Repurposing the Antihistamine Terfenadine for Antimicrobial Activity against Staphylococcus aureus
Author(s) -
Jessamyn I. Perlmutter,
Lauren Forbes,
Damian J. Krysan,
Katherine Ebsworth-Mojica,
Jennifer M. Colquhoun,
Jenna L. Wang,
Paul M. Dunman,
Daniel P. Flaherty
Publication year - 2014
Publication title -
journal of medicinal chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.01
H-Index - 261
eISSN - 1520-4804
pISSN - 0022-2623
DOI - 10.1021/jm5010682
Subject(s) - terfenadine , staphylococcus aureus , chemistry , antimicrobial , antihistamine , pharmacology , herg , antibiotics , drug repositioning , microbiology and biotechnology , bacteria , drug , medicine , biochemistry , biology , potassium channel , genetics , organic chemistry
Staphylococcus aureus is a rapidly growing health threat in the U.S., with resistance to several commonly prescribed treatments. A high-throughput screen identified the antihistamine terfenadine to possess, previously unreported, antimicrobial activity against S. aureus and other Gram-positive bacteria. In an effort to repurpose this drug, structure-activity relationship studies yielded 84 terfenadine-based analogues with several modifications providing increased activity versus S. aureus and other bacterial pathogens, including Mycobacterium tuberculosis. Mechanism of action studies revealed these compounds to exert their antibacterial effects, at least in part, through inhibition of the bacterial type II topoisomerases. This scaffold suffers from hERG liabilities which were not remedied through this round of optimization; however, given the overall improvement in activity of the set, terfenadine-based analogues provide a novel structural class of antimicrobial compounds with potential for further characterization as part of the continuing process to meet the current need for new antibiotics.
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