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

5-Fluoro-5-deoxy-d-ribose 1-phosphate
Names
	IUPAC name 5-Deoxy-5-fluoro-1-O-phosphonato-d-ribofuranose
Identifiers
3D model (JSmol)	Interactive image;
ChemSpider	21169315 (dianion);
PubChem CID	49859615 (dianion);
	SMILES O[C@@H]1[C@H](O)[C@@H](CF)OC1OP(=O)(O)O;
Properties
Chemical formula	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.[1] It is isomerized to 5-fluoro-5-deoxy-ribulose-1-phosphate which is then cleaved by an aldolase to release fluoroacetaldehyde.[2]

References

O'Hagan D; Schaffrath C; Cobb SL; Hamilton JT; Murphy CD (2002). "Biochemistry: biosynthesis of an organofluorine molecule". Nature. 416 (6878): 279. doi:10.1038/416279a. PMID 11907567.
Hai Deng; Stuart M. Cross; Ryan P. McGlinchey; John T.G. Hamilton; David O'Hagan (2008). "In Vitro Reconstituted Biotransformation of 4-Fluorothreonine from Fluoride Ion: Application of the Fluorinase". Chemistry and Biology. 15 (12): 1268–1276. doi:10.1016/j.chembiol.2008.10.012. PMID 19101471.

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[1] O'Hagan D; Schaffrath C; Cobb SL; Hamilton JT; Murphy CD (2002). "Biochemistry: biosynthesis of an organofluorine molecule". Nature. 416 (6878): 279. doi:10.1038/416279a. PMID 11907567.

[2] Hai Deng; Stuart M. Cross; Ryan P. McGlinchey; John T.G. Hamilton; David O'Hagan (2008). "In Vitro Reconstituted Biotransformation of 4-Fluorothreonine from Fluoride Ion: Application of the Fluorinase". Chemistry and Biology. 15 (12): 1268–1276. doi:10.1016/j.chembiol.2008.10.012. PMID 19101471.