Naringenin chalcone

Naringenin chalcone
Names
Preferred IUPAC name
2′,4,4′,6′-Tetrahydroxychalcone
Other names
Chalconaringenin; Isosalipurpol
Identifiers
CAS Number
  • 25515-46-2 checkY
  • 73692-50-9 (non-specific) checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:15413
ChemSpider
  • 4444447
KEGG
  • C06561
PubChem CID
  • 5280960
UNII
  • YCF6Z24AS2 checkY
CompTox Dashboard (EPA)
  • DTXSID101043553 Edit this at Wikidata
InChI
  • InChI=1S/C15H12O5/c16-10-4-1-9(2-5-10)3-6-12(18)15-13(19)7-11(17)8-14(15)20/h1-8,16-17,19-20H/b6-3+
    Key: YQHMWTPYORBCMF-ZZXKWVIFSA-N
  • C1=CC(=CC=C1/C=C/C(=O)C2=C(C=C(C=C2O)O)O)O
Properties
Chemical formula
 C15H12O5
Molar mass 272.256 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
Chemical compound

Naringenin chalcone[1] is a common chalconoid (or chalcone, not to be confused with the compound chalcone). It is synthesized from 4-coumaroyl-CoA and malonyl-CoA by chalcone synthase (CHS), a key enzyme in the phenylpropanoid pathway. Naringenin chalcone can spontaneously cyclize to naringenin (a flavanone). In plant cells, this process is catalyzed by chalcone isomerase.

References

  1. ^ PubChem. "Naringenin chalcone". pubchem.ncbi.nlm.nih.gov. Retrieved 2022-08-27.


  • v
  • t
  • e