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G7772

Sigma-Aldrich

D-Glucose 6-phosphate solution

~1 M in H2O (approx. 260 mg per ml)

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Synonym(s):
D(+)-Glucopyranose 6-phosphate, Robison ester
Empirical Formula (Hill Notation):
C6H13O9P
CAS Number:
Molecular Weight:
260.14
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.25

biological source

synthetic (inorganic)

Quality Level

assay

≥99% (TLC)

form

liquid

concentration

~1 M in H2O (approx. 260 mg per ml)

technique(s)

thin layer chromatography (TLC): suitable

color

colorless

shipped in

dry ice

storage temp.

−20°C

SMILES string

OC(COP(O)(O)=O)C(O)C(O)C(O)C=O

InChI

1S/C6H13O9P/c7-1-3(8)5(10)6(11)4(9)2-15-16(12,13)14/h1,3-6,8-11H,2H2,(H2,12,13,14)

InChI key

VFRROHXSMXFLSN-UHFFFAOYSA-N

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Application


  • Phosphonate and α-fluorophosphonate analogs of d-glucose 6-phosphate as active-site probes of 1l-myo-inositol 1-phosphate synthase.: This study explores phosphonate and α-fluorophosphonate analogs of d-glucose 6-phosphate, offering insights into their use as probes for understanding enzyme mechanisms, which could impact biochemical research methodologies (Ramos-Figueroa et al., 2023).

Biochem/physiol Actions

D-Glucose 6-phosphate binds and inhibits the activity of sarcoendoplasmic reticulum calcium ATPase in rat brains resulting in a decrease in the accumulation of calcium in the endoplasmic reticulum.

Linkage

Prepared from G 7879.

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible, corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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