5-Fluoro-5-deoxy-D-ribose 1-phosphate

5-Fluoro-5-deoxy-D-ribose 1-phosphate
Names
IUPAC name
5-Deoxy-5-fluoro-D-ribofuranosyl dihydrogen phosphate
Preferred IUPAC name
(2Ξ,3R,4S,5S)-5-(Fluoromethyl)-3,4-dihydroxyoxolan-2-yl dihydrogen phosphate
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C5H10FO7P/c6-1-2-3(7)4(8)5(12-2)13-14(9,10)11/h2-5,7-8H,1H2,(H2,9,10,11)/t2-,3-,4-,5?/m1/s1
    Key: LUQFMENCTWEBSQ-SOOFDHNKSA-N
  • O[C@@H]1[C@H](O)[C@@H](CF)OC1OP(=O)(O)O
Properties
C5H10FO7P
Molar mass 232.100 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

5-Fluoro-5-deoxy-D-ribose 1-phosphate is metabolite formed during the biosynthesis of organofluorides. It is formed by the purine nucleoside phosphorylase mediated phosphorolytic cleavage of 5'-deoxy-5'-fluoroadenosine. It is isomerized to 5-fluoro-5-deoxy-ribulose-1-phosphate which is then cleaved by an aldolase to release fluoroacetaldehyde.

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