[5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-[hydroxy-(3,4,5-trihydroxyoxan-2-yl)oxy-phosphoryl]oxy-phosphinic acid

Modify Date: 2024-01-03 09:37:20

[5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-[hydroxy-(3,4,5-trihydroxyoxan-2-yl)oxy-phosphoryl]oxy-phosphinic acid Structure
[5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-[hydroxy-(3,4,5-trihydroxyoxan-2-yl)oxy-phosphoryl]oxy-phosphinic acid structure
Common Name [5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-[hydroxy-(3,4,5-trihydroxyoxan-2-yl)oxy-phosphoryl]oxy-phosphinic acid
CAS Number 3616-06-6 Molecular Weight 536.27600
Density N/A Boiling Point N/A
Molecular Formula C14H22N2O16P2 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of [5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-[hydroxy-(3,4,5-trihydroxyoxan-2-yl)oxy-phosphoryl]oxy-phosphinic acid


UDP-xylose is a natural product that could be isolated from Cryptococcus laurentii (NRRL Y-1401). UDP-xylose is a sugar donor for the synthesis of glycoproteins, polysaccharides, various metabolites, and oligosaccharides in plants, vertebrates, and fungi[1][2].

 Names

Name UDP-α-D-xylose
Synonym More Synonyms

  Biological Activity

Description UDP-xylose is a natural product that could be isolated from Cryptococcus laurentii (NRRL Y-1401). UDP-xylose is a sugar donor for the synthesis of glycoproteins, polysaccharides, various metabolites, and oligosaccharides in plants, vertebrates, and fungi[1][2].
Related Catalog
References

[1]. Ankel H, et al. ISOLATION OF UDP-D-XYLOSE FROM CRYPTOCOCCUS LAURENTII (NRRL Y-1401). Biochim Biophys Acta. 1964 Aug 19;90:397-9.  

[2]. Pattathil S, et al. Biosynthesis of UDP-xylose: characterization of membrane-bound AtUxs2. Planta. 2005 Jun;221(4):538-48.  

 Chemical & Physical Properties

Molecular Formula C14H22N2O16P2
Molecular Weight 536.27600
Exact Mass 536.04400
PSA 296.38000
Storage condition -20°C

 Precursor & DownStream

Precursor  0

DownStream  1

 Synonyms

MFCD32644832