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// Workers AI · dad joke modeWhat did Combretol say to its date? You comb ine well with me.

From Wikipedia, the free encyclopedia
Combretol
Chemical structure of combretol
Chemical structure of combretol
Names
IUPAC name
5-Hydroxy-3,3′,4′,5′,7-pentamethoxyflavone
Preferred IUPAC name
5-Hydroxy-3,7-dimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-1-benzopyran-4-one
Other names
3,7,3',4',5'-pentamethylmyricetin
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
UNII
  • InChI=1S/C20H20O8/c1-23-11-8-12(21)16-13(9-11)28-18(20(27-5)17(16)22)10-6-14(24-2)19(26-4)15(7-10)25-3/h6-9,21H,1-5H3 X markN
    Key: SUNUQCQIFHHEOW-UHFFFAOYSA-N X markN
  • InChI=1/C20H20O8/c1-23-11-8-12(21)16-13(9-11)28-18(20(27-5)17(16)22)10-6-14(24-2)19(26-4)15(7-10)25-3/h6-9,21H,1-5H3
    Key: SUNUQCQIFHHEOW-UHFFFAOYAT
  • COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)OC)OC)OC)O
Properties
C20H20O8
Molar mass 388.36 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X markN verify (what is checkYX markN ?)

Combretol is an O-methylated flavonol, a type of flavonoid. It is the 3,7,3',4',5'-O-methylation of myricetin and can be extracted from Combretum quadrangulare[2] and from Rhodomyrtus tomentosa.[3]

References

[edit]
  1. "KNApSAcK Metabolite Information - C00004777". www.knapsackfamily.com.
  2. Combretol from Combretum quadrangulare. Stang Mongkolsuk, F. M. Dean and L. E. Houghton, J. Chem. Soc. C, 1966, page 125, doi:10.1039/J39660000125
  3. 5-Hydroxy-3,3',4',5',7-pentamethoxyflavone (combretol). Dachriyanus, R. Fahmi, M. V. Sargent, B. W. Skelton and A. H. White, Acta Crystallogr. (2004). E60, o86-o88