78832
D-Sedoheptulose 7-phosphate lithium salt
≥90% (TLC)
Synonym(s):
D-altro-Heptulose 7-phosphate lithium salt
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1 MG
CZK 5,940.00
5 MG
CZK 20,900.00
About This Item
Empirical Formula (Hill Notation):
C7H15O10P · xLi+
CAS Number:
Molecular Weight:
290.16 (free acid basis)
MDL number:
UNSPSC Code:
12352201
NACRES:
NA.25
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Product Name
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
1 of 4
This Item | 37442 | 92034 | 50661 |
|---|---|---|---|
| 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.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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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
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
Sedoheptulose kinase regulates cellular carbohydrate metabolism by sedoheptulose 7-phosphate supply.
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
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)
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