SMB00918
Arabinofuranose
≥95% (HPLC)
Synonym(s):
L-Arabinofuranose, (3R,4R,5S)-5-(hydroxymethyl)oxolane-2,3,4-triol
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About This Item
Empirical Formula (Hill Notation):
C5H10O5
Molecular Weight:
150.13
MDL number:
UNSPSC Code:
12352201
NACRES:
NA.25
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Assay
≥95% (HPLC)
form
powder
color
off-white
mp
118—121 °C
storage temp.
2-8°C
InChI key
HMFHBZSHGGEWLO-HWQSCIPKSA-N
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General description
L-Arabinofuranose is a fundamental pentose sugar with a five-membered ring structure, serving as the mirror-image enantiomer to D-arabinofuranose. It falls within the class of organic compounds known as pentoses, which consist of monosaccharides featuring a carbohydrate structure composed of five carbon atoms.In biochemistry, L-Arabinofuranose plays a vital role in the synthesis of D-ribose, a key molecule in various biochemical pathways, including metabolomics. Additionally, L-Arabinofuranose is abundantly found in the cell walls and intercellular matrix polysaccharides of higher plant species, such as arabinofuranans, highlighting its significance in plant biology and the structural components of plant cells. In biochemical and cell culture studies, L-arabinofuranose can be utilized to investigate a range of biological processes, enabling the exploration of plant cell wall composition, protein glycosylation, and disease modeling, which are essential in metabolomics and drug development research.
Application
L-Arabinofuranose finds application in metabolomics, biochemical, and drug discovery research.
Features and Benefits
High quality compound suitable for multiple research applications
Other Notes
For additional information on our range of Biochemicals, please complete this form.
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Drugs, their targets and the nature and number of drug targets.
Imming, et al.
Nature Reviews Drug Discovery, 5, 821-834 (2007)
John P Overington et al.
Nature reviews. Drug discovery, 5(12), 993-996 (2006-12-02)
For the past decade, the number of molecular targets for approved drugs has been debated. Here, we reconcile apparently contradictory previous reports into a comprehensive survey, and propose a consensus number of current drug targets for all classes of approved
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