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Fructose 6-phosphate

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Fructose 6-phosphate
Names
IUPAC names
methoxyphosphonic acid
Other names β-D-fructose 6-phosphate,
fructose 6-phosphate
Identifiers
CAS Number
3D model (JSmol)
Abbreviations F6P
ChemSpider
ECHA InfoCard 100.010.360 Edit this at Wikidata
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C6H13O9P/c7-2-6(10)5(9)4(8)3(15-6)1-14-16(11,12)13/h3-5,7-10H,1-2H2,(H2,11,12,13)/t3-,4-,5+,6+/m1/s1Key: BGWGXPAPYGQALX-ZXXMMSQZSA-N
  • InChI=1/C6H13O9P/c7-2-6(10)5(9)4(8)3(15-6)1-14-16(11,12)13/h3-5,7-10H,1-2H2,(H2,11,12,13)/t3-,4-,5+,6+/m1/s1Key: BGWGXPAPYGQALX-ZXXMMSQZBI
SMILES
  • O=P(O)(O)OC1O(O)(CO)(O)1O
Properties
Chemical formula C6H13O9P
Molar mass 260.14 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

Fructose 6-phosphate (also known as the Neuberg ester) is fructose sugar phosphorylated on carbon 6 (i.e., is a fructosephosphate). The β-D-form of this compound is very common in cells. The vast majority of glucose and fructose entering a cell will become converted to this at some point. The name Neuberg ester comes from the German biochemist Carl Neuberg.

History

In 1918, Carl Neuberg found that the compound (only later identified as fructose 6-phosphate) could be produced by mild acid hydrolysis of "Harden-Young ester" (fructose 2,6-bisphosphate).

Fructose 6-phosphate in glycolysis

Fructose 6-phosphate lies within the glycolysis metabolic pathway and is produced by isomerisation of glucose 6-phosphate. It is in turn further phosphorylated to fructose-1,6-bisphosphate.

Template:Biochemical Reaction Compound C00668 at KEGG Pathway Database. Enzyme 5.3.1.9 at KEGG Pathway Database. Compound C05345 at KEGG Pathway Database. Enzyme 2.7.1.11 at KEGG Pathway Database. Enzyme 3.1.3.11 at KEGG Pathway Database. Reaction at KEGG Pathway Database. Compound C05378 at KEGG Pathway Database.

See also

Glycolysis metabolic pathway

Glucose

Hexokinase

ATP ADP Rightward reaction arrow with minor substrate(s) from top left and minor product(s) to top right

Glucose 6-phosphate

Glucose-6-phosphate
isomerase

Reversible left-right reaction arrow

Fructose 6-phosphate

Phosphofructokinase-1

ATP ADP Rightward reaction arrow with minor substrate(s) from top left and minor product(s) to top right

Fructose 1,6-bisphosphate

Fructose-bisphosphate
aldolase

Reversible left-right reaction arrow

Dihydroxyacetone phosphate

+

+

Glyceraldehyde 3-phosphate

Triosephosphate
isomerase

Reversible left-right reaction arrow

2 × Glyceraldehyde 3-phosphate

2 × 

Glyceraldehyde-3-phosphate
dehydrogenase

NAD+ Pi NADH + H Reversible left-right reaction arrow with minor forward substrate(s) from top left, minor forward product(s) to top right, minor reverse substrate(s) from bottom right and minor reverse product(s) to bottom leftNAD+ Pi NADH + H

2 × 1,3-Bisphosphoglycerate

2 × 

Phosphoglycerate kinase

ADP ATP Reversible left-right reaction arrow with minor forward substrate(s) from top left, minor forward product(s) to top right, minor reverse substrate(s) from bottom right and minor reverse product(s) to bottom leftADP ATP

2 × 3-Phosphoglycerate

2 × 

Phosphoglycerate mutase

Reversible left-right reaction arrow

2 × 2-Phosphoglycerate

2 × 

Phosphopyruvate
hydratase
(enolase)

  H2O Reversible left-right reaction arrow with minor forward product(s) to top right and minor reverse substrate(s) from bottom right  H2O

2 × Phosphoenolpyruvate

2 × 

Pyruvate kinase

ADP ATP Rightward reaction arrow with minor substrate(s) from top left and minor product(s) to top right

2 × Pyruvate

2 × 

References

  1. Fruton, Joseph S. Proteins, Enzymes, Genes: The Interplay of Chemistry and Biology. Yale University Press: New Haven, 1999. p 292
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