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Current Medicinal Chemistry

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Review Article

Sugar-Derived Amidines and Congeners: Structures, Glycosidase Inhibition and Applications

Author(s): Yves Blériot*, Nicolas Auberger and Jérôme Désiré

Volume 29, Issue 7, 2022

Published on: 11 February, 2022

Page: [1271 - 1292] Pages: 22

DOI: 10.2174/0929867329666211222164545

Price: $65

Abstract

Glycosidases, the enzymes responsible for the breakdown of glycoconjugates, including di-, oligo- and polysaccharides, are present across all kingdoms of life. The extreme chemical stability of the glycosidic bond combined with the catalytic rates achieved by glycosidases makes them among the most proficient of all enzymes. Given their multitude of roles in vivo, inhibition of these enzymes is highly attractive with potential in the treatment of a vast array of pathologies ranging from lysosomal storage and diabetes to viral infections. Therefore great efforts have been invested in the last three decades to design and synthesize inhibitors of glycosidases leading to a number of drugs currently on the market. Amongst the vast array of structures that have been disclosed, sugars incorporating an amidine moiety have been the focus of many research groups around the world because of their glycosidase transition state-like structure. In this review, we report and discuss the structure, the inhibition profile, and the use of these molecules, including related structural congeners as transition state analogs.

Keywords: Glycosidase, inhibitor, transition state, amidine, oxocarbenium, enzymes.

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