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G7772

Sigma-Aldrich

D-Glucose 6-phosphate solution

~1 M in H2O (approx. 260 mg per ml)

Sinônimo(s):

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

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About This Item

Fórmula empírica (Notação de Hill):
C6H13O9P
Número CAS:
56-73-5
Peso molecular:
260.14
Número CE:
200-286-9
Número MDL:
MFCD00136040
Código UNSPSC:
12352201
ID de substância PubChem:
24895321
NACRES:
NA.25

fonte biológica

synthetic (inorganic)

Ensaio

≥99% (TLC)

forma

liquid

concentração

~1 M in H2O (approx. 260 mg per ml)

técnica(s)

thin layer chromatography (TLC): suitable

cor

colorless

Condições de expedição

dry ice

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

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)

chave InChI

VFRROHXSMXFLSN-UHFFFAOYSA-N

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Categorias relacionadas

Aplicação


  • 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).

Ações bioquímicas/fisiológicas

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.

Ligação

Prepared from G 7879.

Outras notas

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

Pictogramas

Corrosion
GHS05

Palavra indicadora

Danger

Frases de perigo

H314

Classificações de perigo

Skin Corr. 1B

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

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

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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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