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- W1650378596 endingPage "370" @default.
- W1650378596 startingPage "335" @default.
- W1650378596 abstract "This chapter discusses some properties of Schiff bases. The Schiff base may be defined as the imine (III) arising from the condensation of an amine and a carbonyl-containing compound. The versatility of the imine bond in promoting an extraordinary variety of apparently different reactions is of biochemical importance. Imines of many carbonyl compounds promote such reactions, even in the absence of specific enzyme proteins, and their effectiveness is especially pronounced when the imine is conjugated with an electron sink—for example, that provided by pyridoxal 5’-phosphate. Such nonenzymic reactions constitute useful models for the enzymic systems. The protein portion of the enzyme, however, by supplying a specific affinity for the substrate and a variety of additional appropriately placed catalytic functional groups enhances the rates of the nonenzymic reactions by factors as high as 107 or more and imparts reaction specificity to the system." @default.
- W1650378596 created "2016-06-24" @default.
- W1650378596 creator A5020771608 @default.
- W1650378596 creator A5080809708 @default.
- W1650378596 date "1970-01-01" @default.
- W1650378596 modified "2023-10-13" @default.
- W1650378596 title "7 Schiff Base Intermediates in Enzyme Catalysis" @default.
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