Intramolecular hydride transfer from a 1,4-dihydropyridine to an α-ketoester in aqueous solution. A model for lactate dehydrogenase
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
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4. Models for nicotinamide coenzymes. Isotope effect discrepancies in the reaction of dihydronicotinamides with trifluoroacetophenone are due to adduct formation
5. Structure of the active ternary complex of pig heart lactate dehydrogenase with S-lac-NAD at 2.7 Å resolution
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1. A Model Reaction Assesses Contribution of H-Tunneling and Coupled Motions to Enzyme Catalysis;The Journal of Organic Chemistry;2012-08-09
2. Catalytic Strategy of S-Adenosyl-l-homocysteine Hydrolase: Transition-State Stabilization and the Avoidance of Abortive Reactions;Biochemistry;2003-01-28
3. Solvent isotope effects and the nature of electrophilic catalysis m the action of the lactate dehydrogenase of bacillus stearothermophilus;Bioorganic & Medicinal Chemistry;1994-07
4. 1-Substituted (S)-3-(p-tolyl)sulphinyl-1,4-dihydropyridines: novel NADH model compounds;Journal of the Chemical Society, Chemical Communications;1988
5. Nicotinamide as a Coenzyme. An Evolutionary Model of Catalysis and Some Attempts to Translate Ideas into Testable Chemistry;Redesigning the Molecules of Life;1988
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