Abstract
9-(S)-(2,3-Dihydroxypropyl)adenine, a nucleoside analogue with antiviral activity, inhibits the hydrolysis of S-adenosyl-L-homocysteine catalyzed by rat liver S-adenosyl-L-homocysteine hydrolase (Ki = 3.5 μM; Ki/Km = 5.6 . 10-2). The effect upon the synthesis of the substrate is much less pronounced.

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