
Journal of the American Chemical Society p. 3344 - 3353 (1984)
Update date:2022-08-05
Topics:
Freudenreich, Charles
Samama, Jean-Pierre
Biellmann, Jean-Francois
Inhibitors of liver alcohol dehydrogenase were designed from the three-dimensional structure of the enzyme.The ligand to the catalytic zinc ion is an amide group or, better, a formamide group.With the latter function, a hydrogen bond between the NH group and the hydroxyl group of Ser-48 may be formed.The hydrophobic substrate binding site brings structural restraints. α-ω bifunctional molecules show good inhibitory properties possibly due to the interactions with polar residues at the entrance of the substrate binding site.
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Doi:10.1021/jo00187a010
(1984)Doi:10.1016/S0022-328X(00)99189-7
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