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An empirical study of amide–heteroarene π-stacking interactions using reversible inhibitors of a bacterial serine hydrolase

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Abstract

Compared to aryl–aryl π-stacking interactions, the analogous stacking of heteroarenes on amide π systems is less well understood and vastly underutilized in structure-based drug design. Recent theoretical studies have delineated the important geometric coordinates of the interaction, some of which have been confirmed with synthetic model systems based on Rebek imides. Unfortunately, a broadly useful and tractable protein–ligand model system of this interaction has remained elusive. Here we employed a known inhibitor scaffold to study π-stacking of diverse heteroarene substituents on the amide face of Gly238 in the cephalosporinases CTX-M-14 and CTX-M-27. Biochemical inhibition constants (Ki) and biophysical binding constants (Kd) were determined for nineteen new analogues against both enzymes, while multiple high-resolution co-crystal structures revealed remarkably consistent placement of the probe heteroarene on Gly238. The data presented support the predicted importance of opposing dipoles in amide–heteroarene interactions and should be useful for evaluating other theoretical predictions concerning these interactions.

Graphical abstract: An empirical study of amide–heteroarene π-stacking interactions using reversible inhibitors of a bacterial serine hydrolase

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Publication details

The article was received on 07 Mar 2019, accepted on 06 May 2019 and first published on 15 May 2019


Article type: Research Article
DOI: 10.1039/C9QO00342H
Org. Chem. Front., 2019, Advance Article

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    An empirical study of amide–heteroarene π-stacking interactions using reversible inhibitors of a bacterial serine hydrolase

    K. DeFrees, M. T. Kemp, X. ElHilali-Pollard, X. Zhang, A. Mohamed, Y. Chen and A. R. Renslo, Org. Chem. Front., 2019, Advance Article , DOI: 10.1039/C9QO00342H

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