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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
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biological source

synthetic (inorganic)

Quality Level

200

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

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
0000542452
0000542453
0000542453
0000542452
0000477244

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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
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
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
Glucose-6-phosphate reduces calcium accumulation in rat brain endoplasmic reticulum.
Cole, JT.
Frontiers in Neuroscience, 5, 51-51 (2012)
Tiffany R Bonnett et al.
Insect biochemistry and molecular biology, 42(12), 890-901 (2012-09-18)
Mountain pine beetles, Dendroctonus ponderosae Hopkins (Coleoptera: Curculionidae), are native to western North America, but have recently begun to expand their range across the Canadian Rocky Mountains. The requirement for larvae to withstand extremely cold winter temperatures and potentially toxic
View All Related Papers

Global Trade Item Number

SKUGTIN
G7772-500MG04061833643174
G7772-5G04061833643181
G7772-1G04061838172907

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