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Sigma-Aldrich

D-Ribulose solution

~1 M in H2O, ≥97.0% (HPLC)

Synonyme(s) :

D-erythro-2-Ketopentose solution, D-erythro-2-Pentulose solution, D-Adonose solution, D-Arabinulose solution, D-Araboketose solution, D-Erythropentulose solution

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About This Item

Formule empirique (notation de Hill):
C5H10O5
Numéro CAS:
Poids moléculaire :
150.13
Numéro MDL:
Code UNSPSC :
12352204
ID de substance PubChem :
Nomenclature NACRES :
NA.32

Pureté

≥97.0% (HPLC)

Forme

liquid

Concentration

~1 M in H2O

Couleur

colorless

Température de stockage

2-8°C

Chaîne SMILES 

OCC1(O)OC[C@@H](O)[C@H]1O

InChI

1S/C5H10O5/c6-2-5(9)4(8)3(7)1-10-5/h3-4,6-9H,1-2H2/t3-,4-,5?/m1/s1

Clé InChI

LQXVFWRQNMEDEE-ZZKAVYKESA-N

Actions biochimiques/physiologiques

D-Ribulose is a metabolite in pentose and glucuronate interconversions. It plays a role in the D-arabitol production from U. fabae. Ribulose is a rare aldopentose that might show antitumoral and antiviral activities. It acts as a substrate for nicotinamide adenine dinucleotide phosphate (NADP+)-dependent D-arabitol dehydrogenase (ARD1p) enzyme and D-tagatose-3-epimerase from Rhodobacter sphaeroides. Its monophosphate D-ribulose 5-phosphate is an intermediate in the pentose phosphate pathway of glycolysis. D-Ribulose may be found in plants like algae, sugar beet leaves, and barley seed leaves.

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Autres remarques

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

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Tomás Pluskal et al.
Molecular bioSystems, 6(1), 182-198 (2009-12-22)
Metabolomics is a rapidly growing branch of post-genomic chemical biology. The fission yeast Schizosaccharomyces pombe is an excellent eukaryotic model organism. Although the entire S. pombe genome has been sequenced and detailed transcriptomic analyses were performed, little metabolic profiling has
Geeta Meher et al.
Carbohydrate research, 346(6), 703-707 (2011-03-15)
A significant improvement in the production of l-ribulose from inexpensive and commercially available starting materials, L-arabinose and sodium aluminate, is demonstrated. This has facilitated expeditious access to gram-scale quantities of L-ribulofuranoside derivatives.
Tobias Link et al.
The Biochemical journal, 389(Pt 2), 289-295 (2005-03-31)
We have identified and characterized a novel NADP(+)-dependent D-arabitol dehydrogenase and the corresponding gene from the rust fungus Uromyces fabae, a biotrophic plant pathogen on broad bean (Vicia faba). The new enzyme was termed ARD1p (D-arabitol dehydrogenase 1). It recognizes
Longtao Zhang et al.
Biotechnology letters, 31(6), 857-862 (2009-02-12)
A non-characterized gene, previously proposed as the D-tagatose-3-epimerase gene from Rhodobacter sphaeroides, was cloned and expressed in Escherichia coli. Its molecular mass was estimated to be 64 kDa with two identical subunits. The enzyme specificity was highest with D-fructose and
Muhammad Waheed Iqbal et al.
Enzyme and microbial technology, 131, 109427-109427 (2019-10-17)
d-Ribulose and l-fuculose are potentially valuable rare sugars useful for anticancer and antiviral drugs in the agriculture and medicine industries. These rare sugars are usually produced by chemical methods, which are generally expensive, complicated and do not meet the increasing

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