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- W1960854856 abstract "Ten N 1-benzylpyridinium chlorides were prepared and studied as inhibitors of the yeast alcohol dehydrogenase-catalyzed oxidation of ethanol. The inhibitors, although containing a variety of functional groups substituted on the ring, all inhibited this reaction and in each case the inhibition observed was competitive with respect to NAD+. Interactions of these inhibitors with the pyridinium region of the NAD+ binding site was suggested by the competitive nature of the inhibition and the simultaneous bintling of all the inhibitors with adenylic acid. Varying the substituent group on the ring did not alter significantly the binding properties of the N 1-benzyl derivatives except in those cases where charged groups were employed. In comparison to the binding of N 1-benzylnicotinamide chloride, N 1-benzyl-3-carboxyl-pyridinium chloride was demonstrated to be bound more poorly. N 1-Benzyl-3-aminomethylpyridinium chloride, on the other hand, was found to be a better inhibitor than N 1-benzylnicotinamide chloride.ACKNOWLEDGMENT This is contribution 42 from the Department of Biochemistry, The University of Tennessee. The work was supported by Research Grant AM-08812-03 from the United States Public Health Service." @default.
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- W1960854856 date "1968-01-01" @default.
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- W1960854856 title "Inhibition of yeast alcohol dehydrogenase by N1-benzylpyridinium chlorides." @default.
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