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This work represents part of an ongoing interest within AgrEvo in using mechanism-based biochemical reasoning to generate leads for the disccovery of new agrochemicals. For other recent examples see Dancer, J.E.; Ford, M.J.; Hamilton, K.; Kilkelly, M.; Lindell S.D.; O'Mahony, M.J.; Saville-Stones, E.A. Bioorg. Med. Chem. Lett., 1996, 6, 2131.
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We wish to thank Glaxo Group Research, Greenford for supplying us with a sample of aristeromycin. Formycins A and B were purchased from the Sigma Chemical Company.
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18
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37049132566
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m 35 μM, [adenosine]= 60 μM).
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-1 more favourable than hydration of nebularine 5′-monophosphate (5).
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26
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0032522283
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A similar explanation has been proposed to account for the enhanced binding of 8-azapurine riboside (compared with nebularine) to the enzyme adenosine deaminase: Erion, M.D.; Reddy, M.R. J. Am. Chem. Soc., 1998, 120, 3295.
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