonoid. There are two isomers of the molecule, with (E)- and (Z)-configurations. The molecule contains a benzofuran element associated with a benzylidene linked in position 2. In aurone, a chalcone-like group is closed into a 5-membered ring instead of the 6-membered ring more typical of flavonoids.

Aurone forms the core for a family of derivatives which are known collectively as aurones. Aurones are plant flavonoids that provide yellow color to the flowers of some popular ornamental plants, such as snapdragon and cosmos. Aurones including 4'-chloro-2-hydroxyaurone (C₁₅H₁₁O₃Cl) and 4'-chloroaurone (C₁₅H₉O₂Cl) can also be found in the brown alga Spatoglossum variabile.

Most aurones are in a (Z)-configuration, which is the more stable configuration according to Austin Model 1 computation, but there are also some in the (E)-configurations such as (E)-3'-O-β-d-glucopyranosyl-4,5,6,4'-tetrahydroxy-7,2'-dimethoxyaurone, found in Gomphrena agrestis.

Analogy with flavonoids suggests that aurones could have interesting biological properties.

Related compound examples

• Aureusidin
• Hispidol (6,4'-Dihydroxyaurone)
• Leptosidin
• Sulfuretin (6,3',4'-Trihydroxyaurone)
• 4,5,6-Trihydroxyaurone

Metabolism

• Aureusidin synthase

References

1. Nakayama, T (2002). "Enzymology of aurone biosynthesis". Journal of Bioscience and Bioengineering. 94 (6): 487. doi:10.1016/S1389-1723(02)80184-0. PMID 16233339.
2. ^ Nakayama, T; Sato, T; Fukui, Y; Yonekura-Sakakibara, K; Hayashi, H; Tanaka, Y; Kusumi, T; Nishino, T (2001). "Specificity analysis and mechanism of aurone synthesis catalyzed by aureusidin synthase, a polyphenol oxidase homolog responsible for flower coloration". FEBS letters. 499 (1–2): 107–11. doi:10.1016/S0014-5793(01)02529-7. PMID 11418122.
3. ^ Atta-Ur-Rahman; Choudhary, MI; Hayat, S; Khan, AM; Ahmed, A (2001). "Two new aurones from marine brown alga Spatoglossum variabile". Chemical & pharmaceutical bulletin. 49 (1): 105–7. doi:10.1248/cpb.49.105. PMID 11201212.
4. Ferreira, EO; Salvador, MJ; Pral, EM; Alfieri, SC; Ito, IY; Dias, DA (2004). "A new heptasubstituted (E)-aurone glucoside and other aromatic compounds of Gomphrena agrestis with biological activity" (PDF). Zeitschrift fur Naturforschung. C, Journal of biosciences. 59 (7–8): 499–505. PMID 15813368.
5. Villemin, Didier; Martin, Benoit; Bar, Nathalie (1998). "Application of Microwave in Organic Synthesis. Dry Synthesis of 2-Arylmethylene-3(2)-naphthofuranones". Molecules. 3: 88. doi:10.3390/30300088.{{cite journal}}: CS1 maint: unflagged free DOI (link)
6. Hispidol on metabolomics.jp

• Aurones