Merck
Todas las fotos(6)

Documentos

G7000

Sigma-Aldrich

α-D-Glucose 1-phosphate disodium salt hydrate

≥97%

Todas las fotos(6)
Sinónimos:
α-D-Glucopyranose 1-phosphate, Cori ester
Fórmula lineal:
C6H11O9PNa2 · xH2O
Número de CAS:
56401-20-8
Peso molecular:
304.10 (anhydrous basis)
Número de EC:
260-154-1
Número MDL:
MFCD00150837
ID de la sustancia en PubChem:
24895281
NACRES:
NA.25

origen biológico

synthetic

Nivel de calidad

200

Análisis

≥97%

formulario

powder

impurezas

≤0.1 mol % glucose
≤0.5 mol % α-D-glucose 1,6-diphosphate

color

white

solubilidad

water: 50 mg/mL, clear, colorless

trazas de catión

Na: 13.5-16.7% (anhydrous)

application(s)

agriculture

temp. de almacenamiento

−20°C

SMILES string

[Na+].[Na+].[H]O[H].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C6H13O9P.2Na.H2O/c7-1-2-3(8)4(9)5(10)6(14-2)15-16(11,12)13;;;/h2-10H,1H2,(H2,11,12,13);;;1H2/q;2*+1;/p-2/t2-,3-,4+,5-,6-;;;/m1.../s1

InChI key

YWAUQXHOCBBYLP-FBNUBEQJSA-L

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Este artículo
G7018G1259G6875
α-D-Glucose 1-phosphate disodium salt hydrate ≥97%

Sigma-Aldrich

G7000

α-D-Glucose 1-phosphate disodium salt hydrate

α-D-Glucose 1-phosphate disodium salt hydrate ≥98%, BioXtra, lyophilized powder

Sigma-Aldrich

G7018

α-D-Glucose 1-phosphate disodium salt hydrate

α-D-Glucose 1-phosphate disodium salt hydrate ≥95%

Sigma-Aldrich

G1259

α-D-Glucose 1-phosphate disodium salt hydrate

α-D-Glucose 1-phosphate dipotassium salt hydrate ≥97%

Sigma-Aldrich

G6875

α-D-Glucose 1-phosphate dipotassium salt hydrate

assay

≥97%

assay

≥98%

assay

≥95%

assay

≥97%

form

powder

form

lyophilized powder

form

powder

form

powder

impurities

≤0.1 mol % glucose, ≤0.5 mol % α-D-glucose 1,6-diphosphate

impurities

glucose, starch, and ethanol, essentially free, 0.01-0.2% α-D-glucose 1,6-diphosphate

impurities

glucose and starch, essentially free

impurities

glucose, essentially free

color

white

color

white

color

white

color

white

solubility

water: 50 mg/mL, clear, colorless

solubility

water: 50 mg/mL, clear

solubility

water: 50 mg/mL, clear, colorless

solubility

water: slightly soluble 50 g/L

Descripción general

α-D-Glucose 1-phosphate is converted into D-glucose-6-phosphate by the enzyme phosphoglucomutase.

Acciones bioquímicas o fisiológicas

Glucose-1-phosphate (G1P) is produced from glycogen during glycogenolysis by the actions of glycogen phosphorylase. Conversion to glucose-6-phosphate (G6P) by phosphoglucomutase allows for entry of the glucose molecule into metabolic pathways such as glycolysis. During glycogenesis, G6P is converted to G1P by the actions of phosphoglucose isomerase.

Nota de preparación

Prepared by a modification of the procedure of McCready, R.M., et al., J. Am. Chem. Soc., 66, 560 (1944).

Código de clase de almacenamiento

11 - Combustible Solids

WGK

WGK 3

Punto de inflamabilidad F

Not applicable

Punto de inflamabilidad C

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)

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Las referencias de los producto se combinan con los tamaños de envase y las cantidades cuando se muestran en la página web, por ejemplo: T1503-25G. Asegúrese de introducir el número de producto ÚNICAMENTE en el campo del Número de producto (Ejemplo T1503).

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T1503
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Glucose-6-phosphate mol wt (glucose-6-P: Mr = 260.2, glucose-6-P-Na2: Mr = 304.2), pkg of 5 g

Roche

10127647001

Glucose-6-phosphate

α-D-Glucose 1,6-bisphosphate tetra(cyclohexylammonium) salt hydrate ≥95%

Sigma-Aldrich

G5875

α-D-Glucose 1,6-bisphosphate tetra(cyclohexylammonium) salt hydrate

Jef Van der Borght et al.
Biotechnology journal, 5(9), 986-993 (2010-08-28)
β-D-Glucose-1-phosphate (βGlc1P) is an efficient glucosyl donor for both enzymatic and chemical glycosylation reactions but is currently very costly and not available in large amounts. This article provides an efficient production method of βGlc1P from trehalose and phosphate using the
Ting Yang et al.
The Biochemical journal, 429(3), 533-543 (2010-05-21)
The diverse types of glycoconjugates synthesized by trypanosomatid parasites are unique compared with the host cells. These glycans are required for the parasite survival, invasion or evasion of the host immune system. Synthesis of those glycoconjugates requires a constant supply
Kyra-Melinda Alexacou et al.
Bioorganic & medicinal chemistry, 18(22), 7911-7922 (2010-10-16)
Glycogen phosphorylase (GP) is a promising target for the treatment of type 2 diabetes. In the process of structure based drug design for GP, a group of 15 aromatic aldehyde 4-(β-d-glucopyranosyl)thiosemicarbazones have been synthesized and evaluated as inhibitors of rabbit
Joerg Fettke et al.
Plant physiology, 155(4), 1723-1734 (2010-12-01)
Almost all glucosyl transfer reactions rely on glucose-1-phosphate (Glc-1-P) that either immediately acts as glucosyl donor or as substrate for the synthesis of the more widely used Glc dinucleotides, ADPglucose or UDPglucose. In this communication, we have analyzed two Glc-1-P-related
Daniel Decker et al.
Phytochemistry, 79, 39-45 (2012-05-04)
UDP-Glc pyrophosphorylase (UGPase) is an essential enzyme responsible for production of UDP-Glc, which is used in hundreds of glycosylation reactions involving addition of Glc to a variety of compounds. In this study, barley UGPase was characterized with respect to effects
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