Issue 20, 2015

Galacto configured N-aminoaziridines: a new type of irreversible inhibitor of β-galactosidases

Abstract

A new type of galactose mimetics has been synthesized following a straightforward synthetic approach based on cyclohexene olefin aziridination reactions directed by hydroxyl substituents. These enantiomerically pure galacto-configured N-aminoaziridines are potent irreversible inhibitors of Aspergillus oryzae and Escherichia coli β-galactosidases.

Graphical abstract: Galacto configured N-aminoaziridines: a new type of irreversible inhibitor of β-galactosidases

Supplementary files

Article information

Article type
Paper
Submitted
17 Mar 2015
Accepted
10 Apr 2015
First published
10 Apr 2015

Org. Biomol. Chem., 2015,13, 5690-5697

Author version available

Galacto configured N-aminoaziridines: a new type of irreversible inhibitor of β-galactosidases

A. Alcaide, A. Trapero, Y. Pérez and A. Llebaria, Org. Biomol. Chem., 2015, 13, 5690 DOI: 10.1039/C5OB00532A

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