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83870

Sigma-Aldrich

D-Ribose 5-phosphate barium salt hexahydrate

≥99.0% (TLC)

Synonym(s):

R-5-P-Ba

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About This Item

Empirical Formula (Hill Notation):
C5H9BaO8P · 6H2O
CAS Number:
15673-79-7
Molecular Weight:
473.51
Beilstein:
3781061
EC Number:
239-750-0
MDL number:
MFCD00149441
UNSPSC Code:
12352201
PubChem Substance ID:
57652972
NACRES:
NA.25

Assay

≥99.0% (TLC)

form

powder

optical activity

[α]20/D +12±2°, c = 1% in 0.2 M HCl

storage temp.

2-8°C

SMILES string

[Ba++].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]C(=O)[C@H](O)[C@H](O)[C@H](O)COP([O-])([O-])=O

InChI

1S/C5H11O8P.Ba.6H2O/c6-1-3(7)5(9)4(8)2-13-14(10,11)12;;;;;;;/h1,3-5,7-9H,2H2,(H2,10,11,12);;6*1H2/q;+2;;;;;;/p-2/t3-,4+,5-;;;;;;;/m0......./s1

InChI key

WUZJSCGFQURQNK-BJLVBTRRSA-L

Related Categories

Application

D-Ribose 5-phosphate is used as a substrate to identify, differentiate and characterize ribose-5-phosphate isomerase(s) and phosphopentomutase(s). Ribose 5-phosphate is used to study the processes and effects of glycation in vivo and in vitro.

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302 + H332

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Michelle F Clasquin et al.
Cell, 145(6), 969-980 (2011-06-15)
Glucose is catabolized in yeast via two fundamental routes, glycolysis and the oxidative pentose phosphate pathway, which produces NADPH and the essential nucleotide component ribose-5-phosphate. Here, we describe riboneogenesis, a thermodynamically driven pathway that converts glycolytic intermediates into ribose-5-phosphate without
Rebecca A Gersten et al.
Carbohydrate research, 345(17), 2499-2506 (2010-10-12)
Ribose 5-phosphate (R5P) is a sugar known to undergo the Maillard reaction (glycation) at a rapid rate. In a reaction with the lysines of bovine heart cytochrome c, R5P generates superoxide (O2-) that subsequently reduces ferri-cytochrome c to ferro-cytochrome c.
Luke J Alderwick et al.
Glycobiology, 21(4), 410-425 (2010-11-04)
Mycobacterium tuberculosis arabinogalactan (AG) is an essential cell wall component. It provides a molecular framework serving to connect peptidoglycan to the outer mycolic acid layer. The biosynthesis of the arabinan domains of AG and lipoarabinomannan (LAM) occurs via a combination
Bianca Derrer et al.
FEBS letters, 584(19), 4169-4174 (2010-09-15)
Most organisms synthesise the B(6) vitamer pyridoxal 5-phosphate (PLP) via the glutamine amidotransferase PLP synthase, a large enzyme complex of 12 Pdx1 synthase subunits with up to 12 Pdx2 glutaminase subunits attached. Deletion analysis revealed that the C-terminus has four
L E Meshalkina et al.
Biochemistry. Biokhimiia, 76(9), 1061-1064 (2011-11-16)
The Michaelis constant values for substrates of transketolase from human tissues were determined over a wide range of substrate concentrations. It is shown that K(m) values determined by other authors are significantly overestimated and explained why this is so.
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