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G7250

Sigma-Aldrich

D-Glucose 6-phosphate disodium salt hydrate

≥98% (HPLC)

Sinônimo(s):

G-6-P-Na2, Robison ester

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About This Item

Fórmula empírica (Notação de Hill):
C6H11Na2O9P · xH2O
Número CAS:
Peso molecular:
304.10 (anhydrous basis)
Beilstein:
5199009
Número CE:
Número MDL:
Código UNSPSC:
12352201
ID de substância PubChem:
NACRES:
NA.25

fonte biológica

synthetic (organic)

Ensaio

≥98% (HPLC)

forma

powder

técnica(s)

HPLC: suitable

cor

white

solubilidade

water: 50 mg/mL, clear, colorless

traços de cátion

Na: 13.5-16.7% (anhydrous)

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

O.[Na+].[Na+].OC1O[C@H](COP([O-])([O-])=O)[C@@H](O)[C@H](O)[C@H]1O

InChI

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

chave InChI

UUWJZXLTPORJKW-WYFATIGWSA-L

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Aplicação

D-Glucose 6-phosphate disodium salt hydrate has been used as a component in the reaction mixture to assay reduced nicotinamide adenine dinucleotide phosphate (NADPH) diaphorase activity, NAD(P)H-cytochrome c reductase activity, and ferredoxin (Fd)-dependent cytochrome c reduction activity.

Ações bioquímicas/fisiológicas

D-Glucose 6-phosphate is the core carbohydrate substrate for the enzymatic synthesis of archaetidyl-myo-inositols produced through a pathway involving myo-inositol 1-phosphate synthase and CDP-archaeol.

Qualidade

usually 2-4 H2O/mole

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.

Código de classe de armazenamento

11 - Combustible Solids

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, Gloves, type N95 (US)


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Hiroyuki Morii et al.
The Journal of biological chemistry, 284(45), 30766-30774 (2009-09-11)
Ether-type inositol phospholipids are ubiquitously distributed in Archaea membranes. The present paper describes a novel biosynthetic pathway of the archaeal inositol phospholipid. To study the biosynthesis of archaetidylinositol in vitro, we prepared two possible substrates: CDP-archaeol, which was chemically synthesized
Federica Pisaneschi et al.
Molecules (Basel, Switzerland), 24(13) (2019-07-22)
We recently reported that SF2312 ((1,5-dihydroxy-2-oxopyrrolidin-3-yl)phosphonic acid), a phosphonate antibiotic with a previously unknown mode of action, is a potent inhibitor of the glycolytic enzyme, Enolase. SF2312 can only be synthesized as a racemic-diastereomeric mixture. However, co-crystal structures with Enolase
Khosbayar Lkhagvadorj et al.
International journal of molecular sciences, 22(1) (2020-12-31)
Prenatal smoke exposure (PreSE) is a risk factor for nicotine dependence, which is further enhanced by postnatal smoke exposure (PostSE). One susceptibility gene to nicotine dependence is Cytochrome P450 (CYP) 2A6, an enzyme responsible for the conversion of nicotine to
Khosbayar Lkhagvadorj et al.
Epigenetics, 15(12), 1370-1385 (2020-06-24)
Prenatal smoke exposure (PSE) is a risk factor for nicotine dependence. One susceptibility gene for nicotine dependence is Cytochrome P450 (CYP) 2A6, an enzyme responsible for the conversion of nicotine to cotinine and nicotine clearance in the liver. Higher activity
Daisuke Seo et al.
Biochimica et biophysica acta, 1794(4), 594-601 (2009-01-24)
Ferredoxin-NADP(+) oxidoreductases (FNRs) of Bacillus subtilis (YumC) and Rhodopseudomonas palustris CGA009 (RPA3954) belong to a novel homo-dimeric type of FNR with high amino acid sequence homology to NADPH-thioredoxin reductases. These FNRs were purified from expression constructs in Escherichia coli cells

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