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D-Sedoheptulose 7-phosphate lithium salt
≥90% (TLC)
Synonim(y):
D-altro-Heptulose 7-phosphate lithium salt
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About This Item
Wzór empiryczny (zapis Hilla):
C7H15O10P · xLi+
Numer CAS:
Masa cząsteczkowa:
290.16 (free acid basis)
Kod UNSPSC:
12352201
NACRES:
NA.25
Polecane produkty
Poziom jakości
Próba
≥90% (TLC)
Postać
powder
kolor
white to light yellow
temp. przechowywania
−20°C
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
Klucz InChI
JDTUMPKOJBQPKX-GBNDHIKLSA-N
Działania biochem./fizjol.
D-Sedoheptulose 7-phosphate is a metabolite in a number of pathways, e.g. an intermediate in the pentose phosphate pathway, and the carbon fixation in photosynthetic organisms.
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).
Opakowanie
Bottomless glass bottle. Contents are inside inserted fused cone.
Inne uwagi
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
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Kod klasy składowania
11 - Combustible Solids
Klasa zagrożenia wodnego (WGK)
WGK 3
Temperatura zapłonu (°F)
Not applicable
Temperatura zapłonu (°C)
Not applicable
Certyfikaty analizy (CoA)
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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
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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
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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
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