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Merck

78832

D-Sedoheptulose 7-phosphate lithium salt

≥90% (TLC)

Synonyme(s) :

D-altro-Heptulose 7-phosphate lithium salt

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A propos de cet article

Formule empirique (notation de Hill) :
C7H15O10P · xLi+
Numéro CAS:
2646-35-7
Poids moléculaire :
290.16 (free acid basis)
MDL number:
MFCD00057480
UNSPSC Code:
12352201
NACRES:
NA.25

Principaux documents

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Nom du produit

D-Sedoheptulose 7-phosphate lithium salt, ≥90% (TLC)

SMILES string

[P](=O)(OC[C@@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(=O)CO)(O)O

InChI

1S/C7H15O10P/c8-1-3(9)5(11)7(13)6(12)4(10)2-17-18(14,15)16/h4-8,10-13H,1-2H2,(H2,14,15,16)/t4-,5-,6-,7+/m1/s1

InChI key

JDTUMPKOJBQPKX-GBNDHIKLSA-N

assay

≥90% (TLC)

form

powder

color

white to light yellow

storage temp.

−20°C

Quality Level

100

Catégories apparentées

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Cet article
374429203450661
D-Sedoheptulose 7-phosphate lithium salt ≥90% (TLC)

Sigma-Aldrich

78832

D-Sedoheptulose 7-phosphate lithium salt

Dihydroxyacetone phosphate lithium salt ≥95.0% (TLC)

Sigma-Aldrich

37442

Dihydroxyacetone phosphate lithium salt

sn-Glycerol 1-phosphate lithium salt ≥95.0% (TLC)

Sigma-Aldrich

92034

sn-Glycerol 1-phosphate lithium salt

D-Tagatose 6-phosphate lithium salt ≥95% (TLC)

Sigma-Aldrich

50661

D-Tagatose 6-phosphate lithium salt

assay

≥90% (TLC)

assay

≥95.0% (TLC)

assay

≥95.0% (TLC)

assay

≥95% (TLC)

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

form

powder

form

powder

form

powder

form

-

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

color

white to light yellow

color

-

color

-

color

-

Biochem/physiol Actions

D-Sedoheptulose 7-phosphate is a metabolite in a number of pathways, e.g. an intermediate in the pentose phosphate pathway[1][2], and the carbon fixation in photosynthetic organisms[3].
D-Sedoheptulose is a pentose phosphate pathway (PPP) intermediate. D-Sedoheptulose-7-phosphate contributes to the generation of NADPH and the formation of ribose residues of nucleotide synthesis. Sedoheptulose-7-phosphate levels may be increased in individuals with defects in transaldolase (TALSDO1).

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.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Classe de stockage

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number
BCCL7920
BCCK3494
BCCB7206
BCBW5536
BCBT1886

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Mirjam M C Wamelink et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 823(1), 18-25 (2005-08-02)
We describe a liquid chromatography tandem mass spectrometry (LC-MS/MS) method to quantify pentose phosphate pathway intermediates (triose-3-phosphates, tetrose-4-phosphate, pentose-5-phosphate, pentulose-5-phosphates, hexose-6-phosphates and sedoheptulose-7-phosphate (sed-7P)) in bloodspots, fibroblasts and lymphoblasts. Liquid chromatography was performed using an ion pair loaded C(18) HPLC
Biosynthesis of 4-hydroxy-2(or 5)-ethyl-5(or 2)-methyl-3(2H)-furanone by yeasts.
Sasaki, M., et al.
Journal of Agricultural and Food Chemistry, 39, 934-938 (1991)
L Eidels et al.
Proceedings of the National Academy of Sciences of the United States of America, 68(8), 1673-1677 (1971-08-01)
Genetic and biochemical evidence that sedoheptulose-7-phosphate is an obligatory precursor of the L-glycero-D-mannoheptose residues of the lipopolysaccharide of Salmonella was obtained by isolation and characterization of transketolase-negative mutants of Salmonella typhimurium. These mutants, which are defective in synthesis of sedoheptulose-7-phosphate
John F Williams et al.
Photosynthesis research, 90(2), 125-148 (2006-12-13)
14C-Labelled octulose phosphates were formed during photosynthetic 14CO2 fixation and were measured in spinach leaves and chloroplasts. Because mono- and bisphosphates of D: -glycero- D: -ido-octulose are the active 8-carbon ketosugar intermediates of the L-type pentose pathway, it was proposed
Csörsz Nagy et al.
Biochemical Society transactions, 41(2), 674-680 (2013-03-22)
Dynamic carbon re-routing between catabolic and anabolic metabolism is an essential element of cellular transformation associated with tumour formation and immune cell activation. Such bioenergetic adaptations are important for cellular function and therefore require tight control. Carbohydrate phosphorylation has been
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