Antibiotics
(Sep 2020)
Indoline-6-Sulfonamide Inhibitors of the Bacterial Enzyme DapE
Cory T. Reidl,
Tahirah K. Heath,
Iman Darwish,
Rachel M. Torrez,
Maxwell Moore,
Elliot Gild,
Boguslaw P. Nocek,
Anna Starus,
Richard C. Holz,
Daniel P. Becker
Affiliations
Cory T. Reidl
Department of Chemistry and Biochemistry, Loyola University Chicago, 1032 West Sheridan Road, Chicago, IL 60660, USA
Tahirah K. Heath
Department of Chemistry and Biochemistry, Loyola University Chicago, 1032 West Sheridan Road, Chicago, IL 60660, USA
Iman Darwish
Department of Chemistry and Biochemistry, Loyola University Chicago, 1032 West Sheridan Road, Chicago, IL 60660, USA
Rachel M. Torrez
Department of Chemistry and Biochemistry, Loyola University Chicago, 1032 West Sheridan Road, Chicago, IL 60660, USA
Maxwell Moore
Department of Chemistry and Biochemistry, Loyola University Chicago, 1032 West Sheridan Road, Chicago, IL 60660, USA
Elliot Gild
Department of Chemistry and Biochemistry, Loyola University Chicago, 1032 West Sheridan Road, Chicago, IL 60660, USA
Boguslaw P. Nocek
Midwest Center for Structural Genomics and Structural Biology Center, Biosciences Division, Argonne National Laboratory, Argonne, IL 60439, USA
Anna Starus
Department of Chemistry and Biochemistry, Loyola University Chicago, 1032 West Sheridan Road, Chicago, IL 60660, USA
Richard C. Holz
Department of Chemistry, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401, USA
Daniel P. Becker
Department of Chemistry and Biochemistry, Loyola University Chicago, 1032 West Sheridan Road, Chicago, IL 60660, USA
DOI
https://doi.org/10.3390/antibiotics9090595
Journal volume & issue
Vol. 9,
no. 9
p.
595
Abstract
Read online
Inhibitors of the bacterial enzyme dapE-encoded N-succinyl-l,l-diaminopimelic acid desuccinylase (DapE; EC 3.5.1.18) hold promise as antibiotics with a new mechanism of action. Herein we describe the discovery of a new series of indoline sulfonamide DapE inhibitors from a high-throughput screen and the synthesis of a series of analogs. Inhibitory potency was measured by a ninhydrin-based DapE assay recently developed by our group. Molecular docking experiments suggest active site binding with the sulfonamide acting as a zinc-binding group (ZBG).
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