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G1259

Sigma-Aldrich

α-D-Glucose 1-phosphate disodium salt hydrate

≥95%

Sinonimo/i:

α-D-Glucopyranose 1-phosphate, Cori ester

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About This Item

Formula condensata:
C6H11O9PNa2 · xH2O
Numero CAS:
56401-20-8
Peso molecolare:
304.10 (anhydrous basis)
Numero CE:
260-154-1
Numero MDL:
MFCD00150837
Codice UNSPSC:
12352201
ID PubChem:
24895053
NACRES:
NA.25

Origine biologica

synthetic

Saggio

≥95%

Stato

powder

Impurezze

glucose and starch, essentially free

Colore

white

Solubilità

water: 50 mg/mL, clear, colorless

Cationi in tracce

Na: 12.5-18.0% (anhydrous)

Attività estranea

α-D-glucose 1,6-diphosphate ~1% (usually sufficient to catalyze the assay of phosphoglucomutase)

Temperatura di conservazione

−20°C

Stringa SMILE

[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
YWAUQXHOCBBYLP-FBNUBEQJSA-L

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Descrizione generale

α-D-Glucose 1-phosphate is converted into D-glucose-6-phosphate by the enzyme phosphoglucomutase.
α-D-Glucose 1-phosphate is the α-anomeric form of glucose which contains a phosphate group on the primary carbon. It can be converted into the deoxysugar CDP-glucose by the enzyme α-D-Glucose-1-phosphate cytidylyltransferase.

Altre note

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

Codice della classe di stoccaggio

13 - Non Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
SLBR2458V
SLBG3566V
081M5306V
081M5306
128K3778

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Sigma-Aldrich

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Sigma-Aldrich

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D-Glucose 6-phosphate sodium salt

Stanley A Blumenthal
Perspectives in biology and medicine, 55(2), 236-249 (2012-05-31)
In 1945, Earl Sutherland (1915-1974) [corrected] and associates began studies of the mechanism of hormone-induced glycogen breakdown in the liver. In 1956, their efforts culminated in the identification of cyclic AMP, an ancient molecule generated in many cell types in
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
Achim Dickmanns et al.
Journal of molecular biology, 405(2), 461-478 (2010-11-16)
Nucleotide sugars and the enzymes that are responsible for their synthesis are indispensable for the production of complex carbohydrates and, thus, for elaboration of a protective cellular coat for many organisms such as the protozoan parasite Leishmania. These activated sugars
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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