Abstract
We have recently shown that adenosine and some of its analogs decrease phosphoribosylpyrophosphate (PP-ribose-P) availability in rat liver cells (unpublished results). Tubercidin (7-deazaadenosine), 3′-deoxyadenosine, and 6-methylmercaptopurine ribonucleoside are the analogs which cause the greatest decrease of PP-ribose-P availability. They are three- to eight-times more potent than adenosine. This action could possibly result from the inhibition of PP-ribose-P synthesis by these compounds or one of their metabolites.
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References
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© 1984 Plenum Press, New York
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Lalanne, M. (1984). Optimal Conditions for Phosphoribosylpyrophosphate Synthesis in a Crude Extract of Liver Cells. In: De Bruyn, C.H.M.M., Simmonds, H.A., Müller, M.M. (eds) Purine Metabolism in Man-IV. Advances in Experimental Medicine and Biology, vol 165. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-4553-4_51
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DOI: https://doi.org/10.1007/978-1-4684-4553-4_51
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4684-4555-8
Online ISBN: 978-1-4684-4553-4
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