Molecular structure of D-(−)-Arabinose, CAS Number: 10323-20-3
D-(−)-Arabinose (CAS 10323-20-3)
Alternate Names:
D-Arabinose
Application:
D-(−)-Arabinose is a pentose analog of D-ribose
CAS Number:
10323-20-3
Purity:
≥99%
Molecular Weight:
150.13
Molecular Formula:
C5H10O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
D-Arabinose is a pentose sugar that functions as a carbon source in various experimental applications. It is commonly used as a substrate for the enzymatic synthesis of nucleotides and nucleic acids. D-Arabinose is known to inhibit the expression of certain genes in bacterial cells by binding to regulatory proteins, thereby preventing their interaction with DNA. This mechanism of action makes it a useful tool for studying gene regulation and expression in molecular biology research. Additionally, D-Arabinose has been shown to modulate the activity of certain metabolic pathways in bacteria, making it a valuable compound for investigating cellular metabolism and biochemistry. Its ability to specifically interact with cellular components at the molecular level makes it an important reagent in various experimental applications.
D-(−)-Arabinose (CAS 10323-20-3) References
- Molecular and crystal structures of N-arylglycopyranosylamines formed by reaction between sulfanilamide and D-ribose, D-arabinose and D-mannose. | Ojala, CR., et al. 2001. Carbohydr Res. 331: 319-25. PMID: 11383901
- Biosynthesis of d-arabinose in Mycobacterium smegmatis: specific labeling from d-glucose. | Klutts, JS., et al. 2002. Arch Biochem Biophys. 398: 229-39. PMID: 11831854
- Palladium(II) complexes of the reducing sugars D-arabinose, D-ribose, rac-mannose, and D-galactose. | Klüfers, P. and Kunte, T. 2003. Chemistry. 9: 2013-8. PMID: 12740848
- NAD+-specific D-arabinose dehydrogenase and its contribution to erythroascorbic acid production in Saccharomyces cerevisiae. | Amako, K., et al. 2006. FEBS Lett. 580: 6428-34. PMID: 17097644
- Novel substrate specificity of D-arabinose isomerase from Klebsiella pneumoniae and its application to production of D-altrose from D-psicose. | Menavuvu, BT., et al. 2006. J Biosci Bioeng. 102: 436-41. PMID: 17189171
- Preparation of nucleosides derived from 2-nitroimidazole and D-arabinose, D-ribose, and D-galactose by the Vorbrüggen method and their conversion to potential precursors for tracers to image hypoxia. | Schweifer, A. and Hammerschmidt, F. 2011. J Org Chem. 76: 8159-67. PMID: 21905640
- The Effect of D-(-)-arabinose on Tyrosinase: An Integrated Study Using Computational Simulation and Inhibition Kinetics. | Liu, HJ., et al. 2012. Enzyme Res. 2012: 731427. PMID: 23365724
- Novel monosaccharide fermentation products in Caldicellulosiruptor saccharolyticus identified using NMR spectroscopy. | Isern, NG., et al. 2013. Biotechnol Biofuels. 6: 47. PMID: 23552326
- Estimation of D-Arabinose by Gas Chromatography/Mass Spectrometry as Surrogate for Mycobacterial Lipoarabinomannan in Human Urine. | De, P., et al. 2015. PLoS One. 10: e0144088. PMID: 26633829
- Growth inhibitory effect of D-arabinose against the nematode Caenorhabditis elegans: Discovery of a novel bioactive monosaccharide. | Sakoguchi, H., et al. 2016. Bioorg Med Chem Lett. 26: 726-729. PMID: 26791015
- Identification and characterization of d-arabinose reductase and d-arabinose transporters from Pichia stipitis. | Watanabe, S., et al. 2016. Biosci Biotechnol Biochem. 80: 2151-2158. PMID: 27400037
- Novel non-phosphorylative pathway of pentose metabolism from bacteria. | Watanabe, S., et al. 2019. Sci Rep. 9: 155. PMID: 30655589
- Inhibitory effect of d-arabinose on oral bacteria biofilm formation on titanium discs. | An, SJ., et al. 2022. Anaerobe. 75: 102533. PMID: 35143955
- The Biosynthesis of D-1,2,4-Butanetriol From d-Arabinose With an Engineered Escherichia coli. | Wang, J., et al. 2022. Front Bioeng Biotechnol. 10: 844517. PMID: 35402410
- Rational Mutagenesis in the Lid Domain of Ribokinase from E. coli Results in an Order of Magnitude Increase in Activity towards D-arabinose. | Zayats, EA., et al. 2022. Int J Mol Sci. 23: PMID: 36293391
Activator of:
Thomsen-Friedenreich.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
D-(−)-Arabinose, 25 g | sc-278915B | 25 g | $65.00 | |||
D-(−)-Arabinose, 100 g | sc-278915 | 100 g | $212.00 | |||
D-(−)-Arabinose, 250 g | sc-278915A | 250 g | $332.00 | |||
D-(−)-Arabinose, 1 kg | sc-278915C | 1 kg | $1020.00 | |||
D-(−)-Arabinose, 5 kg | sc-278915D | 5 kg | $3060.00 |