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G7772

Sigma-Aldrich

D-Glucose 6-phosphate solution

~1 M in H2O (approx. 260 mg per ml)

Synonym(s):

D(+)-Glucopyranose 6-phosphate, Robison ester

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About This Item

Empirical Formula (Hill Notation):
C6H13O9P
CAS Number:
56-73-5
Molecular Weight:
260.14
EC Number:
200-286-9
MDL number:
MFCD00136040
UNSPSC Code:
12352201
PubChem Substance ID:
24895321
NACRES:
NA.25

biological source

synthetic (inorganic)

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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Related Categories

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
GHS05

signalword

Danger

hcodes

H314

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

Certificates of Analysis (COA)

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Victor V Lemeshko
Biochimica et biophysica acta, 1838(5), 1362-1371 (2014-01-15)
The simplest mechanism of the generation of the mitochondrial outer membrane potential (OMP) by the VDAC (voltage-dependent anion channel)-hexokinase complex (VHC), suggested earlier, and by the VDAC-glucokinase complex (VGC), was computationally analyzed. Even at less than 4% of VDACs bound
C Kern et al.
Insect molecular biology, 21(4), 456-471 (2012-07-06)
Trehalose phosphate synthase (EC 2.4.1.15; TPS) is the crucial enzyme for the biosynthesis of trehalose, the main haemolymph sugar of insects, and therefore a potential insecticidal molecular target. In this study, we report the functional heterologous expression of Drosophila melanogaster
Gang Zhao et al.
Biomedical chromatography : BMC, 28(7), 947-956 (2013-12-21)
In this study, a simple and sensitive gas chromatography-mass spectrometry method was developed for the study of bioavailability and protein binding and the metabolism of imperatorin in rat. The results showed that the pharmacokinetics of imperatorin after intravenous and oral
Stephen M Ansell et al.
Mayo Clinic proceedings, 87(6), 571-580 (2012-06-09)
The use of sensitive and specific imaging techniques for accurate initial staging and evaluation of response to therapy in patients with lymphoma is essential for their optimal management. Fluorine 18 fluorodeoxyglucose (FDG) positron emission tomography (PET) integrated with computed tomography
Tomoaki Yamamotoya et al.
Biochimica et biophysica acta, 1824(12), 1442-1448 (2012-07-04)
In the studies of Escherichia coli (E. coli), metabolomics analyses have mainly been performed using steady state culture. However, to analyze the dynamic changes in cellular metabolism, we performed a profiling of concentration of metabolites by using batch culture. As
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