Dihydrogossypetin
Names
IUPAC name
(2R,3R)-3,3′,4′,5,7,8-Hexahydroxyflavan-4-one
Systematic IUPAC name
(2R,3R)-2-(3,4-Dihydroxyphenyl)-3,5,7,8-tetrahydroxy-2,3-dihydro-4H-1-benzopyran-4-one
Other names
2,3-Dihydrogossypetin
3′,4′,5,7,8-pentahydroxyflavanonol
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
UNII
  • InChI=1S/C15H12O8/c16-6-2-1-5(3-7(6)17)14-13(22)12(21)10-8(18)4-9(19)11(20)15(10)23-14/h1-4,13-14,16-20,22H/t13-,14+/m0/s1 ☒N
    Key: ZHPLPRUARZZBET-UONOGXRCSA-N ☒N
  • InChI=1/C15H12O8/c16-6-2-1-5(3-7(6)17)14-13(22)12(21)10-8(18)4-9(19)11(20)15(10)23-14/h1-4,13-14,16-20,22H/t13-,14+/m0/s1
    Key: ZHPLPRUARZZBET-UONOGXRCBO
  • C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O)OC1=CC(=C(C=C1[C@@H]2C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O)O
Properties
C15H12O8
Molar mass 320.25 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Dihydrogossypetin is a flavanonol, a type of flavonoid.[1]

Biosynthesis

The enzyme Taxifolin 8-monooxygenase hydroxylates taxifolin using NADH, NADPH, H+, and O2 to produce 2,3-dihydrogossypetin, NAD+, NADP+, and H2O.


References

  1. ↑ Jeffrey, A. M.; Jerina, D. M.; Self, R.; Evans, W. C. (1972). "The bacterial degradation of flavonoids. Oxidative fission of the A-ring of dihydrogossypetin by a Pseudomonas sp". The Biochemical Journal. 130 (2): 383–90. doi:10.1042/bj1300383. PMC 1174417. PMID 4198081.


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