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Merck
CN

G7772

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
NACRES:
NA.25
PubChem Substance ID:
24895321
UNSPSC Code:
12352201
EC Number:
200-286-9
MDL number:
MFCD00136040

Key Documents

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InChI key

VFRROHXSMXFLSN-UHFFFAOYSA-N

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)

SMILES string

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

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

Quality Level

200

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.

Other Notes

Prepared from G 7879.
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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Regulatory Information

涉药品监管产品
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Certificates of Analysis (COA)

Lot/Batch Number
0000477244
0000477244
0000354458
0000354564
0000311383

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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
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
Fook-Choe Cheah et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 28(7), 3205-3210 (2014-03-19)
Erythrocytes require glucose-6-phosphate dehydrogenase (G6PD) to generate NADPH and protect themselves against hemolytic anemia induced by oxidative stress. Peroxiredoxin 2 (Prx2) is a major antioxidant enzyme that requires NADPH to recycle its oxidized (disulfide-bonded) form. Our aims were to determine
Glucose-6-phosphate reduces calcium accumulation in rat brain endoplasmic reticulum.
Cole, JT.
Frontiers in Neuroscience, 5, 51-51 (2012)
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