F1502

D-Fructose 6-phosphate dipotassium salt

Name: <SC>D</SC>-Fructose 6-phosphate dipotassium salt
Brand: SIGMA

≥97% (enzymatic), amorphous powder

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Fórmula lineal:

C₆H₁₁O₉PK₂

Número CAS:

103213-47-4

Peso molecular:

336.32

MDL number:

MFCD30342368

UNSPSC Code:

12352201

PubChem Substance ID:

24894770

NACRES:

NA.25

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SMILES string

[K+].[K+].OCC1(O)O[C@H](COP([O-])([O-])=O)[C@@H](O)[C@@H]1O

InChI

1S/C6H13O9P.2K/c7-2-6(10)5(9)4(8)3(15-6)1-14-16(11,12)13;;/h3-5,7-10H,1-2H2,(H2,11,12,13);;/q;2*+1/p-2/t3-,4-,5+,6?;;/m1../s1

InChI key

UNAFCPBHNZYEIY-UHOQFTJOSA-L

biological source

synthetic (inorganic)

assay

≥97% (enzymatic)

form

amorphous powder

impurities

≤0.05 mol % fructose 1,6-diphosphate, ≤1.5 mol % glucose 6-phosphate

color

white to off-white

solubility

H₂O: 100 mg/mL, clear to slightly hazy, colorless to faintly yellow

cation traces

K: 20.3-26.2% (dry basis)

storage temp.

−20°C

Quality Level

200

Categorías relacionadas

Biochemicals

Carbohydrates for Biochemical Research

Cell Culture Supplements & Reagents

Chemical Biology

Chemistry & Biochemicals

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Este artículo	F3627	D3126	P7877
Sigma-Aldrich F1502 D-Fructose 6-phosphate dipotassium salt	Sigma-Aldrich F3627 D-Fructose 6-phosphate disodium salt hydrate	Sigma-Aldrich D3126 2-Deoxyribose 5-phosphate sodium salt	Sigma-Aldrich P7877 6-Phosphogluconic acid trisodium salt
biological source synthetic (inorganic)	biological source bacterial (Corynebacterium)	biological source synthetic (inorganic)	biological source synthetic (organic)
assay ≥97% (enzymatic)	assay ≥98%	assay ≥95% (ICP-AES)	assay ≥97% (enzymatic)
Quality Level 200	Quality Level 300	Quality Level 200	Quality Level 200
solubility H₂O: 100 mg/mL, clear to slightly hazy, colorless to faintly yellow	solubility H₂O: 100 mg/mL, clear to slightly hazy, colorless to faintly yellow	solubility H₂O: 100 mg/mL, clear, colorless to very faintly yellow	solubility water: 50 mg/mL, clear, colorless
form amorphous powder	form amorphous powder	form powder	form powder
storage temp. −20°C	storage temp. −20°C	storage temp. −20°C	storage temp. −20°C

Application

D-Fructose 6-phosphate (F6P) is a sugar intermediate of the glycolytic pathway that may be used to help identify, differentiate and characterize enzymes such as phosphofructokinase(s), pyrophosphate-dependent fructose-6-phosphate 1-phosphotransferase(s), D-fructose-6-phosphate aldolase(s), glutamine:fructose-6-phosphate amino-transferase(s) and glucosamine-6P synthase(s).[1]

Other Notes

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

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Subunit interactions in pig-kidney fructose-1,6-bisphosphatase: binding of substrate induces a second class of site with lowered affinity and catalytic activity.

Joel L Asenjo et al.

Biochimica et biophysica acta, 1840(6), 1798-1807 (2014-01-22)

Fructose-1,6-bisphosphatase, a major enzyme of gluconeogenesis, is inhibited by AMP, Fru-2,6-P2 and by high concentrations of its substrate Fru-1,6-P2. The mechanism that produces substrate inhibition continues to be obscure. Four types of experiments were used to shed light on this:

In vitro characterization of LmbK and LmbO: identification of GDP-D-erythro-α-D-gluco-octose as a key intermediate in lincomycin A biosynthesis.

Chia-I Lin et al.

Journal of the American Chemical Society, 136(3), 906-909 (2014-01-02)

Lincomycin A is a clinically useful antibiotic isolated from Streptomyces lincolnensis. It contains an unusual methylmercapto-substituted octose, methylthiolincosamide (MTL). While it has been demonstrated that the C8 backbone of MTL moiety is derived from D-fructose 6-phosphate and D-ribose 5-phosphate via

Discovery of 1-arylcarbonyl-6,7-dimethoxyisoquinoline derivatives as glutamine fructose-6-phosphate amidotransferase (GFAT) inhibitors.

Yimin Qian et al.

Bioorganic & medicinal chemistry letters, 21(21), 6264-6269 (2011-10-01)

Through high throughput screening and subsequent hit identification and optimization, we synthesized a series of 1-arylcarbonyl-6,7-dimethoxyisoquinoline derivatives as the first reported potent and reversible GFAT inhibitors. SAR studies of this class of compounds indicated significant impact on GFAT inhibition potency

Kinetic characterization of human glutamine-fructose-6-phosphate amidotransferase I: potent feedback inhibition by glucosamine 6-phosphate.

Kay O Broschat et al.

The Journal of biological chemistry, 277(17), 14764-14770 (2002-02-14)

Glutamine-fructose-6-phosphate amidotransferase (GFAT) catalyzes the first committed step in the pathway for biosynthesis of hexosamines in mammals. A member of the N-terminal nucleophile class of amidotransferases, GFAT transfers the amino group from the L-glutamine amide to D-fructose 6-phosphate, producing glutamic

HAD hydrolase function unveiled by substrate screening: enzymatic characterization of Arabidopsis thaliana subclass I phosphosugar phosphatase AtSgpp.

José A Caparrós-Martín et al.

Planta, 237(4), 943-954 (2012-11-28)

This work presents the isolation and the biochemical characterization of the Arabidopsis thaliana gene AtSgpp. This gene shows homology with the Arabidopsis low molecular weight phosphatases AtGpp1 and AtGpp2 and the yeast counterpart GPP1 and GPP2, which have a high

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