5'-Deoxy-5'-fluoroadenosine
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Names | |
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IUPAC name
5’-Deoxy-5’-fluoroadenosine
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Identifiers | |
ChemSpider | 395211 |
Jmol 3D model | Interactive image |
PubChem | 448403 |
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Properties | |
C10H12FN5O3 | |
Molar mass | 269.24 g·mol−1 |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references | |
5'-Deoxy-5'-fluoroadenosine is the first step in the biosynthesis of organic fluorides. It is synthesized by the fluorinase catalyzed addition of a fluoride ion to S-adenosyl-L-methionine, releasing L-methionine as a by product.[1] Purine nucleoside phosphorylase mediates a phosphorolytic cleavage of the adenine base to generate 5-fluoro-5-deoxy-D-ribose-1-phosphate.
References
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